ascopubs.org Open in urlscan Pro
104.18.0.170  Public Scan

URL: https://ascopubs.org/doi/full/10.1200/JCO.22.01357
Submission: On October 03 via manual from US — Scanned from DE

Form analysis 17 forms found in the DOM

Name: quickSearchGET /action/doSearch

<form action="/action/doSearch" name="quickSearch" class="quickSearchForm search-open resQuickSearchForm" title="Quick Search" method="get">
  <div class="container">
    <span class="searchDropDownDivLeft">
      <label for="searchInSelector" class="visuallyhidden">Search in:</label>
      <select id="searchInSelector" name="SeriesKey" class="custom-dropdown js__searchInSelector">
        <option value="jco" id="thisJournal" data-search-in="thisJournal"> Search This Journal </option>
        <option value="" data-search-in="default">Search ASCO Journals</option>
      </select>
    </span>
    <div class="quicksearch-container">
      <span class="citationSearchBoxContainer hidden">
        <input name="quickLinkJournal" class="journalName mediumTextInput textIndent autocomplete ui-autocomplete-input" value="Journal of Clinical Oncology" type="text" title="Journal" placeholder="Journal" autocomplete="off" autopopulate="true"
          data-auto-complete-target="title-auto-complete" data-history-items-conf="3" data-publication-titles-conf="3" data-topics-conf="3" data-contributors-conf="3" disabled="disabled"><span role="status" aria-live="polite"
          class="ui-helper-hidden-accessible"></span>
        <input type="hidden" name="quickLink" value="true" disabled="disabled">
        <input class="year smallTextInput" title="Year" type="text" name="quickLinkYear" value="" size="15" autocomplete="false" placeholder="Year" pattern="([0-9]){1,4}$" disabled="disabled">
        <input class="volume smallTextInput" title="Volume" type="text" name="quickLinkVolume" value="" size="15" autocomplete="false" placeholder="Volume" disabled="disabled">
        <input class="issue smallTextInput enable" title="Issue" type="text" name="quickLinkIssue" value="" size="15" autocomplete="false" placeholder="Issue" disabled="disabled">
        <input class="page smallTextInput" title="Page" type="text" name="quickLinkPage" value="" size="15" autocomplete="false" placeholder="Page" disabled="disabled">
      </span>
      <div class="simpleSearchBoxContainer">
        <input name="AllField" class="searchText magicsuggest main-search-field textIndent autocomplete ui-autocomplete-input" value="" type="search" id="searchText" title="Type search term here"
          placeholder="Enter words / phrases / DOI / ISBN / authors / keywords / etc." autocomplete="off" data-history-items-conf="3" data-publication-titles-conf="3" data-group-titles-conf="3" data-publication-items-conf="3" data-topics-conf="3"
          data-contributors-conf="3" data-display-labels="true" data-fuzzy-suggester="false" data-auto-complete-target="auto-complete" data-auto-complete-max-words="7" data-auto-complete-max-chars="32"><span role="status" aria-live="polite"
          class="ui-helper-hidden-accessible"></span>
        <input name="ConceptID" value="" type="hidden">
      </div>
      <div class="quicksearch-actions">
        <input class="mainSearchButton searchButtons pointer" title="search" type="submit" value="Search">
        <a class="responsiveAdvanceSearch" href="/search/advanced" title="Advanced Search">
                            <span class="AdvanceSearch">
                                Advanced Search
                            </span>
                            <span class="hidden-xs hidden-sm icon-advanced_search"></span>
                        </a>
      </div>
    </div>
  </div>
</form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="">Abstract &lt;&lt;</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="">INTRODUCTION &lt;&lt;</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="">GUIDELINE QUESTIONS &lt;&lt;</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="">METHODS &lt;&lt;</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="">RESULTS &lt;&lt;</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="">RECOMMENDATIONS &lt;&lt;</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="">EVIDENCE SUMMARY OF INTER... &lt;&lt;</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="">DISCUSSION &lt;&lt;</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="">PATIENT AND CLINICIAN COM... &lt;&lt;</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="">HEALTH DISPARITIES &lt;&lt;</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="">GUIDELINE IMPLEMENTATION ... &lt;&lt;</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="">OPEN COMMENT REVIEW &lt;&lt;</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="">LIMITATIONS OF THE RESEAR... &lt;&lt;</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="">FUTURE DIRECTIONS &lt;&lt;</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="">ADDITIONAL RESOURCES &lt;&lt;</option>
    <option value="#_i125">REFERENCES</option>
  </select></form>

<form style="margin-bottom:0"><select name="select23" class="fulltextdd" onchange="GoTo(this, 'self')">
    <option value="#" selected="#">Choose</option>
    <option value="#">Top of page</option>
    <option value="#abstract">Abstract</option>
    <option value="#_i5">INTRODUCTION</option>
    <option value="#_i32">GUIDELINE QUESTIONS</option>
    <option value="#_i33">METHODS</option>
    <option value="#_i37">RESULTS</option>
    <option value="#_i43">RECOMMENDATIONS</option>
    <option value="#_i83">EVIDENCE SUMMARY OF INTER...</option>
    <option value="#_i107">DISCUSSION</option>
    <option value="#_i108">PATIENT AND CLINICIAN COM...</option>
    <option value="#_i109">HEALTH DISPARITIES</option>
    <option value="#_i110">GUIDELINE IMPLEMENTATION ...</option>
    <option value="#_i111">OPEN COMMENT REVIEW</option>
    <option value="#_i112">LIMITATIONS OF THE RESEAR...</option>
    <option value="#_i113">FUTURE DIRECTIONS</option>
    <option value="#_i114">ADDITIONAL RESOURCES</option>
    <option value="">REFERENCES &lt;&lt;</option>
  </select></form>

Text Content

Skip to main content






Log In
submission complete icon Submit
envelope E-Alerts
cart Cart

OpenAthens/Shibboleth »


Enter words / phrases / DOI / ISBN / authors / keywords / etc.
Search in: Search This Journal Search ASCO Journals
Advanced Search


Menu
 * Newest Content
 * Issues
   * Current Issue
   * Past Issues
 * Special Content
   * ASCO Guidelines
   * Special Series
   * JCO Podcasts
   * Cancer Stories Podcast
   * Meeting Abstracts
   * Oncology Grand Rounds
   * Understanding the Pathway
 * Authors
   * Author Center
   * Open Access Terms
   * Preparing a Manuscript
     * Determine My Article Type
     * Format My Manuscript
     * Submit My Manuscript
     * Contact Editorial
   * What To Expect
     * Peer Review Process
     * My Article Was Accepted
   * Policies and Guidelines
     * Journal Policies
     * Embargo Policy
     * Author Promotion Toolkit
   * Resources
     * From the Editors
     * Author FAQ
     * Professional English and Academic Editing Support
   * Submit to JCO
 * Subscribers
   * Subscriber Center
   * Manage Subscription
   * Renew Subscription
   * View/Change User Info
   * Institutions and Librarians
   * Subscribe to this Journal
   * Email Alerts
   * Subscriber FAQ
 * About
   * About JCO
   * Editorial Roster
   * Permissions
   * Reprints
   * Advertising
   * Become a Reviewer
   * Contact Us
 * ASCO Publications
   * Journal of Clinical Oncology
   * JCO Oncology Practice
   * JCO Global Oncology
   * JCO Clinical Cancer Informatics
   * JCO Precision Oncology
   * ASCO Publications Home
 * Career Center
 * COVID-19

Follow @JCO_ASCO on Twitter
Log In

 * >
 * Journal of Clinical Oncology >
 * List of Issues >
 * Newest Content >
 * 

Article Tools


ASCO SPECIAL ARTICLES


ARTICLE TOOLS


OPTIONS & TOOLS

Export Citation Track Citation Add To Favorites

 * Rights & Permissions

Facebook Twitter Email AddThis




COMPANION ARTICLES

No companion articles


ARTICLE CITATION

DOI: 10.1200/JCO.22.01357 Journal of Clinical Oncology - published online before
print September 19, 2022

PMID: 36122322






INTEGRATIVE MEDICINE FOR PAIN MANAGEMENT IN ONCOLOGY: SOCIETY FOR INTEGRATIVE
ONCOLOGY–ASCO GUIDELINE



Jun J. Mao , MD, MSCE1
x
Jun J. Mao
Search for articles by this author



; Nofisat Ismaila , MD, MSc2
x
Nofisat Ismaila
Search for articles by this author



; Ting Bao , MD1
x
Ting Bao
Search for articles by this author



; Debra Barton , PhD3
x
Debra Barton
Search for articles by this author



; Eran Ben-Arye , MD4
x
Eran Ben-Arye
Search for articles by this author



; Eric L. Garland, PhD5
x
Eric L. Garland
Search for articles by this author



; ...Heather Greenlee , ND, PhD6
x
Heather Greenlee
Search for articles by this author



; Thomas Leblanc , MD7
x
Thomas Leblanc
Search for articles by this author



; Richard T. Lee , MD8
x
Richard T. Lee
Search for articles by this author



; Ana Maria Lopez , MD9
x
Ana Maria Lopez
Search for articles by this author



; Charles Loprinzi , MD10
x
Charles Loprinzi
Search for articles by this author



; Gary H. Lyman , MD, MPH6
x
Gary H. Lyman
Search for articles by this author



; Jodi MacLeod , BA11
x
Jodi MacLeod
Search for articles by this author



; Viraj A. Master, MD, PhD12
x
Viraj A. Master
Search for articles by this author



; Kavitha Ramchandran, MD13
x
Kavitha Ramchandran
Search for articles by this author



; Lynne I. Wagner , PhD14
x
Lynne I. Wagner
Search for articles by this author



; Eleanor M. Walker, MD15
x
Eleanor M. Walker
Search for articles by this author



; Deborah Watkins Bruner , PhD12
x
Deborah Watkins Bruner
Search for articles by this author



; Claudia M. Witt , MD, MBA16
x
Claudia M. Witt
Search for articles by this author



; and Eduardo Bruera , MD17
x
Eduardo Bruera
Search for articles by this author



1Memorial Sloan Kettering Cancer Center, New York, NY
2American Society of Clinical Oncology, Alexandria, VA
3University of Michigan School of Nursing, Ann Arbor, MI
4Lin & Carmel Medical Centers, Clalit Health Services; Technion Faculty of
Medicine, Haifa, Israel
5College of Social Work, University of Utah, Salt Lake City, UT
6Fred Hutchinson Cancer Research Center, Seattle, WA
7Duke University School of Medicine Durham, NC
8City of Hope Comprehensive Cancer Center, Duarte, CA
9Thomas Jefferson. Sidney Kimmel Cancer Center, Philadelphia, PA
10Mayo Clinic, Rochester, MN
11Patient Representative, Memorial Sloan Kettering Integrative Medicine Service,
New York, NY
12Winship Cancer Institute of Emory University, Atlanta, GA
13Stanford University, Palo Alto, CA
14Wake Forest School of Medicine, Winston-Salem, NC
15Henry Ford Hospital, Detroit, MI
16University Hospital Zurich, Zurich, Switzerland
17MD Anderson Cancer Center, Houston, TX
Show More

*J.J.M. and E.B. were expert panel cochairs.


https://doi.org/10.1200/JCO.22.01357

 * Abstract
 * Full Text
 * PDF
 * Figures and Tables
 * Supplements

ABSTRACT

Section:
ChooseTop of pageAbstract <<INTRODUCTIONGUIDELINE
QUESTIONSMETHODSRESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF
INTER...DISCUSSIONPATIENT AND CLINICIAN COM...HEALTH DISPARITIESGUIDELINE
IMPLEMENTATION ...OPEN COMMENT REVIEWLIMITATIONS OF THE RESEAR...FUTURE
DIRECTIONSADDITIONAL RESOURCESREFERENCES

PURPOSE


The aim of this joint guideline is to provide evidence-based recommendations to
practicing physicians and other health care providers on integrative approaches
to managing pain in patients with cancer.

METHODS


The Society for Integrative Oncology and ASCO convened an expert panel of
integrative oncology, medical oncology, radiation oncology, surgical oncology,
palliative oncology, social sciences, mind-body medicine, nursing, and patient
advocacy representatives. The literature search included systematic reviews,
meta-analyses, and randomized controlled trials published from 1990 through
2021. Outcomes of interest included pain intensity, symptom relief, and adverse
events. Expert panel members used this evidence and informal consensus to
develop evidence-based guideline recommendations.

RESULTS


The literature search identified 227 relevant studies to inform the evidence
base for this guideline.

RECOMMENDATIONS


Among adult patients, acupuncture should be recommended for aromatase
inhibitor–related joint pain. Acupuncture or reflexology or acupressure may be
recommended for general cancer pain or musculoskeletal pain. Hypnosis may be
recommended to patients who experience procedural pain. Massage may be
recommended to patients experiencing pain during palliative or hospice care.
These recommendations are based on an intermediate level of evidence, benefit
outweighing risk, and with moderate strength of recommendation. The quality of
evidence for other mind-body interventions or natural products for pain is
either low or inconclusive. There is insufficient or inconclusive evidence to
make recommendations for pediatric patients. More research is needed to better
characterize the role of integrative medicine interventions in the care of
patients with cancer.

Additional information is available at
https://integrativeonc.org/practice-guidelines/guidelines and
www.asco.org/survivorship-guidelines.

INTRODUCTION
Section:
ChooseTop of pageAbstractINTRODUCTION <<GUIDELINE
QUESTIONSMETHODSRESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF
INTER...DISCUSSIONPATIENT AND CLINICIAN COM...HEALTH DISPARITIESGUIDELINE
IMPLEMENTATION ...OPEN COMMENT REVIEWLIMITATIONS OF THE RESEAR...FUTURE
DIRECTIONSADDITIONAL RESOURCESREFERENCES


Pain is one of the most common, disabling, and feared symptoms experienced by
patients diagnosed with cancer.1,2 Among patients with advanced cancer, pain can
be a result of tumor burden or invasion of bones, muscles, or nerves. In
addition, many conventional cancer treatments such as surgery, chemotherapy,
radiotherapy, immunotherapy, or hormonal therapy can result in both acute and
chronic pain conditions such as aromatase inhibitor (AI)–induced joint pain or
chemotherapy-induced peripheral neuropathy (CIPN) pain.3,4 With improved
oncologic treatment, many patients diagnosed with advanced cancer now live
longer with symptomatic illness and ongoing oncologic treatment. Additionally,
increasing numbers of patients experience remission and join the 16.9 million
cancer survivors in the United States alone.5 Many survivors, however, continue
to experience chronic pain resulting from their cancer treatment that not only
negatively affects their quality of life, but also their daily functions.6
Chronic pain may also lead to nonadherence to oncologic treatment such as
hormonal therapies,7,8 thus, potentially compromising overall survival.
Therefore, effective pain management is of critical importance throughout the
cancer care trajectory.

THE BOTTOM LINE

Integrative Medicine for Pain Management in Oncology: Society for Integrative
Oncology—ASCO Guideline

Guideline Questions



 1. What mind-body therapies are recommended for managing pain experienced by
    adult and pediatric patients diagnosed with cancer?

 2. What natural products are recommended for managing pain experienced by adult
    and pediatric patients diagnosed with cancer?



Target Population

Patients of any age diagnosed with any cancer who are experiencing pain during
any stage of their cancer care trajectory.

Target Audience

Clinicians who provide care to patients with cancer, cancer survivors, and
family caregivers.

Methods

An Expert Panel was convened to develop clinical practice guideline
recommendations on the basis of a systematic review of the health literature.

Recommendations

The following recommendations are evidence-based, informed by randomized trials
and systematic reviews, and guided by clinical experience. The recommendations
were developed by a multidisciplinary group of experts.

NOTE:

The following set of recommendations are for adults with cancer. Although many
of the recommendations are weak and based on low-quality evidence, the
interventions do have clinical relevance, with a favorable benefit-to-harm
ratio, and this is the basis for making the recommendations. There is
insufficient or inconclusive evidence to make recommendations for pediatric
patients with cancer.

Aromatase inhibitor–related joint pain.
Recommendation 1.1.

Acupuncture should be offered to patients experiencing AI-related joint pain in
breast cancer (Type: Evidence based, benefits outweigh harms; Evidence quality:
Intermediate; Strength of recommendation: Moderate).

Recommendation 1.2.

Yoga may be offered to patients experiencing AI-related joint pain in breast
cancer (Type: Evidence based, benefits outweigh harms; Evidence quality: Low;
Strength of recommendation: Weak).

General cancer pain or musculoskeletal pain.
Recommendation 1.3.

Acupuncture may be offered to patients experiencing general pain or
musculoskeletal pain from cancer (Type: Evidence based, benefits outweigh harms;
Evidence quality: Intermediate; Strength of recommendations: Moderate).

Recommendation 1.4.

Reflexology or acupressure may be offered to patients experiencing pain during
systemic therapy for cancer treatment (Type: Evidence based, benefits outweigh
harms; Evidence quality: Intermediate; Strength of recommendation: Moderate).

Recommendation 1.5.

Massage may be offered to patients experiencing chronic pain following breast
cancer treatment (Type: Evidence based, benefits outweigh harms; Evidence
quality: Low; Strength of recommendation: Moderate).

Recommendation 1.6.

Hatha yoga may be offered to patients experiencing pain after treatment for
breast or head and neck cancers (Type: Evidence based, benefits outweigh harms;
Evidence quality: Low; Strength of recommendation: Weak).

Recommendation 1.7.

Guided imagery with progressive muscle relaxation may be offered to patients
experiencing general pain from cancer treatment (Type: Evidence based, benefits
and harms not assessable; Evidence quality: Low; Strength of recommendation:
Weak).

Chemotherapy-induced peripheral neuropathy.
Recommendation 1.8.

Acupuncture may be offered to patients experiencing chemotherapy-induced
peripheral neuropathy from cancer treatment (Type: Evidence based-informal
consensus, benefits outweigh harms; Evidence quality: Low; Strength of
recommendation: Weak).

Recommendation 1.9.

Reflexology or acupressure may be offered to patients experiencing
chemotherapy-induced peripheral neuropathy from cancer treatment (Type: Evidence
based, benefits outweigh harms; Evidence quality: Low; Strength of
recommendation: Weak).

Procedural or surgical pain.
Recommendation 1.10.

Hypnosis may be offered to patients experiencing procedural pain in cancer
treatment or diagnostic workups (Type: Evidence based, benefits outweigh harms;
Evidence quality: Intermediate; Strength of recommendation: Moderate).

Recommendation 1.11.

Acupuncture or acupressure may be offered to patients undergoing cancer surgery
or other cancer-related procedures such as bone marrow biopsy (Type: Evidence
based-informal consensus, benefits outweigh harms; Evidence quality of: Low;
Strength of recommendation: Weak).

Recommendation 1.12.

Music therapy may be offered to patients experiencing surgical pain from cancer
surgery (Type: Evidence based, benefits outweigh harms; Evidence quality of:
Low; Strength of recommendation: Weak).

Pain during palliative care.
Recommendation 1.13.

Massage may be offered to patients experiencing pain during palliative and
hospice care (Type: Evidence based; benefits outweigh harms; Evidence quality:
Intermediate; Strength of recommendation: Moderate).

Please refer to the treatment algorithm in Figure 2 for the visual
representation of these recommendations.

Additional Resources

Definitions for the quality of the evidence and strength of recommendation
ratings are available in Appendix Table A1 (online only). More information,
including a supplement with additional evidence tables, slide sets, and clinical
tools and resources, is available at
https://integrativeonc.org/practice-guidelines/guidelines and
www.asco.org/survivorship-guidelines. The Society for Integrative Oncology
Clinical Practice Guidelines Committee's Standard Operating Procedures
(available at https://integrativeonc.org/practice-guidelines/guidelines-sops)
and the Methodology Manual (available at www.asco.org/guideline-methodology)
provide additional information about the methods used to develop this guideline.
Patient information is available at
https://integrativeonc.org/knowledge-center/patients and www.cancer.net.

Society for Integrative Oncology and ASCO believe that cancer clinical trials
are vital to inform clinical decisions and improve cancer care, and that all
patients should have the opportunity to participate.

As pain in patients and survivors of cancer is complex with different etiologies
(eg, tumor burden, treatment-related, and non–cancer-related) and varying
presentations (eg, neuropathic and musculoskeletal) and duration (eg, acute and
chronic), pain management requires an interdisciplinary approach and should
include both pharmacologic and nonpharmacologic treatments, where appropriate.2
Integrative medicine, defined as the coordinated use of evidence-based
complementary practices and conventional care treatments,9 includes
interventions such as acupuncture, massage, meditation, and yoga, which are
increasingly available in cancer centers and are recommended for symptom and
pain management.10,11 An estimated 40% of patients with cancer use integrative
medicine on an annual basis.12-14 The key guiding principle of integrative
medicine is to use these interventions along with conventional pain management
approaches (eg, medications, radiation, injections, and physical therapies) and
it is not intended to replace conventional interventions.9

Patients often seek integrative medicine because they perceive that conventional
medical treatment is not completely meeting their needs, fear side effects from
pharmacotherapies, prefer a holistic approach, or because it has been
recommended by their family or health care providers.15-18 A growing number of
well-conducted randomized controlled trials (RCTs) have found that interventions
such as acupuncture or massage can alleviate pain in patients and survivors of
cancer.19-21 However, for many other interventions, trials are small and are
often limited by a lack of methodologic rigor. Ideally studies should not only
report the statistical significance of their findings but also the clinically
meaningful change in pain severity (a two-point reduction on a 0-10 scale).

To guide a patient-centered and evidence-based approach to pain management
incorporating integrative medicine interventions for appropriate
indications,9,22 clinicians and patients need to be equipped with knowledge of
the current evidence base of these therapies for pain management in cancer care.
The purpose of this guideline is to systematically appraise the evidence from
randomized controlled clinical trials, systematic reviews (SRs), and
meta-analyses, and to provide guidance to clinicians on the effectiveness of
integrative medicine treatment options for pain in adults and children with a
cancer diagnosis.

GUIDELINE QUESTIONS
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE QUESTIONS
<<METHODSRESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF INTER...DISCUSSIONPATIENT AND
CLINICIAN COM...HEALTH DISPARITIESGUIDELINE IMPLEMENTATION ...OPEN COMMENT
REVIEWLIMITATIONS OF THE RESEAR...FUTURE DIRECTIONSADDITIONAL
RESOURCESREFERENCES


This clinical practice guideline addresses two overarching clinical questions:
(1) What mind-body therapies are recommended for managing pain experienced by
adult and pediatric patients diagnosed with cancer? (2) What natural products
are recommended for managing pain experienced by adult and pediatric patients
diagnosed with cancer?

METHODS
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE QUESTIONSMETHODS
<<RESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF INTER...DISCUSSIONPATIENT AND
CLINICIAN COM...HEALTH DISPARITIESGUIDELINE IMPLEMENTATION ...OPEN COMMENT
REVIEWLIMITATIONS OF THE RESEAR...FUTURE DIRECTIONSADDITIONAL
RESOURCESREFERENCES

Guideline Development Process

Both the Society for Integrative Oncology (SIO) and ASCO regularly engage in the
development and dissemination of clinical practice guidelines. SIO's mission is
to advance evidence-based, comprehensive, integrative health care to improve the
lives of people affected by cancer. ASCO's mission is to conquer cancer through
research, education, and promotion of the highest-quality, equitable patient
care. For this guideline, SIO and ASCO joined efforts to develop a guideline
focused on the use of integrative therapies to manage oncology-related pain to
provide evidence-based recommendations to patients and clinicians to inform
clinical decisions. This guideline builds upon the existing ASCO guidelines on
pain management, the growing body of research in this area, and the emphasis
from the Centers for Disease Control and Prevention to use nonpharmacologic
approaches for pain management.2,23,24

This SR-based guideline product was developed by an international
multidisciplinary Expert Panel, which included a patient representative and a
health research methodologist (Appendix Table A2, online only). The Expert Panel
met via video conferences and corresponded through e-mail. Based upon the
consideration of the evidence, the authors were asked to contribute to the
development of the guideline, provide critical review, and finalize the
guideline recommendations. The guideline recommendations were sent for an open
comment period of two weeks allowing the public to review and comment on the
recommendations after submitting a confidentiality agreement. These comments
were taken into consideration while finalizing the recommendations. Members of
the Expert Panel were responsible for reviewing and approving the penultimate
version of the guideline, which was then submitted to the Journal of Clinical
Oncology (JCO) for editorial review and consideration for publication. All
SIO-ASCO guidelines are ultimately reviewed and approved by the Expert Panel,
the SIO Clinical Practice Guidelines Committee, and the ASCO Evidence Based
Medicine Committee before publication. All funding for the administration of the
project was provided by SIO.

The recommendations were developed by using a SR of evidence identified through
online searches of PubMed (1990-2021) and Cochrane Library (1990-2021) of RCTs,
SRs, and meta-analyses. Articles were selected for inclusion in the SR on the
basis of the following criteria:

 * Population: Adults and pediatric patients experiencing pain during any stage
   of their cancer care trajectory

 * Interventions: Integrative interventions for pain management, including
   acupuncture, acupressure, mind-body therapies, and natural products (note:
   see details in the Data Supplement, online only; therapies focused on pain
   prevention were not included)

 * Comparisons: No intervention, waitlist, usual care (UC) or standard care,
   guideline-based care, active control, attention control, placebo, or sham
   interventions

 * Outcomes: Pain intensity, reduction, or change in symptoms reported as the
   primary outcome in published manuscript

 * Sample size: Minimum total sample size of 20



Articles were excluded from the SR if they were (1) meeting abstracts not
subsequently published in peer-reviewed journals; (2) editorials, commentaries,
letters, news articles, case reports, and narrative reviews; or (3) published in
a non-English language. The guideline recommendations were crafted, in part,
using the Guidelines Into Decision Support methodology and the accompanying
BRIDGE-Wiz software program.25 In addition, a guideline implementability review
was conducted. On the basis of the implementability review, revisions were made
to the draft to clarify recommended actions for clinical practice. Ratings for
type and strength of the recommendation, and evidence quality are provided with
each recommendation. The quality of the evidence for each outcome was assessed
using the Cochrane Risk-of-Bias tool26 by the project methodologist in
collaboration with the Expert Panel cochairs and reviewed by the full Expert
Panel.

The SIO and ASCO Expert Panel and guidelines staff will work with cochairs to
keep abreast of any substantive updates to the guideline. On the basis of formal
review of the emerging literature, SIO will determine the need to update the
guideline. The SIO Guidelines Methodology Manual (available at
https://integrativeonc.org/practice-guidelines/sio-guidelines-guidelines-methodology)
provides additional information about the guideline process.

Guideline Disclaimer

The Clinical Practice Guidelines and other guidance published herein are
provided by the SIO and the ASCO to assist health care providers in clinical
decision making. The information herein should not be relied upon as being
complete or accurate, nor should it be considered as inclusive of all proper
treatments or methods of care or as a statement of the standard of care. With
the rapid development of scientific knowledge, new evidence may emerge between
the time information is developed and when it is published or read. The
information is not continually updated and may not reflect the most recent
evidence. The information addresses only the topics specifically identified
therein and is not applicable to other interventions, diseases, or stages of
diseases. This information does not mandate any particular course of medical
care. Further, the information is not intended to substitute for the independent
professional judgment of the treating clinician, as the information does not
account for individual variation among patients. Recommendations specify the
level of confidence that the recommendation reflects on the net effect of a
given course of action. The use of words like “must,” “must not,” “should,” and
“should not” indicate that a course of action is recommended or not recommended
for either most or many patients, but there is latitude for the treating
clinician to select other courses of action in individual cases. In all cases,
the selected course of action should be considered by the treating clinician in
the context of treating the individual patient. Use of the information is
voluntary.

SIO and ASCO do not endorse third-party drugs, devices, services, therapies,
apps, or programs used to diagnose, treat, monitor, manage, or alleviate health
conditions. Any use of a brand or trade name is for identification purposes
only. SIO and ASCO provide this information on an “as is” basis and make no
warranty, express or implied, regarding the information. SIO and ASCO
specifically disclaim any warranties of merchantability or fitness for a
particular use or purpose. SIO and ASCO assume no responsibility for any injury
or damage to persons or property arising out of or related to any use of this
information, or for any errors or omissions.

Guideline and Conflicts of Interest

The Expert Panel was assembled in accordance with SIO's and ASCO's shared
Conflict of Interest Policy Implementation for Clinical Practice Guidelines
(“Policy,” found at
https://integrativeonc.org/practice-guidelines/guidelines-sops and
https://www.asco.org/guideline-methodology). All members of the Expert Panel
completed SIO's disclosure form, which requires disclosure of financial and
other interests, including relationships with commercial entities that are
reasonably likely to experience direct regulatory or commercial impact as a
result of promulgation of the guideline. Categories for disclosure include
employment; leadership; stock or other ownership; honoraria, consulting, or
advisory role; speaker's bureau; research funding; patents, royalties, other
intellectual property; expert testimony; travel, accommodations, expenses; and
other relationships. In accordance with the Policy, the majority of Expert Panel
did not disclose any relationships constituting a conflict under the Policy.

RESULTS
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE QUESTIONSMETHODSRESULTS
<<RECOMMENDATIONSEVIDENCE SUMMARY OF INTER...DISCUSSIONPATIENT AND CLINICIAN
COM...HEALTH DISPARITIESGUIDELINE IMPLEMENTATION ...OPEN COMMENT
REVIEWLIMITATIONS OF THE RESEAR...FUTURE DIRECTIONSADDITIONAL
RESOURCESREFERENCES

Characteristics of Studies Identified in the Literature Search

A total of 1,346 articles were identified in the literature search. After
applying the eligibility criteria, 227 articles remained, forming the
evidentiary basis for the guideline recommendations.

TABLE 1. Studies on Interventions With Sufficient Evidence to Inform
Recommendations


View larger version (302K)



The identified trials were published between 1990 and 2021. The trials compared
various integrative therapies to standard of care, placebos, sham interventions,
other interventions, or active controls. The primary outcome for most of the
studies included pain severity, pain reduction, and change in pain symptoms,
which were measured with commonly used standardized tools such as the Visual
Analog Scale (VAS), Brief Pain Inventory scale (BPI), Numerical Rating Scale
(NRS), etc. Characteristics of the included studies are in the Data Supplement,
and Figure 1 presents the Preferred Reporting Items for Systematic Reviews and
Meta-Analyses flow diagram for the SR. Table 1 includes a breakdown of the
included studies by integrative therapies and pain indication, and Table 2
includes studies on interventions with insufficient or inconclusive evidence to
inform recommendations.

FIG 1. Systematic review flow diagram. RCT, randomized controlled trial; SR,
systematic review.



TABLE 2. Studies on Interventions With Insufficient or Inconclusive Evidence to
Inform Recommendations


View larger version (651K)


Study Quality Assessment

Study design aspects related to individual study quality, quality of evidence,
strength of recommendations, and risk of bias were assessed for the 227
intervention studies identified. SRs and meta-analyses were assessed for quality
using the assessment of multiple systematic reviews (AMSTAR) tool.252 Design
elements, such as blinding, allocation concealment, sufficient sample size,
intention-to-treat, and funding sources, were assessed for RCTs using the
Cochrane Risk-of-Bias tool.26 Overall, the included SRs were conducted using
established methods; however, many of the primary studies included in these
reviews suffered from flaws and/or limitations in study design. Ultimately, we
used the SRs as one of the means to identify relevant primary studies.
Additional RCTs identified and included in this guideline ranged from low to
high overall risk of bias in one or more key domains. Some of the flaws in the
study design included lack of blinding; incomparable control arms, small sample
sizes and/or high attrition rates; and limited statistical power, all of which
lowered the confidence in the findings. The included studies were also
heterogeneous with respect to patient populations, sample size, methodologic
quality, treatment duration, and outcome measures. The primary outcomes varied
across studies and, in most cases, were not directly comparable because of
different outcomes, measurements, and instruments used at different time points.
This diversity precluded a quantitative analysis and, as such, only a
descriptive review was performed. Refer to the Data Supplement for quality
rating scores and the Methodology Manual for more information and for
definitions of ratings for overall potential risk of bias.

RECOMMENDATIONS
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE
QUESTIONSMETHODSRESULTSRECOMMENDATIONS <<EVIDENCE SUMMARY OF
INTER...DISCUSSIONPATIENT AND CLINICIAN COM...HEALTH DISPARITIESGUIDELINE
IMPLEMENTATION ...OPEN COMMENT REVIEWLIMITATIONS OF THE RESEAR...FUTURE
DIRECTIONSADDITIONAL RESOURCESREFERENCES

Aromatase Inhibitor–Related Joint Pain
Recommendation 1.1.

Acupuncture should be offered to patients experiencing AI-related joint pain in
breast cancer (Type: Evidence based, benefits outweigh harms; Evidence quality:
Intermediate; Strength of recommendation: Moderate).

Literature review.

Four SRs and five RCTs were conducted in the area of acupuncture and AI-related
joint and muscle pain.19,27-30,44-47 The most definitive evidence is from a
phase III sham-controlled RCT conducted among 226 patients with moderate to
severe AI-related joint pain.19 After 6 weeks, true acupuncture reduced pain
significantly more than sham acupuncture and standard of care (waitlist control;
2.05, 1.07, and 0.99 points, respectively, on a 0-10 point NRS). After 6 weeks,
there were more responders who had a clinically meaningful change in pain (a
two-point reduction on a 0-10 scale)253 in the true acupuncture group compared
with the sham and waitlist control groups (58%, 33%, and 31% respectively).

Recommendation 1.2.

Yoga may be offered to patients experiencing AI-related joint pain in breast
cancer (Type: Evidence based, benefits outweigh harms; Evidence quality: Low;
Strength of recommendation: Weak).

Literature review.

In one RCT (N = 142),254 a 4-week yoga intervention was compared with a waitlist
control among breast cancer survivors currently receiving hormone therapy
(including AIs or tamoxifen) and who reported moderate to severe pain, muscle
aches, and body aches (> 2 on 0-4 scale) at baseline. Compared with women
randomly assigned to wait-list control, a significantly greater proportion of
women randomly assigned to yoga had reductions in total body aches (yoga 88.0% v
control 56.7%; P = .02), while there was a trend for pain (yoga 57.1% v control
37.1%; P = .09). Limitations of this trial include the analysis of pain as a
secondary outcome as the parent trial was powered for insomnia.254

Clinical interpretation.

Since AI-related joint pain affects up to 50% of women on this class of drugs
and negatively affects quality of life and adherence to hormonal treatment, we
recommend that acupuncture should be used for management of this painful
condition. Our recommendation is based on the available evidence for managing
this challenging condition and clinical importance of this issue. Many studies
showed joint pain results in nonadherence to AIs7,8 and such behavior can lead
to increased recurrence and mortality for women with breast cancer.255 Funding
to study nonpharmacologic approaches to pain and symptom management is highly
limited partly because of the lack of industry support. To date, only
acupuncture, duloxetine,256 and supervised exercise257 have been found to
improve AI-induced pain in large RCTs258 but only one large definitive trial for
each intervention has been conducted. Despite the recommendation, the decision
to use acupuncture with other treatments for AI-related pain needs to be based
on patient preference, benefit versus risk for each therapy, and availability of
and access to the treatment modality. Yoga, other mind-body therapies, and
natural products require additional well-conducted RCTs to increase the quality
of evidence to inform a change in the level of recommendation, if warranted.

General Cancer Pain or Musculoskeletal Pain
Recommendation 1.3.

Acupuncture may be offered to patients experiencing general pain or
musculoskeletal pain from cancer (Type: Evidence based, benefits outweigh harms;
Evidence quality: Intermediate; Strength of recommendation: Moderate).

Literature review.

Eight RCTs investigated the effect of acupuncture on general cancer pain or
general musculoskeletal pain among patients with cancer.20,48-54 Among them,
only one RCT had a large sample size,20 with 360 patients allocated in a 2:1:1
ratio into electroacupuncture (EA), auricular acupuncture (AA), and UC. It
showed that EA reduced pain by 1.9 points on a 0-10 NRS, and AA reduced pain by
1.6 points compared with UC at the end of treatment. In addition, the treatment
effects were durable at six months from random assignment. Both EA and AA were
associated with minimal toxicities, although more patients withdrew early from
the AA group because of ear pain.20 Given the large sample size and large effect
size, although there was no blinded sham control, the committee determined that
patients may consider using acupuncture to manage chronic musculoskeletal pain.

Recommendation 1.4.

Reflexology or acupressure may be offered to patients experiencing pain during
systemic therapy for cancer treatment (Type: Evidence based, benefits outweigh
harms; Evidence quality: Intermediate; Strength of recommendation: Moderate).

Literature review.

There were seven randomized trials, evaluating the effectiveness of reflexology
to reduce pain during systemic therapy (chemotherapy, chemoradiotherapy,
targeted, and/or hormonal therapy) with six trials showing significantly less
pain in the intervention group compared with the controls.92-96,98 These studies
included patients with different cancer types and used different methods to
implement the reflexology intervention that was provided (provided by a
reflexologist,92,93,95-97 administered by a trained caregiver94,98). Four trials
included fewer than 50 patients per arm, but three trials included more than 90
patients per arm.94,97,98 The type of control varied between trials (attention
control,94,98 usual or standard care,95-97 and other active treatment such as
relaxation) and two trials94,97 blinded patients to the group assignments.

Recommendation 1.5.

Massage may be offered to patients experiencing chronic pain following breast
cancer treatment (Type: Evidence based, benefits outweigh harms; Evidence
quality: Low; Strength of recommendation: Moderate).

Literature review.

In a SR and meta-analysis,101 five randomized trials with a total of 127
patients with chronic musculoskeletal pain after breast cancer treatment were
included. Three studies were of high methodologic quality and in one study,
patients were blinded for the intervention. The trial interventions included
myofascial induction, myofascial release, classic massage, ischemic compression
of trigger points, and myofascial therapy. Controls used in the trials included
an educational session, physical therapy, or sham control. In the massage
therapy group, the pain was decreased by a small to moderate effect size
(standardized mean difference [SMD] 0.32) compared with the controls. On the
basis of the available data, massage may be offered to decrease pain intensity
in women who have completed surgical treatment, chemotherapy, and/or radiation
therapy for breast cancer.

Recommendation 1.6.

Hatha yoga may be offered to patients experiencing pain after treatment for
breast or head and neck cancers (Type: Evidence based, benefits outweigh harms;
Evidence quality: Low; Strength of recommendation: Weak).

Literature review.

Two RCTs evaluated hatha yoga for musculoskeletal pain among patients'
postcancer treatment: One RCT for musculoskeletal pain associated with head and
neck cancer76 (N = 40) and the second evaluated hatha yoga for musculoskeletal
pain among patients with breast cancer (N = 42).77 Both trials had small sample
sizes, and follow-up assessments were completed at similar intervals (8 weeks,
2.5 months). In one trial, statistically significant differences were observed
among patients with head and neck cancer on the BPI (short form), including in
patterns of change in pain (P < .001, SMD = 0.90), and pain interference with
activities of daily living (BPI Interference, P = .005, SMD = 0.67). In the
second trial among patients with breast cancer, the yoga group demonstrated
significant improvement in shoulder and arm pain severity from baseline to
post-treatment (P = .01 and P = .01, respectively). Pain reduction was
maintained at 2.5 months post-treatment (P = .01 and P = .01, respectively).
However, the control group demonstrated no significant difference between
pretreatment and post-treatment pain levels. These findings provide preliminary
evidence supporting the efficacy of hatha yoga for pain after head and neck or
breast cancer treatment, although given the small sample sizes and lack of
attention controls, the quality of the evidence is low.

Recommendation 1.7.

Guided imagery with progressive muscle relaxation (PMR) may be offered to
patients experiencing general pain from cancer treatment (Type: Evidence based,
benefits and harms not assessable; Evidence quality: Low; Strength of
recommendation: Weak).

Literature review.

Four RCTs were identified for evaluation of guided imagery and PMR for patients
experiencing pain because of a cancer diagnosis.80,81,125,126 These studies
included multiple types of cancers, and two of these studies included
intervention arms that included only 20 participants.81,125 One included an
intervention arm of approximately 100 participants.126 The largest and one of
the smaller studies reported decreased pain levels with the intervention
compared with the control. One of the studies used audio recorded instruction of
PMR and mental imagery as well as live instruction and a control group. Blinding
of participants, health professionals, data collectors, and data analysts was
inconsistent. These factors adversely affected study quality overall. With only
some favorable findings, overall lack of safety data, and quality concerns,
guided imagery and PMR may be offered to patients experiencing cancer-related
pain, but the strength of the recommendation is weak.

Clinical interpretation.

General cancer pain and musculoskeletal pain are common among patients with
cancer and can persist even years after cancer treatment. Management of pain
requires an interdisciplinary approach that includes pharmacologic treatments
(both nonopioid and opioid drugs depending on the severity), physical therapy,
and psychotherapy. There is moderate evidence that acupuncture can be used to
manage general cancer pain or chronic musculoskeletal pain. In addition,
reflexology can be incorporated into systemic cancer treatment. The other
integrative medicine interventions, despite some demonstrating promising
preliminary results, have low level of evidence because of limited research and
methodologic challenges; therefore, more rigorous research is needed.

Chemotherapy-induced Peripheral Neuropathy
Recommendation 1.8.

Acupuncture may be offered to patients experiencing CIPN from cancer treatment
(Type: Evidence based-informal consensus, benefits outweigh harms; Evidence
quality: Low; Strength of recommendation: Weak).

Literature review.

There were two SRs31,32 and seven RCTs56-62 with small sample sizes
investigating the effect of acupuncture on CIPN. No major toxicities were
reported in any studies, and most studies showed a benefit of acupuncture for
CIPN pain. In a phase II trial (N = 75), acupuncture was associated with
significant reduction in CIPN pain, whereas sham acupuncture and UC were not
(1.75, 0.91, and 0.19 points, respectively, on a 0-10-point NRS). However, the
small sample sizes and high or unclear risk of biases in the studies resulted in
low level of evidence.62

Recommendation 1.9.

Reflexology or acupressure may be offered to patients experiencing CIPN from
cancer treatment (Type: Evidence based, benefits outweigh harms; Evidence
quality: Low; Strength of recommendation: Weak).

Literature review.

Two small RCTs with approximately 30 patients per arm evaluated the
effectiveness of reflexology for reducing CIPN symptoms, including pain,
compared with the control.99,100 One trial in patients with multiple cancers
compared the effects of reflexology foot massage twice a day for 20 minutes over
6 weeks to standard hospital care.99 This study found improvement in sensory
functions in the reflexology group compared with the control group but no group
differences for peripheral neuropathy-related pain severity and incidence. The
second study was in patients with gynecologic cancers and tested a self-care
reflexology approach.100 Patients in the intervention group were trained to
perform aromatherapy self-foot reflexology (three times a week, for 15 minutes
on each foot, 18 sessions over a period of 6 weeks) and were compared with a
waitlist control. The intervention group showed lower levels of peripheral
neuropathy symptoms, less interference with daily activities, and higher
peripheral skin temperature level. In addition, the self-foot massage seemed to
have had a positive effect on mood symptoms. Furthermore, side effects were not
reported in either study or, therefore, the potential benefits likely outweigh
the potential harms.

Clinical interpretation.

CIPN is a highly common, persistent, and debilitating toxicity that not only
negatively decreases quality of life but also increases risk for falls.259
Duloxetine provides modest effect for CIPN pain,23 but it has side effects
poorly tolerated by some patients. On the basis of preliminary efficacy and
favorable risk-benefit ratio, acupuncture may be recommended. A phase III
acupuncture for CIPN trial is ongoing and will help more definitively clarify
the role of acupuncture for this debilitating painful condition
(ClinicalTrials.gov identifier: NCT04917796). In addition, albeit with low
levels of evidence, aromatherapy self-foot-reflexology may be considered part of
self-care for some patients for CIPN pain to improve patients' self-efficacy and
to empower them to be more active participants during their cancer care; larger
trials would be needed for evidence-based recommendations.

Surgical or Procedural Pain
Recommendation 1.10.

Hypnosis may be offered to patients experiencing pain during cancer treatment
procedures or diagnostic workups (Type: Evidence based, benefits outweigh harms;
Evidence quality: Intermediate; Strength of recommendation: Moderate).

Literature review.

Five studies have evaluated the use of hypnosis during procedures,87-91
including three with methodologic weaknesses and two well-designed studies with
an attention control as well as a standard-of-care arm.88,91 The two most
rigorous trials with more than 200 randomly assigned participants each evaluated
hypnosis for large core breast biopsies91 and tumor embolization or
radiofrequency ablation.88 Both studies demonstrated significantly lower pain
ratings compared with control arms with a median reduction of ≥ 2 (0-10 point
scale) reported during the procedure. On the basis of these two trials, hypnosis
may be recommended to help manage pain during procedures. Importantly, both
studies involved hypnosis provided throughout the procedure, not just for a
short time before the procedure.

Clinical interpretation.

Procedures such as biopsy or tumor embolization play an important role in
diagnosis and treatment of cancer. However, they are associated with acute pain
and frequently require management with intravenous or oral pain medications that
have a few side effects. There is moderate evidence for self-hypnosis to be
taught and used to prevent treatment procedure-related pain. However, for the
other interventions such as mindfulness-based interventions, music therapy, and
virtual reality–based imagery interventions, despite their appeal and potential
effect, research is very much needed to establish a robust evidence base.

Recommendation 1.11.

Acupuncture or acupressure may be offered to patients undergoing cancer surgery
or other cancer-related procedures such as bone marrow biopsy (Type: Evidence
based-informal consensus, benefits outweigh harms; Evidence quality: Low;
Strength of recommendation: Weak).

Literature review.

There were 12 RCTs assessing the effect of acupuncture or acupressure in
reducing pain associated with surgery or procedure.64-75 They are all limited by
small sample sizes and an unclear or high risk of bias. Among them, two involved
acupressure for bone marrow aspiration and biopsy pain,64,65 one was on
acupuncture and mastectomy pain,66 and nine were on postoperative pain.67-75 The
two acupressure and bone marrow aspiration and biopsy pain RCTs showed that
acupressure significantly reduced the proportion of patients who experienced
severe pain than sham acupressure (2.7% v 20%, P = .03),64 and acupressure
resulted in the lowest procedural pain score when compared with sham acupressure
or sham (P = .001).65 A trial of acupuncture for mastectomy pain (N = 30) showed
that acupuncture significantly reduce pain, nausea, and anxiety in the first 2
postoperative pain days when compared with UC.66 Among the nine RCTs on
acupuncture versus control groups to reduce postoperative pain, six trials
showed no statistical difference between the two groups, and three showed
acupuncture treatment resulted in lower pain score.68-70 Adequately powered and
well-designed trials are needed to establish the definitive efficacy of
acupuncture. Although the quality of evidence was deemed low, the benefit seems
to outweigh the risk; therefore, the panel determined that patients may explore
use of acupuncture or acupressure to reduce surgical and procedure-related pain.

Recommendation 1.12.

Music therapy may be offered to patients experiencing surgical pain from cancer
surgery (Type: Evidence based, benefits outweigh harms; Evidence quality: Low;
Strength of recommendation: Weak).

Literature review.

Although all the three studies in this section demonstrated a significant effect
of music therapy to improve surgical pain scores more than UC, quality of
evidence is low as two trials showed high risk of bias117,118 and one was a
small study to test the hypothesis.116 A trial of 60 patients undergoing lung
cancer resection indicated potential association between music therapy and the
need for less analgesic medication, including opioid drugs.118 The smallest
study of 30 mastectomy patients used a high-dose (4 hours of recorded music)
music therapy intervention and found the music therapy group experienced a 41.4%
less increase in pain from time 1 (preoperative) to time 2 (postoperative)
compared with women in the control.116 Similarly, a trial of 120 women with
breast cancer undergoing radical mastectomy surgery in China found a
statistically significant improvement in the primary end point (change in Pain
Rating Index scores from baseline [the first day after radical mastectomy
(pretest)]) for the music therapy group compared with the control group (–2.38
(95% CI, –2.80 to –1.95), P < .001) at the first post-test (evaluation on the
day before discharge from hospital). This improvement remained significant,
although the difference narrowed, at the third post-test (evaluation on the day
of admission for second chemotherapy session).

Clinical interpretation.

Cancer surgery is associated with acute pain and can also lead to chronic pain.
The primary mode of pain management during the perioperative or postoperative
periods involves anesthesia, opioid, and nonopioid drugs. Despite the
preliminary evidence and potential value of several integrative medicine
interventions such as acupuncture, music therapy, or massage, the quality of
research evidence is low and insufficient. Adequately powered clinical trials
evaluating the effectiveness of these interventions in the perioperative or
postoperative settings are needed to guide further recommendations.

Pain During Palliative Care
Recommendation 1.13.

Massage may be offered to patients experiencing pain during palliative and
hospice care (Type: Evidence based, benefits outweigh harms; Evidence quality:
Intermediate; Strength of recommendation: Moderate).

Literature review.

A SR from 2009 assessing 14 low-quality trials concluded (on the basis of four
trials) that there is encouraging evidence that massage can alleviate pain in
palliative cancer patients with various types of cancers.103 A more recent SR
from 2020 included three RCTs evaluating the effectiveness of massage for pain
in patients receiving palliative treatment, all of them showing favorable
results for massage.40 Although two studies included smaller samples (10-20
patients per arm), the third trial was a high-quality large multicenter trial21
that was also included in the previous SR. A total of 380 adults with various
types of advanced cancers who were experiencing moderate-to-severe pain were
included (90% were enrolled in hospice) and randomly assigned to massage or
simple touch sessions (six 30-minute sessions over 2 weeks). The intervention
included gentle gliding stroke; squeezing, rolling, and kneading the muscles;
and trigger point release, while the control group received simple touch.
Immediate outcomes were obtained just before and after each treatment session on
a 0- to 10-point scale (Memorial Pain Assessment Card), and sustained outcomes
(including BPI) were obtained at baseline and weekly for 2 weeks. Massage seems
to have an immediate beneficial effect on pain reduction (mean difference, 0.90;
P < .001), and no side effects were observed. No between-group mean differences
occurred over time in the sustained measurements of pain. On the basis of the
available favorable data from multiple trials, massage may be offered to
patients experiencing pain during palliative and hospice care.

Clinical interpretation.

Effective pain management is a central component in providing high-quality
palliative care. On the basis of moderate evidence, massage can be incorporated
into palliative and hospice setting to provide short-term pain relief and
enhance coping for patients living with advanced cancer. The research is very
limited in both quantity and quality for other interventions to make sound
recommendations for pain management in this population. Chronic pain management
in cancer survivorship is also essential for improving quality of life and
functional recovery. With the ongoing opioid epidemic in the United States,
Canada, and other countries, rigorous research and appropriate implementation
and integration of nonpharmacologic interventions (eg, acupuncture, yoga, and
massage) even as first-line pain management is needed for the growing population
of cancer survivors.

Figure 2 provides a visual representation of these recommendations in the
treatment algorithm. Table 3 shows the breakdown of the summary of
recommendations.

FIG 2. Treatment algorithm. CIPN, chemotherapy-induced peripheral neuropathy.



TABLE 3. Summary of Recommendations


View larger version (548K)


EVIDENCE SUMMARY OF INTERVENTIONS WITH INSUFFICIENT OR INCONCLUSIVE EVIDENCE TO
INFORM AN ACTIONABLE RECOMMENDATION
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE
QUESTIONSMETHODSRESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF INTER...
<<DISCUSSIONPATIENT AND CLINICIAN COM...HEALTH DISPARITIESGUIDELINE
IMPLEMENTATION ...OPEN COMMENT REVIEWLIMITATIONS OF THE RESEAR...FUTURE
DIRECTIONSADDITIONAL RESOURCESREFERENCES

Adult Population
Natural products for AI-related joint pain.

There is insufficient evidence to recommend for or against use of omega-3 fatty
acids, Yi Shen Jian Gu granules, or topical pure emu oil to manage AI-related
pain. Four trials tested the effects of natural products on the treatment of
AI-induced pain in patients with breast cancer. Two randomized,
placebo-controlled trials tested the effects of omega-3 fatty acids on the
prevention and treatment of AI-induced musculoskeletal pain.191,192 The first
trial was a large multisite trial that tested the effects of omega-3 fatty acids
on reducing AI-induced musculoskeletal pain in women with a history of breast
cancer (N = 262).192 In this trial, improvements were observed in both the
omega-3 fatty acid and placebo (soybean or corn oil) arms with no differences
between groups. The second trial was a smaller pilot and feasibility trial,
again testing the effects of omega-3 fatty acids on preventing AI-induced
arthralgias in patients with breast cancer (N = 44) and found no differences in
pain severity between groups.191 One trial tested the effects of a combination
of Chinese herbal formulation Yi Shen Jian Gu granules,203 while another tested
topical pure emu oil.204 The emu oil did not yield differences compared with the
placebo. However, the women who received Yi Shen Jian Gu (n = 40) appeared to
have improved pain at 12 and 24 weeks. Given that there was only one trial of
each treatment intervention with relatively small sample sizes, there are
insufficient data to make a clinical recommendation.

General cancer pain.
Music therapy.

There is insufficient evidence to recommend for or against the use of music
therapy for patients experiencing general cancer pain. Of the three studies
identified, only two trials specified pain as a primary outcome and were,
therefore, reviewed.114,115 These two trials did not contribute evidence of
music therapy as effective for generalized oncology pain because of methodologic
flaws. One RCT compared one-time 30-minute sedative music therapy, instrumental
intervention versus UC for 126 inpatient oncology patients experiencing levels
of pain rated three and greater on a 0-10 numerical rating scale.114 The music
therapy intervention included self-selected music styles intended for relaxation
or distraction. The other study compared music therapy (passive listening to
instrumental music) to poetry (listening to spoken-word poetry) in a three-arm
trial with the control group receiving usual inpatient care.115 Use of opioid
analgesics and nonsteroidal anti-inflammatory drugs were reported for both
groups, with no significant difference of use between groups. Primary outcomes
were changes in daily pain levels over the 3 days during which music or poetry
was offered. Both intervention groups showed statistically significant
improvements in perceptions of pain, which may indicate that it was the
distraction provided by the interventions that was sufficient to decrease
perception of pain, and not effects specific to music therapy.

Herbal products.

There is insufficient evidence to recommend for or against the use of Xiao Zheng
Zhitong paste, Jinlongshe granule, Shuangbai San paste, or Xiao-Ai-Tong
decoction for general cancer pain. Four trials tested the effects of Chinese
herbal preparations on treating general cancer pain, including Xiao Zheng
Zhitong paste in patients with a range of different cancer types,207 Jinlongshe
granules in patients with gastric cancer,208 Shuangbai San paste in patients
with liver cancer,209 and Xiao-Ai-Ton decoction with and without morphine in
patients with a range of different cancer types.206 Given that there was only
one trial of each treatment intervention, variability in quality of the trials,
there are insufficient data to make a clinical recommendation.

Chemotherapy-induced peripheral neuropathy.
Natural products.

There is insufficient evidence to recommend for or against the use of omega-3
fatty acids, and glutamine to patients experiencing CIPN from cancer treatment.
A single moderate-size randomized, double-blind, placebo-controlled trial (N =
69) tested the effects of omega-3 fatty acid on reducing the incidence and
severity of peripheral neuropathy in patients with breast cancer receiving
paclitaxel chemotherapy.194 Trial results showed that patients receiving the
omega-3 fatty acids were less likely to develop peripheral neuropathy, but there
were no differences in severity of neuropathy and motor nerve conduction
measurements. Although the trial results are intriguing, subsequent trials need
to replicate and confirm these findings before a clinical recommendation can be
made.

Two RCTs tested the effects of glutamine on the incidence and severity of
peripheral neuropathy.186,187 The first trial was a moderate-size (N = 86) trial
comparing oral levo-glutamine compared with no intervention in patients with
colorectal cancer receiving oxaliplatin.186 Patients who received levo-glutamine
had lower incidence and severity of peripheral neuropathy symptoms; however, the
trial did not control for placebo effects. The second smaller trial (N = 43)
compared oral glutamate to placebo in women with ovarian cancer receiving
paclitaxel.187 There were no differences between groups in incidence of
peripheral neuropathy; patients who received glutamate reported lower pain
severity. No clinical recommendations can be made on the basis of these results
because of low study quality and/or small sample size.

Surgical or procedural pain.
Meditation-based interventions.

There is inconclusive evidence to recommend for or against the use of
meditation-based interventions to patients with breast cancer experiencing
procedural pain. Four RCTs evaluated meditation or mindfulness-based
interventions for patients experiencing procedural pain for breast
cancers.127-130 Two studies examined loving-kindness meditation versus music
intervention versus UC, and showed loving-kindness meditation's superiority to
UC, but not to music.129,130 The third study examined guided meditation plus
massage versus massage alone, and showed no significant difference between study
arms.128 The fourth study was composed of three arms comparing guided
mindfulness-based meditation to guided focused breathing and standard of care in
women scheduled for stereotactic breast biopsy.127 The result of this study was
also negative. All four studies were relatively small in size (n < 50 per arm).
The mixed findings suggest that meditation-based therapies are not superior to
active control conditions, but it is likely that these studies were
underpowered. In the absence of fully powered trials, there are no clear
indications for meditation-based therapies for patients experiencing procedural
pain for breast cancers.

Music therapy.

There is inconclusive evidence to recommend for or against the use of music
therapy to patients experiencing procedural pain. The five trials
reviewed119-123 showed either no effect119,123 or suffered from various
methodologic flaws, including weak music therapy interventions,122 high risk of
bias in trial methodology,121 inadequate assessment and reporting of pain
scores,121,122 and inconsistent tracking of analgesic or anxiolytic medication
provided during the intervention period.120,121 These studies, therefore,
yielded results insufficient to determine the effect of music therapy on
procedural pain.

Reflexology.

There is insufficient evidence to recommend for or against the use of
reflexology for pain associated with surgery or procedure. There is only one
small, randomized trial138 (n = 31 patients per arm) in patients with gastric or
liver cancer who received major abdominal surgery evaluating the effectiveness
of foot reflexology compared with a control. The foot reflexology was provided
at least 24 hours after surgery by a trained reflexologist (10 minutes on each
foot for 3 consecutive days). The control group received routine care. The
results were inconclusive; although there was no significant group difference
for the McGill Pain Questionnaire, the VAS showed a difference in favor of the
intervention group. The present data are insufficient to recommend the use of
reflexology for pain associated with cancer-related surgery or procedures.

Hypnosis.

There is inconclusive evidence to recommend for or against the use of hypnosis
in treating surgical pain in patients with cancer. Two studies evaluated
hypnosis for surgical pain with inconsistent results.84,85 Montgomery et al85
randomly assigned 200 patients with breast cancer scheduled for excisional
biopsy or lumpectomy to 15-minute hypnosis intervention before surgery versus an
attention control. Subjects in the hypnosis group reported less pain intensity
(means = 22.43 v 47.83; difference = 25.40; 95% CI, 17.56 to 33.25) and pain
unpleasantness (means = 21.19 v 39.05; difference = 17.86; 95% CI, 9.92 to
25.80). Hypnosis also led to decreased utilization of propofol and lidocaine
compared with controls. The second study allocated 150 patients with breast
cancer scheduled for minor breast surgery to hypnosis (≤ 15 minutes) versus UC
control.84 The study found increased mean pain in the hypnosis arm (2.63,
standard deviation 1.62) versus control (1.75, standard deviation 1.59; P =
.004) on a pain VAS (0-10). Despite the large and well-designed clinical trials,
the inconsistent results make any conclusions impossible at this time.

Massage.

There is inconclusive evidence to recommend for or against the use of massage
for peri-postoperative pain from major surgical procedures in breast and
gynecologic cancer. There were two RCTs evaluating the effectiveness of massage
for pain reduction after major surgical procedures in patients with breast
cancer. A small trial with 19 patients per arm undergoing autologous tissue
reconstruction showed no extra benefits in the massage group compared with
controls.128 Another trial with 30 patients per arm undergoing lymph node
dissection evaluated the effectiveness of postsurgical arm massage provided by
the patient's significant other.139 The intervention group reported less pain in
the immediate postoperative period than the control group that received no
massage. A three-armed trial analyzed 35 women per arm with gynecologic cancers
and compared Swedish massage with vibration and UC as additional treatment to
postoperative pain medication.141 The interventions were applied for 3
consecutive days after surgery. Massage showed only minor effects on short-term
sensory and affective pain. On this basis, the data are inconclusive to
recommend massage for peri-postoperative pain following major surgical
procedures in patients with breast and gynecologic cancer.

There is also insufficient evidence to recommend for or against the use of
massage for pain from minor surgical procedures. There are very little data
evaluating the effectiveness of massage to improve pain from minor surgical
procedures. In a pilot trial with 2:1 random assignment, 40 patients received a
20-minute massage before and after the surgical placement of a vascular access
device (port) and 20 patients received attention control.140 No relevant
differences in postsurgical pain were observed between both groups. The
available data are insufficient to recommend massage for pain following minor
surgical procedures.

Pain from survivorship and palliative care.
Meditation-based interventions.

There is inconclusive evidence to recommend for or against the use of
meditation-based interventions to patients experiencing pain after treatment or
survivorship for breast cancers. Three RCTs evaluated meditation-based
interventions for patients experiencing pain after treatment or survivorship for
breast cancer or bone cancer.131-133 One study was relatively small (n < 50 per
arm),133 reporting superiority of Mindfulness-Based Stress Reduction (MBSR) plus
music therapy over a waitlist control for reducing pain intensity in
osteosarcoma. The other two studies were moderately large (n > 50 per
arm),131,132 with one study demonstrating the superiority of Mindfulness-Based
Cognitive Therapy over a waitlist control for reducing late post-treatment pain
intensity in women with breast cancer.132 By contrast, the other trial (the
largest meditation-based intervention trial evaluated in this review, N = 322)
showed no effect of MBSR over a waitlist control for chronic pain in breast
cancer survivors who completed treatment.131 The null effect in this trial may
be associated with low baseline pain or the high heterogeneity of the sample
(women had completed treatment between 2 weeks to 2 years before study
enrollment). Adverse events were not reported for all four studies. Given these
mixed findings, and the lack of safety data, there are no clear indications for
meditation-based intervention for patients experiencing pain following treatment
or survivorship for breast or bone cancers.

Hypnosis.

There is inconclusive evidence to recommend for or against the use of hypnosis
in treating pain in cancer survivors (active treatment and post-treatment
survivors). Studies of hypnosis during cancer survivorship were limited because
of significant methodologic issues. Two studies combined hypnosis with another
intervention—support group135 or cognitive behavioral therapy.134 These studies
generally reported positive benefits; however, interpretation is limited because
of the combination approach. A study randomly assigned patients receiving a bone
marrow transplant to hypnosis training, cognitive behavioral coping, therapist
contact, and UC.136 The patients in the hypnosis arm attended two prehospital
sessions and then received taped recordings for daily practice while in the
hospital. Descriptive results showed lower oral pain in the hypnosis group but
were limited by the small numbers in each group (10-12 in each arm). Therefore,
this area could benefit from more research with large sample sizes.

Music therapy.

There is insufficient evidence to recommend for or against the use of music
therapy in treating palliative or chronic pain in patients with cancer. There
was only one study reviewed for music therapy for pain in patients receiving
palliative care.124 This trial was conducted as an RCT, but the group designated
as control received an effective intervention (MBSR involving deep breathing,
visual imagery, and muscle relaxation). Although the study was well designed and
blinded, pain scores did not change significantly and both groups improved in
relaxation and well-being scores. The dose for the music therapy intervention
was low, consisting of the availability of 45 minutes of prerecorded music on a
cassette tape player, which most participants in the music therapy group
reported listening to only 2-4 times per week. The music therapist met once with
each intervention group participant to choose the type of music they preferred.
The study, therefore, does not support the use of this music therapy
intervention for pain during palliative care.

Virtual reality.

There is insufficient evidence to recommend for or against the use of virtual
reality imagery and relaxation in treating palliative or chronic pain in
patients with cancer. Only two studies were identified for the use of virtual
reality imagery and relaxation interventions in adults, both for pain during
palliative care.142,143 The first study investigated female patients with breast
cancer experiencing pain and receiving analgesic painkillers (intravenous or
oral) in a palliative care setting.142 This trial did not specify the primary
outcome, and although both pain and anxiety were assessed, conclusions were that
an immersive virtual reality imagery and relaxation intervention is acceptable
in an Arab culture (study is from Jordan), and that virtual reality holds
promise as an effective distraction intervention for managing pain and anxiety
among this study population.142 The second trial also only studied female
patients with breast cancer who had undergone breast cancer surgery.143 Both
intervention and control groups received upper-extremity physiotherapy, with the
intervention group adding an Xbox 360 Kinect technology-based gamification of
physiotherapy for weeks 2 through 5 in addition to some additional physiotherapy
exercises. Both groups experienced statistically significant improvement over
time with no differences between groups.

Pain during radiation therapy and/or oral mucositis.
Hypnosis.

There is inconclusive evidence to recommend for or against the use of hypnosis
in treating radiotherapy-induced pain in patients with cancer. For radiotherapy,
only one study has been published.137 This study randomly assigned 68 patients
with head and neck cancer receiving radiotherapy to a single 20-minute session
of hypnosis or UC. The hypnosis treatment demonstrated significantly lower pain
scores –1.966 (95% CI, –2.260 to –1.673; P < .001) compared with controls. This
study should be considered hypothesis-generating.

Honey.

There is inconclusive evidence to recommend for or against the clinical use of
honey for oral mucositis. Nineteen trials tested the effects of honey on the
prevention and/or treatment of oral mucositis.148-166 The results across trials
are inconsistent and, thus, it is not possible to make a conclusive
recommendation. Study populations included patients with head and neck cancer
receiving radiation (some of whom also received chemotherapy),149-159,165
patients with acute myeloid leukemia receiving chemotherapy,160 patients with
chemotherapy-induced oral mucositis,163 patients with radiation therapy-induced
oral mucositis,164 and patients with lung cancer receiving chemotherapy and
radiation therapy.166 No two trials used the same honey preparation, dose, mode,
and/or timing of delivery. Some studies did suggest that the studied honey
preparation did provide some benefit, although the size and quality of the
studies limit the ability to draw definitive conclusions. The largest and most
rigorously designed trial was a three-arm trial conducted within the National
Clinical Trials Network NRG Oncology clinical trial network that tested the
effects of standard supportive care, liquid manuka honey, and manuka honey
lozenges in preventing radiation esophagitis in patients with lung cancer.
Neither honey arm was superior to supportive care in preventing radiation
esophagitis; however, the honey preparation in this trial was irradiated, which
may have inhibited the beneficial effect of bacteria within the honey. Because
of the heterogeneity of interventions and outcomes, the data are inconclusive on
the use of honey to prevent or treat oral mucositis.

Other natural products.

There is insufficient evidence to recommend for or against the clinical use of
chamomile, propolis, glutamine, curcumin, teas, mouthwashes, and other herbal
combinations. Multiple trials tested a variety of botanical and natural products
to prevent and/or treat mucositis in a range of different cancer types receiving
different chemotherapy and/or radiation therapy
treatments.167-174,188,189,195-202,211-229 Interventions included
chamomile,167,168 propolis,169-171 glutamine,172-185 curcumin,188-190 botanical
teas,195,196 mouthwashes,197-202 and other natural products (Data
Supplement).211-229 No two trials used the same formulation. Although some
trials suggested that there might be some benefit, most trials did not have
clearly defined end points and were not clearly powered to detect differences.
Thus, there are insufficient data to make clinical recommendations on the use of
these natural products for the prevention and/or treatment of oral mucositis.

Oral mucositis pain represents a challenging toxicity associated with radiation
and some chemotherapy agents. The current management often involves topical
local anesthetics, opioids, and liquid diets, and in many cases, patients
require a gastric tube for adequate nutrition. Despite tremendous unmet needs,
the research evidence for integrative medicine (both mind-body and natural
products) is low and requires thoughtful investigation to make evidence-informed
recommendations.

Pediatric Population

Although we sought out to evaluate the evidence of integrative medicine for pain
in pediatric population, there were very few trials in this population. Several
small RCTs focused on procedural pain: hypnosis,240-243 music therapy,245 and
virtual reality246,247 were conducted. Despite showing acceptability,
feasibility, and promising effect in some trials, these studies had substantial
methodologic flaws such as lack of appropriate control groups and small sample
size; therefore, there is insufficient evidence to support the use of hypnosis,
music therapy, and virtual reality in treating procedural pain in pediatric
patients with cancer. A number of RCTs evaluated various natural products for
oral mucositis pain with honey.148,161,162 The study populations included
pediatric patients receiving methotrexate,162 and other children receiving
chemotherapy and/or radiation therapy.148,161 The results from these studies
were inconsistent. Natural products (eg, vitamin E, Traumeel S, pine bark
extract, andiroba gel, and propolis) were evaluated in clinical trials as
treatment of chemotherapy-induced oral mucositis in children with
cancer226,248-251; however, these trials were early phase and had limited sample
size and poor control groups; therefore, the risk of bias was high; the evidence
for these therapies were insufficient or inconclusive.

Pain in children or infants with cancer is common during medical or surgical
treatment; however, because of the limited research in this area, no
recommendations can be made to incorporate integrative medicine intervention for
pain management. Research in alleviating pediatric pain and other symptoms is
particularly challenging because of the difficulty in assessing and measuring
children's pain, the involvement of parents, which adds complexity, and small
sample sizes. However, to provide evidence-informed integrative treatment for
children with cancer, novel research methods, carefully developed interventions,
and rigorous study design and conduct are needed for children with cancer and
their parents.

DISCUSSION
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE
QUESTIONSMETHODSRESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF INTER...DISCUSSION
<<PATIENT AND CLINICIAN COM...HEALTH DISPARITIESGUIDELINE IMPLEMENTATION ...OPEN
COMMENT REVIEWLIMITATIONS OF THE RESEAR...FUTURE DIRECTIONSADDITIONAL
RESOURCESREFERENCES


Pain remains a challenging clinical issue for both patients with cancer and
health care providers. Effective pain management requires careful consideration
of the research evidence for both pharmacologic and nonpharmacologic
interventions. On the basis of reviewing 198 RCTs and 26 SRs and meta-analyses,
several integrative medicine interventions can be considered for management of
pain in oncology settings, using rigorous criteria for the basis of
recommendations. Acupuncture should be recommended to manage AI-related joint
pain. Acupuncture and reflexology or acupressure may be recommended for general
cancer pain and musculoskeletal pain. Hypnosis may be recommended for patients
undergoing painful procedures, and massage may be recommended for patients
receiving palliative or hospice care. These recommendations were based on at
least intermediate quality of evidence and overall appraisal of benefits
outweighing potential harms. The use of other integrative medicine interventions
for other types of pain currently has low quality of evidence. This guideline
provides the evidence base for integrating selected integrative medicine
approaches into a comprehensive pain management strategy to improve symptom
control and quality of life for patients with cancer and survivors. In addition,
the review highlights the gaps in evidence that should inspire future research.

PATIENT AND CLINICIAN COMMUNICATION
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE
QUESTIONSMETHODSRESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF
INTER...DISCUSSIONPATIENT AND CLINICIAN COM... <<HEALTH DISPARITIESGUIDELINE
IMPLEMENTATION ...OPEN COMMENT REVIEWLIMITATIONS OF THE RESEAR...FUTURE
DIRECTIONSADDITIONAL RESOURCESREFERENCES


Effective communication between health care providers and their patients is
essential for patient-centered pain management. It is well documented that
physicians rarely inquire about the use of integrative medicine, and patients
often do not disclose such use.260 Health care providers need to have a
knowledge base to engage in meaningful communication with their patients about
integrative medicine use and provide answers to their questions.261 The results
of a large survey suggest that lack of knowledge about integrative medicine is
often the biggest barrier to use by patients, particularly among racial and
ethnic minorities and among those with less education.262,263 Patients with
positive beliefs about natural health approaches, higher treatment expectancy,
lower barriers, and with family endorsement are likely to prefer integrative
medicine over pharmacology to manage pain.17,263 Facilitating open communication
and acknowledging patient values and preferences will enable shared decision
making about selecting the most appropriate pain management approach to ensure
high-quality care. For recommendations and strategies to optimize
patient-clinician communication, see Patient-Clinician Communication: American
Society of Clinical Oncology Consensus Guideline.264

HEALTH DISPARITIES
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE
QUESTIONSMETHODSRESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF
INTER...DISCUSSIONPATIENT AND CLINICIAN COM...HEALTH DISPARITIES <<GUIDELINE
IMPLEMENTATION ...OPEN COMMENT REVIEWLIMITATIONS OF THE RESEAR...FUTURE
DIRECTIONSADDITIONAL RESOURCESREFERENCES


Although SIO-ASCO clinical practice guidelines represent expert recommendations
on the best practices in disease management to provide the highest level of
cancer care, it is important to note that many patients have limited access to
medical care or receive fragmented care. Demographic factors such as race and
ethnicity, age, socioeconomic status, sexual orientation and gender identity,
geographic location of residence, immigrant status, insurance access, and other
social determinants are known to affect cancer care outcomes.265 The impact of
intersectionality is often cumulative and more than simply additive,17 resulting
in knowledge gaps, limited availability to high-quality primary and specialty
care, and transportation barriers. These demographic elements are bolstered by
structural factors that maintain health inequities in marginalized communities
in the United States and other countries. In countries without universal health
care, for many patients, the quintessential barrier to health care is access to
health insurance, whether uninsured or underinsured. Since integrative medical
care generally is not covered by health insurance, and many countries with
universal health care do not provide routine integrative medical care, its
access is often limited to those who can pay the out-of-pocket costs.

This clinical practice guideline should be considered in the context of existing
health inequities and structural barriers to access to care. Health care
professionals should strive to deliver the highest level of cancer care to all
populations including those who have traditionally been marginalized and
underserved. Future trials should critically evaluate inclusion and exclusion
criteria to avoid, when possible, excluding patients with comorbid conditions,
usually more prevalent among minority patients, to avoid systematically
excluding patients traditionally under-represented in clinical trials.266
Thoughtful design with regard to inclusion and exclusion criteria and
recruitment procedures will enhance sample representativeness and maximize
generalizability to diverse and under-represented patients. Moreover, trial
participation often systematically disadvantages marginalized individuals as
participation often requires frequent clinic visits, only offers interventions
during work hours, and does not provide funding for transportation, parking,
and/or childcare. Additionally, stakeholders should work toward achieving health
equity by ensuring equitable access to both high-quality cancer care and
research and addressing the structural barriers that uphold inequities in health
and health care.265

GUIDELINE IMPLEMENTATION AND POTENTIAL BARRIERS
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE
QUESTIONSMETHODSRESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF
INTER...DISCUSSIONPATIENT AND CLINICIAN COM...HEALTH DISPARITIESGUIDELINE
IMPLEMENTATION ... <<OPEN COMMENT REVIEWLIMITATIONS OF THE RESEAR...FUTURE
DIRECTIONSADDITIONAL RESOURCESREFERENCES


SIO-ASCO guidelines are developed for implementation across oncology care
settings. Patient, provider, and health system barriers exist for the
implementation of this guideline. First, patients and health care providers
often lack the knowledge and awareness of the evidence base of integrative
medicine for pain. Second, despite the recent growth of integrative medicine
programs in comprehensive cancer centers,11 these clinical services may not be
as available in community hospitals, especially hospitals serving low income,
racial, or ethnic minority populations.267 Third, oncology patients often have
medical complexity (such as neutropenia, thrombocytopenia, or presence of tumor
or surgical wound), which community integrative health providers (eg,
acupuncturists and massage therapists) may not have the necessary knowledge of
or competency to ensure safe and effective care.268 Finally, although many
nonpharmacologic integrative medicine interventions have relatively low cost,
they generally are not covered by health insurance.269

The 2012 National Health Interview Survey in the United States found that most
adults who saw a practitioner for acupuncture or massage therapy did not have
health insurance coverage for these interventions, and those with coverage were
more likely to have costs only partly covered.270 Given the financial toxicity
experienced by many patients with cancer,271 additional out-of-pocket expenses
represent significant barriers to implementation of these recommendations. The
guideline Bottom Line Box was designed to facilitate implementation of
recommendations. This guideline will be distributed widely through the SIO and
ASCO guideline information networks. Joint SIO and ASCO guidelines are posted on
the SIO and ASCO websites and are published in the Journal of Clinical Oncology.

OPEN COMMENT REVIEW
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE
QUESTIONSMETHODSRESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF
INTER...DISCUSSIONPATIENT AND CLINICIAN COM...HEALTH DISPARITIESGUIDELINE
IMPLEMENTATION ...OPEN COMMENT REVIEW <<LIMITATIONS OF THE RESEAR...FUTURE
DIRECTIONSADDITIONAL RESOURCESREFERENCES


The draft recommendations were released to the public for open comment from
November 10 through November 23, 2021, with invitations sent out to 24
organizations. There were eight respondents in total representing medical
oncology (3), integrative oncology (2), surgical oncology (1), family medicine
(1), and nursing (1). Response categories of “Agree as written,” “Agree with
suggested modifications” and “Disagree. See comments” were captured for every
proposed recommendation with 42 written comments received. A total of 80%-91% of
the responses either agreed or agreed with slight modifications to the
recommendations, while 9% of responses disagreed. Expert Panel members reviewed
comments from all sources and determined whether to maintain original draft
recommendations, revise with minor language changes, or consider major
recommendation revisions. All changes were incorporated before the SIO Clinical
Practice Guidelines Committee and ASCO Evidence Based Medicine Committee review
and approval.

LIMITATIONS OF THE RESEARCH
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE
QUESTIONSMETHODSRESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF
INTER...DISCUSSIONPATIENT AND CLINICIAN COM...HEALTH DISPARITIESGUIDELINE
IMPLEMENTATION ...OPEN COMMENT REVIEWLIMITATIONS OF THE RESEAR... <<FUTURE
DIRECTIONSADDITIONAL RESOURCESREFERENCES


The methodologic rigor is limited in some of the studies included. For mind-body
interventions, adequate blinding is often difficult, if not impossible. In
addition, the interventions often vary in dosing and format, and fidelity of the
interventions is not always monitored. For natural product interventions, the
quality of products is often not well characterized, and the dosing is rarely
standardized. The methods used to assess pain are often inconsistent among
trials, which created difficulties in interpreting the data.269 Because many
integrative medicine intervention studies do not receive funding from industry,
a large RCT of a specific intervention (eg, acupuncture) for a specific outcome
(eg, AI-related joint pain, or massage for pain in palliative care setting) is
often limited to one large trial, which does not allow for adequate replication
of data. Additionally, most of the studies failed to report any adverse events
from these interventions. Furthermore, our guideline methodology excluded
nonrandomized pragmatic studies, which may be more reflective of real-life
integrative oncology practice.272

FUTURE DIRECTIONS
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE
QUESTIONSMETHODSRESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF
INTER...DISCUSSIONPATIENT AND CLINICIAN COM...HEALTH DISPARITIESGUIDELINE
IMPLEMENTATION ...OPEN COMMENT REVIEWLIMITATIONS OF THE RESEAR...FUTURE
DIRECTIONS <<ADDITIONAL RESOURCESREFERENCES


SIO and ASCO believe that cancer clinical trials are vital to inform clinical
decisions and improve cancer care, and that all patients should have the
opportunity to participate in these trials. As this guideline has identified
scientific gaps in a number of mind-body interventions (eg, meditation, yoga,
and music) for pain management in specific populations (eg, postsurgical,
radiation, and pediatric), careful intervention development, testing, and
well-designed and executed RCTs are needed to increase the evidence base. Where
the results were mixed (eg, meditation for post-treatment survivorship pain),
additional large-scale trials and meta-analyses are needed to resolve ambiguity
stemming from the presence of both positive and negative trials. Despite
tremendous patient interest, no herbs or natural supplements can currently be
recommended for treatment of pain; thus, well-designed, placebo-controlled phase
I-III trials are needed to establish the safety and efficacy of high-quality
natural products for pain.

For treatments such as acupuncture, massage, or reflexology where there is an
existing evidence base, there is a need for hybrid trials using appropriate
implementation research frameworks and measures to determine optimal
implementation and integration of these interventions into community oncology
practices. It is particularly important to conduct trials that address the needs
of underserved patients with cancer and survivors (eg, racial and/or ethnic
minority, rural, older, pediatric, adolescent, and young adult).
Patient-centered outcomes research, comparative effectiveness trials, and
real-world trials are especially beneficial for comparing the relative benefits
and harms of different integrative medicine treatments and other appropriate
pharmacologic, behavioral, or rehabilitative treatments, so patients and
clinicians can choose among evidence-based approaches to manage pain.

Finally, with advances in omics technology, wearable sensors, behavioral and
neuroscience, big data, and novel trial designs, research needs to guide
precision integrative pain management so that the right patient receives the
right treatment to improve their pain and related outcomes.

Society for Integrative Oncology and ASCO believe that cancer clinical trials
are vital to inform clinical decisions and improve cancer care, and that all
patients should have the opportunity to participate.

ADDITIONAL RESOURCES
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE
QUESTIONSMETHODSRESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF
INTER...DISCUSSIONPATIENT AND CLINICIAN COM...HEALTH DISPARITIESGUIDELINE
IMPLEMENTATION ...OPEN COMMENT REVIEWLIMITATIONS OF THE RESEAR...FUTURE
DIRECTIONSADDITIONAL RESOURCES <<REFERENCES


More information, including a supplement with additional evidence tables, slide
sets, and clinical tools and resources, is available at
www.asco.org/survivorship-guidelines and
https://integrativeonc.org/practice-guidelines/guidelines. Patient information
is available at www.cancer.net and
https://integrativeonc.org/knowledge-center/patients.

RELATED SOCIETY FOR INTEGRATIVE ONCOLOGY AND ASCO GUIDELINES



 * Clinical practice guidelines on the evidence-based use of integrative
   therapies during and after breast cancer treatment273
   (https://acsjournals.onlinelibrary.wiley.com/doi/full/10.3322/caac.21397)

 * Complementary therapies and integrative medicine in lung cancer: Diagnosis
   and management of lung cancer, 3rd ed: American College of Chest Physicians
   evidence-based clinical practice guidelines274
   (https://pubmed.ncbi.nlm.nih.gov/23649450/)

 * Evidence-Based Clinical Practice Guidelines for Integrative Oncology:
   Complementary Therapies and Botanicals275
   (https://integrativeonc.org/docman-library/docs/65-sio-guidelines-2009/file)

 * Patient-Clinician Communication264
   (http://ascopubs.org/doi/10.1200/JCO.2017.75.2311)

 * Integrative Therapies During and After Breast Cancer Treatment276
   (https://ascopubs.org/doi/10.1200/JCO.2018.79.2721)

 * Management of Chronic Pain in Survivors of Adult Cancers2
   (https://ascopubs.org/doi/10.1200/JCO.2016.68.5206)

 * Prevention and Management of Chemotherapy-Induced Peripheral Neuropathy in
   Survivors of Adult Cancers23 (https://ascopubs.org/doi/10.1200/JCO.20.01399)



© 2022 by American Society of Clinical Oncology

Society for Integrative Oncology Clinical Practice Guidelines Committee
approval: May 6, 2022.

ASCO Evidence Based Medicine Committee approval: May 20, 2022.

EDITOR'S NOTE


This joint Society for Integrative Oncology (SIO) and ASCO Clinical Practice
Guideline provides recommendations, with comprehensive review and analyses of
the relevant literature for each recommendation. Additional information,
including a supplement with additional evidence tables, slide sets, clinical
tools and resources, and links to patient information, is available at
https://integrativeonc.org/knowledge-center/patients and www.cancer.net,
https://integrativeonc.org/practice-guidelines/guidelines and
www.asco.org/survivorship-guidelines.

SUPPORT

Supported by a generous grant from the Samueli Foundation to the Society for
Integrative Oncology to develop clinical practice guidelines.

AUTHOR CONTRIBUTIONS


Conception and design: All authors

Collection and assembly of data: All authors

Data analysis and interpretation: All authors

Manuscript writing: All authors

Final approval of manuscript: All authors

Accountable for all aspects of the work: All authors

AUTHORS' DISCLOSURES OF POTENTIAL CONFLICTS OF INTEREST

Integrative Medicine for Pain Management in Oncology: Society for Integrative
Oncology–ASCO Guideline

The following represents disclosure information provided by authors of this
manuscript. All relationships are considered compensated unless otherwise noted.
Relationships are self-held unless noted. I = Immediate Family Member, Inst = My
Institution. Relationships may not relate to the subject matter of this
manuscript. For more information about ASCO's conflict of interest policy,
please refer to www.asco.org/rwc or ascopubs.org/jco/authors/author-center.

Open Payments is a public database containing information reported by companies
about payments made to US-licensed physicians (Open Payments).

Jun J. Mao

Research Funding: Tibet Cheezheng Tibetan Medicine Co Ltd (Inst)

Nofisat Ismaila

Employment: GlaxoSmithKline (I)

Stock and Other Ownership Interests: GlaxoSmithKline (I)

Ting Bao

Research Funding: Merck

Eric L. Garland

Consulting or Advisory Role: BehaVR LLC

Patents, Royalties, Other Intellectual Property: I am a licensor to BehaVR LLC,
I have licensed my Mindfulness-Oriented Recovery Enhancement intervention to
BehaVR so the company could develop a virtual reality version of the therapy. I
receive royalties for this license.

Other Relationship: Myself

Thomas Leblanc

Honoraria: AbbVie, Astellas Pharma, Agilix

Consulting or Advisory Role: Pfizer, AbbVie/Genentech, AstraZeneca, Flatiron
Health, Bristol Myers Squibb/Celgene, GlaxoSmithKline, Astellas Pharma, Blue
Note Therapeutics

Speakers' Bureau: Agios, AbbVie, Bristol Myers Squibb/Celgene

Research Funding: AstraZeneca (Inst), Jazz Pharmaceuticals (Inst), Bristol Myers
Squibb (Inst)

Patents, Royalties, Other Intellectual Property: UpToDate Inc, royalty

Travel, Accommodations, Expenses: Agios, AbbVie/Genentech, Bristol Myers
Squibb/Celgene

Richard T. Lee

Research Funding: Merck (Inst), Incyte (Inst), Yivia (Inst)

Uncompensated Relationships: Grow Ohio Pharmaceuticals

Ana Maria Lopez

Research Funding: Bristol Myers Squibb

Charles Loprinzi

Consulting or Advisory Role: PledPharma, Metys Pharmaceuticals, Disarm
Therapeutics, OnQuality Pharmaceuticals, NKMax, Mitsubishi Tanabe Pharma,
Veloxis, Hengrui Pharmaceutical, Osmol Therapeutics, Grunenthal, Neuropathix,
Denali Therapeutics

Research Funding: Bristol Myers Squibb (Inst)

Other Relationship: Cynosure/Hologic

Gary H. Lyman

Honoraria: Sandoz, Partners Healthcare, Squibb, Seattle Genetics, Teva, Jazz
Pharmaceuticals

Consulting or Advisory Role: G1 Therapeutics, Samsung Bioepis, BeyondSpring
Pharmaceuticals, MSD, Fresenius Kabi

Research Funding: Amgen (Inst)

Viraj A. Master

Honoraria: Ethicon

Kavitha Ramchandran

Consulting or Advisory Role: Drishti, Group Well, Varian Medical Systems

Lynne I. Wagner

Stock and Other Ownership Interests: Johnson & Johnson (I), Lilly (I), Gilead
Sciences (I)

Consulting or Advisory Role: Celgene, Athenex

Travel, Accommodations, Expenses: Celgene

Deborah Watkins Bruner

Employment: Emory University

Stock and Other Ownership Interests: AbbVie, Altria, Bristol Myers Squibb,
GlaxoSmithKline, Johnson & Johnson, Pfizer, Procter & Gamble, Stryker, Viatris,
Walgreens Boots Alliance

Honoraria: American Society of Radiation Oncology (ASTRO), Oncology Nursing
Society, Memorial Sloan-Kettering Cancer Center, Alliance, Wilmont Cancer Center

Consulting or Advisory Role: Flatiron Health, Alliance for Clinical Trials in
Oncology, University of Rochester

Claudia M. Witt

Research Funding: CERES (Inst), Newsenselab (Inst)

Eduardo Bruera

Research Funding: PharmaCann Inc (Inst)

No other potential conflicts of interest were reported.

APPENDIX


TABLE A1. Recommendation Rating Definitions


View larger version (689K)



TABLE A2. Society for Integrative Oncology–ASCO Integrative Medicine for Pain
Management in Oncology Guideline Expert Panel Membership


View larger version (641K)




ACKNOWLEDGMENT

The Expert Panel wishes to thank the ASCO EBMC reviewers Drs Elise Kohn and
Michele Halyard, the ASCO Evidence Based Medicine Committee, and the SIO
Clinical Practice Guideline Committee for their thoughtful reviews and
insightful comments on this guideline.

REFERENCES
Section:
ChooseTop of pageAbstractINTRODUCTIONGUIDELINE
QUESTIONSMETHODSRESULTSRECOMMENDATIONSEVIDENCE SUMMARY OF
INTER...DISCUSSIONPATIENT AND CLINICIAN COM...HEALTH DISPARITIESGUIDELINE
IMPLEMENTATION ...OPEN COMMENT REVIEWLIMITATIONS OF THE RESEAR...FUTURE
DIRECTIONSADDITIONAL RESOURCESREFERENCES <<


1. Paice JA, Ferrell B: The management of cancer pain. CA Cancer J Clin
61:157-182, 2011 Crossref, Medline, Google Scholar2. Paice JA, Portenoy R,
Lacchetti C, et al: Management of chronic pain in survivors of adult cancers:
American Society of Clinical Oncology clinical practice guideline. J Clin Oncol
34:3325-3345, 2016 Link, Google Scholar3. Bruera E, Kim HN: Cancer pain. JAMA
290:2476-2479, 2003 Crossref, Medline, Google Scholar4. Glare PA, Davies PS,
Finlay E, et al: Pain in cancer survivors. J Clin Oncol 32:1739-1747, 2014
Link, Google Scholar5. American Cancer Society: Cancer Facts & Figures 2020.
Atlanta, GA, American Cancer Society, 2020 Google Scholar6. Mao JJ, Armstrong K,
Bowman MA, et al: Symptom burden among cancer survivors: Impact of age and
comorbidity. J Am Board Fam Med 20:434-443, 2007 Crossref, Medline, Google
Scholar7. Chim K, Xie SX, Stricker CT, et al: Joint pain severity predicts
premature discontinuation of aromatase inhibitors in breast cancer survivors.
BMC Cancer 13:401, 2013 Crossref, Medline, Google Scholar8. Brier MJ, Chambless
DL, Gross R, et al: Perceived barriers to treatment predict adherence to
aromatase inhibitors among breast cancer survivors. Cancer 123:169-176, 2017
Crossref, Medline, Google Scholar9. Witt CM, Balneaves LG, Cardoso MJ, et al: A
comprehensive definition for integrative oncology. J Natl Cancer Inst Monogr
2017, 2017 Google Scholar10. Brauer JA, El Sehamy A, Metz JM, et al:
Complementary and alternative medicine and supportive care at leading cancer
centers: A systematic analysis of websites. J Altern Complement Med 16:183-186,
2010 Crossref, Medline, Google Scholar11. Yun H, Sun L, Mao JJ: Growth of
integrative medicine at leading cancer centers between 2009 and 2016: A
systematic analysis of NCI-designated comprehensive cancer center websites. J
Natl Cancer Inst Monogr 2017:lgx004, 2017 Crossref, Google Scholar12. Mao JJ,
Farrar JT, Xie SX, et al: Use of complementary and alternative medicine and
prayer among a national sample of cancer survivors compared to other populations
without cancer. Complement Ther Med 15:21-29, 2007 Crossref, Medline, Google
Scholar13. Mao JJ, Palmer CS, Healy KE, et al: Complementary and alternative
medicine use among cancer survivors: A population-based study. J Cancer Surviv
5:8-17, 2011 Crossref, Medline, Google Scholar14. John GM, Hershman DL, Falci L,
et al: Complementary and alternative medicine use among US cancer survivors. J
Cancer Surviv 10:850-864, 2016 Crossref, Medline, Google Scholar15. Mao JJ,
Palmer SC, Straton JB, et al: Cancer survivors with unmet needs were more likely
to use complementary and alternative medicine. J Cancer Surviv 2:116-124, 2008
Crossref, Medline, Google Scholar16. Bauml J, Langer CJ, Evans T, et al: Does
perceived control predict complementary and alternative medicine (CAM) use among
patients with lung cancer? A cross-sectional survey. Support Care Cancer
22:2465-2472, 2014 Crossref, Medline, Google Scholar17. Bauml JM, Chokshi S,
Schapira MM, et al: Do attitudes and beliefs regarding complementary and
alternative medicine impact its use among patients with cancer? A
cross-sectional survey. Cancer 121:2431-2438, 2015 Crossref, Medline, Google
Scholar18. Latte-Naor S, Sidlow R, Sun L, et al: Influence of family on expected
benefits of complementary and alternative medicine (CAM) in cancer patients.
Support Care Cancer 26:2063-2069, 2018 Crossref, Medline, Google Scholar19.
Hershman DL, Unger JM, Greenlee H, et al: Effect of acupuncture vs sham
acupuncture or waitlist control on joint pain related to aromatase inhibitors
among women with early-stage breast cancer: A randomized clinical trial. JAMA
320:167-176, 2018 Crossref, Medline, Google Scholar20. Mao JJ, Liou KT, Baser
RE, et al: Effectiveness of electroacupuncture or auricular acupuncture vs usual
care for chronic musculoskeletal pain among cancer survivors: The PEACE
randomized clinical trial. JAMA Oncol 7:720-727, 2021 Crossref, Medline, Google
Scholar21. Kutner JS, Smith MC, Corbin L, et al: Massage therapy versus simple
touch to improve pain and mood in patients with advanced cancer: A randomized
trial. Ann Intern Med 149:369-379, 2008 Crossref, Medline, Google Scholar22.
Latte-Naor S, Mao JJ: Putting integrative oncology into practice: Concepts and
approaches. J Oncol Pract 15:7-14, 2019 Link, Google Scholar23. Loprinzi CL,
Lacchetti C, Bleeker J, et al: Prevention and management of chemotherapy-induced
peripheral neuropathy in survivors of adult cancers: ASCO guideline update. J
Clin Oncol 38:3325-3348, 2020 Link, Google Scholar24. Dowell D, Haegerich TM,
Chou R: CDC guideline for prescribing opioids for chronic pain—United States,
2016. MMWR Recomm Rep 65:1-49, 2016 Crossref, Medline, Google Scholar25.
Shiffman RN, Michel G, Rosenfeld RM, et al: Building better guidelines with
BRIDGE-Wiz: Development and evaluation of a software assistant to promote
clarity, transparency, and implementability. J Am Med Inform Assoc 19:94-101,
2012 Crossref, Medline, Google Scholar26. Higgins JPT, Altman DG, Gøtzsche PC,
et al: The Cochrane Collaboration's tool for assessing risk of bias in
randomised trials. BMJ 343:d5928, 2011 Crossref, Medline, Google Scholar27. Bae
K, Yoo HS, Lamoury G, et al: Acupuncture for aromatase inhibitor-induced
arthralgia: A systematic review. Integr Cancer Ther 14:496-502, 2015 Crossref,
Medline, Google Scholar28. Chen L, Lin CC, Huang TW, et al: Effect of
acupuncture on aromatase inhibitor-induced arthralgia in patients with breast
cancer: A meta-analysis of randomized controlled trials. Breast 33:132-138, 2017
Crossref, Medline, Google Scholar29. Chien TJ, Liu CY, Chang YF, et al:
Acupuncture for treating aromatase inhibitor-related arthralgia in breast
cancer: A systematic review and meta-analysis. J Altern Complement Med
21:251-260, 2015 Crossref, Medline, Google Scholar30. Pan Y, Yang K, Shi X, et
al: Clinical benefits of acupuncture for the reduction of hormone
therapy-related side effects in breast cancer patients: A systematic review.
Integr Cancer Ther 17:602-618, 2018 Crossref, Medline, Google Scholar31. Chien
TJ, Liu CY, Fang CJ, et al: The efficacy of acupuncture in chemotherapy-induced
peripheral neuropathy: Systematic review and meta-analysis. Integr Cancer Ther
18:1534735419886662, 2019 Crossref, Google Scholar32. Li K, Giustini D, Seely D:
A systematic review of acupuncture for chemotherapy-induced peripheral
neuropathy. Curr Oncol 26:e147-e154, 2019 Crossref, Medline, Google Scholar33.
Calcagni N, Gana K, Quintard B: A systematic review of complementary and
alternative medicine in oncology: Psychological and physical effects of
manipulative and body-based practices. PLoS One 14:e0223564, 2019 Crossref,
Medline, Google Scholar34. Chiu HY, Hsieh YJ, Tsai PS: Systematic review and
meta-analysis of acupuncture to reduce cancer-related pain. Eur J Cancer Care
(Engl) 26, 2017 Crossref, Medline, Google Scholar35. Choi TY, Lee MS, Kim TH, et
al: Acupuncture for the treatment of cancer pain: A systematic review of
randomised clinical trials. Support Care Cancer 20:1147-1158, 2012 Crossref,
Medline, Google Scholar36. Garcia MK, McQuade J, Haddad R, et al: Systematic
review of acupuncture in cancer care: A synthesis of the evidence. J Clin Oncol
31:952-960, 2013 Link, Google Scholar37. Lau CH, Wu X, Chung VC, et al:
Acupuncture and related therapies for symptom management in palliative cancer
care: Systematic review and meta-analysis. Medicine (Baltimore) 95:e2901, 2016
Crossref, Medline, Google Scholar38. Lee H, Schmidt K, Ernst E: Acupuncture for
the relief of cancer-related pain—A systematic review. Eur J Pain 9:437-444,
2005 Crossref, Medline, Google Scholar39. Lian WL, Pan MQ, Zhou DH, et al:
Effectiveness of acupuncture for palliative care in cancer patients: A
systematic review. Chin J Integr Med 20:136-147, 2014 Crossref, Medline, Google
Scholar40. Lopes-Júnior LC, Rosa GS, Pessanha RM, et al: Efficacy of the
complementary therapies in the management of cancer pain in palliative care: A
systematic review. Rev Lat Am Enfermagem 28:e3377, 2020 Crossref,
Medline, Google Scholar41. Paley CA, Johnson MI, Tashani OA, et al: Acupuncture
for cancer pain in adults. Cochrane Database Syst Rev 2015:CD007753, 2015 Google
Scholar42. Tao WW, Jiang H, Tao XM, et al: Effects of acupuncture, Tuina, Tai
Chi, Qigong, and traditional Chinese medicine five-element music therapy on
symptom management and quality of life for cancer patients: A meta-analysis. J
Pain Symptom Manage 51:728-747, 2016 Crossref, Medline, Google Scholar43. He Y,
Guo X, May BH, et al: Clinical evidence for association of acupuncture and
acupressure with improved cancer pain: A systematic review and meta-analysis.
JAMA Oncol 6:271-278, 2020 Crossref, Medline, Google Scholar44. Bao T, Cai L,
Giles JT, et al: A dual-center randomized controlled double blind trial
assessing the effect of acupuncture in reducing musculoskeletal symptoms in
breast cancer patients taking aromatase inhibitors. Breast Cancer Res Treat
138:167-174, 2013 Crossref, Medline, Google Scholar45. Crew KD, Capodice JL,
Greenlee H, et al: Randomized, blinded, sham-controlled trial of acupuncture for
the management of aromatase inhibitor-associated joint symptoms in women with
early-stage breast cancer. J Clin Oncol 28:1154-1160, 2010 Link, Google
Scholar46. Mao JJ, Xie SX, Farrar JT, et al: A randomised trial of
electro-acupuncture for arthralgia related to aromatase inhibitor use. Eur J
Cancer 50:267-276, 2014 Crossref, Medline, Google Scholar47. Oh B, Kimble B,
Costa DS, et al: Acupuncture for treatment of arthralgia secondary to aromatase
inhibitor therapy in women with early breast cancer: Pilot study. Acupunct Med
31:264-271, 2013 Crossref, Medline, Google Scholar48. Alimi D, Rubino C,
Pichard-Léandri E, et al: Analgesic effect of auricular acupuncture for cancer
pain: A randomized, blinded, controlled trial. J Clin Oncol 21:4120-4126, 2003
Link, Google Scholar49. Chen H, Liu TY, Kuai L, et al: Electroacupuncture
treatment for pancreatic cancer pain: A randomized controlled trial.
Pancreatology 13:594-597, 2013 Crossref, Medline, Google Scholar50. Kim K, Lee
S: Intradermal acupuncture along with analgesics for pain control in advanced
cancer cases: A pilot, randomized, patient-assessor-blinded, controlled trial.
Integr Cancer Ther 17:1137-1143, 2018 Crossref, Medline, Google Scholar51. Lam
TY, Lu LM, Ling WM, et al: A pilot randomized controlled trial of acupuncture at
the Si Guan Xue for cancer pain. BMC Complement Altern Med 17:335, 2017
Crossref, Medline, Google Scholar52. Sharif Nia H, Pahlevan Sharif S,
Yaghoobzadeh A, et al: Effect of acupressure on pain in Iranian leukemia
patients: A randomized controlled trial study. Int J Nurs Pract 23, 2017
Crossref, Medline, Google Scholar53. Xu LP, Yang SL, Su SQ, et al: Effect of
wrist-ankle acupuncture therapy combined with auricular acupuncture on cancer
pain: A four-parallel arm randomized controlled trial. Complement Ther Clin
Pract 39:101170, 2020 Crossref, Medline, Google Scholar54. Yeh CH, Chien LC, Lin
WC, et al: Pilot randomized controlled trial of auricular point acupressure to
manage symptom clusters of pain, fatigue, and disturbed sleep in breast cancer
patients. Cancer Nurs 39:402-410, 2016 Crossref, Medline, Google Scholar55.
Ruela LO, Iunes DH, Nogueira DA, et al: Effectiveness of auricular acupuncture
in the treatment of cancer pain: Randomized clinical trial. Rev Esc Enferm USP
52:e03402, 2018 Medline, Google Scholar56. Han X, Wang L, Shi H, et al:
Acupuncture combined with methylcobalamin for the treatment of
chemotherapy-induced peripheral neuropathy in patients with multiple myeloma.
BMC Cancer 17:40, 2017 Crossref, Medline, Google Scholar57. Iravani S, Kazemi
Motlagh AH, Emami Razavi SZ, et al: Effectiveness of acupuncture treatment on
chemotherapy-induced peripheral neuropathy: A pilot, randomized,
assessor-blinded, controlled trial. Pain Res Manag 2020:2504674, 2020 Crossref,
Medline, Google Scholar58. Molassiotis A, Suen LKP, Cheng HL, et al: A
randomized assessor-blinded wait-list-controlled trial to assess the
effectiveness of acupuncture in the management of chemotherapy-induced
peripheral neuropathy. Integr Cancer Ther 18:1534735419836501, 2019
Crossref, Google Scholar59. Rostock M, Jaroslawski K, Guethlin C, et al:
Chemotherapy-induced peripheral neuropathy in cancer patients: A four-arm
randomized trial on the effectiveness of electroacupuncture. Evid Based
Complement Alternat Med 2013:349653, 2013 Crossref, Medline, Google Scholar60.
Lu W, Giobbie-Hurder A, Freedman RA, et al: Acupuncture for chemotherapy-induced
peripheral neuropathy in breast cancer survivors: A randomized controlled pilot
trial. Oncologist 25:310-318, 2020 Crossref, Medline, Google Scholar61. Zhang S,
Wu T, Zhang H, et al: Effect of electroacupuncture on chemotherapy-induced
peripheral neuropathy in patients with malignant tumor: A single-blinded,
randomized controlled trial. J Tradit Chin Med 37:179-184, 2017 Crossref,
Medline, Google Scholar62. Bao T, Patil S, Chen C, et al: Effect of acupuncture
vs sham procedure on chemotherapy-induced peripheral neuropathy symptoms: A
randomized clinical trial. JAMA Netw Open 3:e200681, 2020 Crossref,
Medline, Google Scholar63. Greenlee H, Crew KD, Capodice J, et al: Randomized
sham-controlled pilot trial of weekly electro-acupuncture for the prevention of
taxane-induced peripheral neuropathy in women with early stage breast cancer.
Breast Cancer Res Treat 156:453-464, 2016 Crossref, Medline, Google Scholar64.
Bao T, Ye X, Skinner J, et al: The analgesic effect of magnetic acupressure in
cancer patients undergoing bone marrow aspiration and biopsy: A randomized,
blinded, controlled trial. J Pain Symptom Manage 41:995-1002, 2011 Crossref,
Medline, Google Scholar65. Sharifi Rizi M, Shamsalinia A, Ghaffari F, et al: The
effect of acupressure on pain, anxiety, and the physiological indexes of
patients with cancer undergoing bone marrow biopsy. Complement Ther Clin Pract
29:136-141, 2017 Crossref, Medline, Google Scholar66. Quinlan-Woodward J, Gode
A, Dusek JA, et al: Assessing the impact of acupuncture on pain, nausea,
anxiety, and coping in women undergoing a mastectomy. Oncol Nurs Forum
43:725-732, 2016 Crossref, Medline, Google Scholar67. Deng G, Rusch V, Vickers
A, et al: Randomized controlled trial of a special acupuncture technique for
pain after thoracotomy. J Thorac Cardiovasc Surg 136:1464-1469, 2008 Crossref,
Medline, Google Scholar68. Hsiung WT, Chang YC, Yeh ML, et al: Acupressure
improves the postoperative comfort of gastric cancer patients: A randomised
controlled trial. Complement Ther Med 23:339-346, 2015 Crossref, Medline, Google
Scholar69. Mehling WE, Jacobs B, Acree M, et al: Symptom management with massage
and acupuncture in postoperative cancer patients: A randomized controlled trial.
J Pain Symptom Manage 33:258-266, 2007 Crossref, Medline, Google Scholar70.
Pfister DG, Cassileth BR, Deng GE, et al: Acupuncture for pain and dysfunction
after neck dissection: Results of a randomized controlled trial. J Clin Oncol
28:2565-2570, 2010 Link, Google Scholar71. Wong RH, Lee TW, Sihoe AD, et al:
Analgesic effect of electroacupuncture in postthoracotomy pain: A prospective
randomized trial. Ann Thorac Surg 81:2031-2036, 2006 Crossref, Medline, Google
Scholar72. Zeng K, Dong HJ, Chen HY, et al: Wrist-ankle acupuncture for pain
after transcatheter arterial chemoembolization in patients with liver cancer: A
randomized controlled trial. Am J Chin Med 42:289-302, 2014 Crossref,
Medline, Google Scholar73. Giron PS, Haddad CA, Lopes de Almeida Rizzi SK, et
al: Effectiveness of acupuncture in rehabilitation of physical and functional
disorders of women undergoing breast cancer surgery. Support Care Cancer
24:2491-2496, 2016 Crossref, Medline, Google Scholar74. Deng G, Giralt S, Chung
DJ, et al: Reduction of opioid use by acupuncture in patients undergoing
hematopoietic stem cell transplantation: Secondary analysis of a randomized,
sham-controlled trial. Pain Med 21:636-642, 2020 Crossref, Medline, Google
Scholar75. Dilaveri CA, Croghan IT, Mallory MJ, et al: Massage compared with
massage plus acupuncture for breast cancer patients undergoing reconstructive
surgery. J Altern Complement Med 26:602-609, 2020 Crossref, Medline, Google
Scholar76. Adair M, Murphy B, Yarlagadda S, et al: Feasibility and preliminary
efficacy of tailored yoga in survivors of head and neck cancer: A pilot study.
Integr Cancer Ther 17:774-784, 2018 Crossref, Medline, Google Scholar77. Eyigor
S, Uslu R, Apaydın S, et al: Can yoga have any effect on shoulder and arm pain
and quality of life in patients with breast cancer? A randomized, controlled,
single-blind trial. Complement Ther Clin Pract 32:40-45, 2018 Crossref,
Medline, Google Scholar78. Huberty J, Eckert R, Dueck A, et al: Online yoga in
myeloproliferative neoplasm patients: Results of a randomized pilot trial to
inform future research. BMC Complement Altern Med 19:121, 2019 Crossref,
Medline, Google Scholar79. Porter LS, Carson JW, Olsen M, et al: Feasibility of
a mindful yoga program for women with metastatic breast cancer: Results of a
randomized pilot study. Support Care Cancer 27:4307-4316, 2019 Crossref,
Medline, Google Scholar80. Charalambous A, Giannakopoulou M, Bozas E, et al:
Guided imagery and progressive muscle relaxation as a cluster of symptoms
management intervention in patients receiving chemotherapy: A randomized control
trial. PLoS One 11:e0156911, 2016 Crossref, Medline, Google Scholar81. Sloman R,
Brown P, Aldana E, et al: The use of relaxation for the promotion of comfort and
pain relief in persons with advanced cancer. Contemp Nurse 3:6-12, 1994
Crossref, Medline, Google Scholar82. Cramer H, Lauche R, Paul A, et al: Hypnosis
in breast cancer care: A systematic review of randomized controlled trials.
Integr Cancer Ther 14:5-15, 2015 Crossref, Medline, Google Scholar83. Richardson
J, Smith JE, McCall G, et al: Hypnosis for procedure-related pain and distress
in pediatric cancer patients: A systematic review of effectiveness and
methodology related to hypnosis interventions. J Pain Symptom Manage 31:70-84,
2006 Crossref, Medline, Google Scholar84. Amraoui J, Pouliquen C, Fraisse J, et
al: Effects of a hypnosis session before general anesthesia on postoperative
outcomes in patients who underwent minor breast cancer surgery: The HYPNOSEIN
randomized clinical trial. JAMA Netw Open 1:e181164, 2018 Crossref,
Medline, Google Scholar85. Montgomery GH, Bovbjerg DH, Schnur JB, et al: A
randomized clinical trial of a brief hypnosis intervention to control side
effects in breast surgery patients. J Natl Cancer Inst 99:1304-1312, 2007
Crossref, Medline, Google Scholar86. Montgomery GH, Hallquist MN, Schnur JB, et
al: Mediators of a brief hypnosis intervention to control side effects in breast
surgery patients: Response expectancies and emotional distress. J Consult Clin
Psychol 78:80-88, 2010 Crossref, Medline, Google Scholar87. Hızlı F, Özcan O,
Selvi İ, et al: The effects of hypnotherapy during transrectal ultrasound-guided
prostate needle biopsy for pain and anxiety. Int Urol Nephrol 47:1773-1777, 2015
Crossref, Medline, Google Scholar88. Lang EV, Berbaum KS, Pauker SG, et al:
Beneficial effects of hypnosis and adverse effects of empathic attention during
percutaneous tumor treatment: When being nice does not suffice. J Vasc Interv
Radiol 19:897-905, 2008 Crossref, Medline, Google Scholar89. Montgomery GH,
Weltz CR, Seltz M, et al: Brief presurgery hypnosis reduces distress and pain in
excisional breast biopsy patients. Int J Clin Exp Hypn 50:17-32, 2002 Crossref,
Medline, Google Scholar90. Snow A, Dorfman D, Warbet R, et al: A randomized
trial of hypnosis for relief of pain and anxiety in adult cancer patients
undergoing bone marrow procedures. J Psychosoc Oncol 30:281-293, 2012 Crossref,
Medline, Google Scholar91. Lang EV, Berbaum KS, Faintuch S, et al: Adjunctive
self-hypnotic relaxation for outpatient medical procedures: A prospective
randomized trial with women undergoing large core breast biopsy. Pain
126:155-164, 2006 Crossref, Medline, Google Scholar92. Dikmen HA, Terzioglu F:
Effects of reflexology and progressive muscle relaxation on pain, fatigue, and
quality of life during chemotherapy in gynecologic cancer patients. Pain Manag
Nurs 20:47-53, 2019 Crossref, Medline, Google Scholar93. Rambod M, Pasyar N,
Shamsadini M: The effect of foot reflexology on fatigue, pain, and sleep quality
in lymphoma patients: A clinical trial. Eur J Oncol Nurs 43:101678, 2019
Crossref, Medline, Google Scholar94. Sikorskii A, Niyogi PG, Victorson D, et al:
Symptom response analysis of a randomized controlled trial of reflexology for
symptom management among women with advanced breast cancer. Support Care Cancer
28:1395-1404, 2020 Crossref, Medline, Google Scholar95. Stephenson NL, Swanson
M, Dalton J, et al: Partner-delivered reflexology: Effects on cancer pain and
anxiety. Oncol Nurs Forum 34:127-132, 2007 Crossref, Medline, Google Scholar96.
Uysal N, Kutlutürkan S, Uğur I: Effects of foot massage applied in two different
methods on symptom control in colorectal cancer patients: Randomised control
trial. Int J Nurs Pract 23, 2017 Crossref, Medline, Google Scholar97. Wyatt G,
Sikorskii A, Rahbar MH, et al: Health-related quality-of-life outcomes: A
reflexology trial with patients with advanced-stage breast cancer. Oncol Nurs
Forum 39:568-577, 2012 Crossref, Medline, Google Scholar98. Wyatt G, Sikorskii
A, Tesnjak I, et al: A randomized clinical trial of caregiver-delivered
reflexology for symptom management during breast cancer treatment. J Pain
Symptom Manage 54:670-679, 2017 Crossref, Medline, Google Scholar99. Kurt S, Can
G: Reflexology in the management of chemotherapy induced peripheral neuropathy:
A pilot randomized controlled trial. Eur J Oncol Nurs 32:12-19, 2018 Crossref,
Medline, Google Scholar100. Noh GO, Park KS: Effects of aroma self-foot
reflexology on peripheral neuropathy, peripheral skin temperature, anxiety, and
depression in gynaecologic cancer patients undergoing chemotherapy: A randomised
controlled trial. Eur J Oncol Nurs 42:82-89, 2019 Crossref, Medline, Google
Scholar101. Pinheiro da Silva F, Moreira GM, Zomkowski K, et al: Manual therapy
as treatment for chronic musculoskeletal pain in female breast cancer survivors:
A systematic review and meta-analysis. J Manipulative Physiol Ther 42:503-513,
2019 Crossref, Medline, Google Scholar102. Shin ES, Seo KH, Lee SH, et al:
Massage with or without aromatherapy for symptom relief in people with cancer.
Cochrane Database Syst Rev:CD009873, 2016 Medline, Google Scholar103. Ernst E:
Massage therapy for cancer palliation and supportive care: A systematic review
of randomised clinical trials. Support Care Cancer 17:333-337, 2009 Crossref,
Medline, Google Scholar104. Post-White J, Kinney ME, Savik K, et al: Therapeutic
massage and healing touch improve symptoms in cancer. Integr Cancer Ther
2:332-344, 2003 Crossref, Medline, Google Scholar105. Weinrich SP, Weinrich MC:
The effect of massage on pain in cancer patients. Appl Nurs Res 3:140-145, 1990
Crossref, Medline, Google Scholar106. Jane SW, Chen SL, Wilkie DJ, et al:
Effects of massage on pain, mood status, relaxation, and sleep in Taiwanese
patients with metastatic bone pain: A randomized clinical trial. Pain
152:2432-2442, 2011 Crossref, Medline, Google Scholar107. Massingill J,
Jorgensen C, Dolata J, et al: Myofascial massage for chronic pain and decreased
upper extremity mobility after breast cancer surgery. Int J Ther Massage
Bodywork 11:4-9, 2018 Medline, Google Scholar108. Toth M, Marcantonio ER, Davis
RB, et al: Massage therapy for patients with metastatic cancer: A pilot
randomized controlled trial. J Altern Complement Med 19:650-656, 2013 Crossref,
Medline, Google Scholar109. Wilkie DJ, Kampbell J, Cutshall S, et al: Effects of
massage on pain intensity, analgesics and quality of life in patients with
cancer pain: A pilot study of a randomized clinical trial conducted within
hospice care delivery. Hosp J 15:31-53, 2000 Medline, Google Scholar110. Listing
M, Reisshauer A, Krohn M, et al: Massage therapy reduces physical discomfort and
improves mood disturbances in women with breast cancer. Psychooncology
18:1290-1299, 2009 Crossref, Medline, Google Scholar111. Groef AD, Kampen MV,
Vervloesem N, et al: Effect of myofascial techniques for treatment of persistent
arm pain after breast cancer treatment: Randomized controlled trial. Clin
Rehabil 32:451-461, 2018 Crossref, Medline, Google Scholar112. Burrai F,
Micheluzzi V, Bugani V: Effects of live sax music on various physiological
parameters, pain level, and mood level in cancer patients: A randomized
controlled trial. Holist Nurs Pract 28:301-311, 2014 Crossref, Medline, Google
Scholar113. Hsieh FC, Miao NF, Tseng IJ, et al: Effect of home-based music
intervention versus ambient music on breast cancer survivors in the community: A
feasibility study in Taiwan. Eur J Cancer Care (Engl) 28:e13064, 2019 Crossref,
Medline, Google Scholar114. Huang ST, Good M, Zauszniewski JA: The effectiveness
of music in relieving pain in cancer patients: A randomized controlled trial.
Int J Nurs Stud 47:1354-1362, 2010 Crossref, Medline, Google Scholar115. Arruda
MA, Garcia MA, Garcia JB: Evaluation of the effects of music and poetry in
oncologic pain relief: A randomized clinical trial. J Palliat Med 19:943-948,
2016 Crossref, Medline, Google Scholar116. Binns-Turner PG, Wilson LL, Pryor ER,
et al: Perioperative music and its effects on anxiety, hemodynamics, and pain in
women undergoing mastectomy. AANA J 79:S21-S27, 2011 Medline, Google Scholar117.
Li XM, Yan H, Zhou KN, et al: Effects of music therapy on pain among female
breast cancer patients after radical mastectomy: Results from a randomized
controlled trial. Breast Cancer Res Treat 128:411-419, 2011 Crossref,
Medline, Google Scholar118. Wang Y, Tang H, Guo Q, et al: Effects of intravenous
patient-controlled sufentanil analgesia and music therapy on pain and
hemodynamics after surgery for lung cancer: A randomized parallel study. J
Altern Complement Med 21:667-672, 2015 Crossref, Medline, Google Scholar119.
Bates D, Bolwell B, Majhail NS, et al: Music therapy for symptom management
after autologous stem cell transplantation: Results from a randomized study.
Biol Blood Marrow Transplant 23:1567-1572, 2017 Crossref, Medline, Google
Scholar120. Kwekkeboom KL: Music versus distraction for procedural pain and
anxiety in patients with cancer. Oncol Nurs Forum 30:433-440, 2003 Crossref,
Medline, Google Scholar121. Fredenburg HA, Silverman MJ: Effects of music
therapy on positive and negative affect and pain with hospitalized patients
recovering from a blood and marrow transplant: A randomized effectiveness study.
Arts Psychother 41:174-180, 2014 Crossref, Google Scholar122. Zengin S, Kabul S,
Al B, et al: Effects of music therapy on pain and anxiety in patients undergoing
port catheter placement procedure. Complement Ther Med 21:689-696, 2013
Crossref, Medline, Google Scholar123. Danhauer SC, Vishnevsky T, Campbell CR, et
al: Music for patients with hematological malignancies undergoing bone marrow
biopsy: A randomized controlled study of anxiety, perceived pain, and patient
satisfaction. J Soc Integr Oncol 8:140-147, 2010 Medline, Google Scholar124.
Warth M, Keßler J, Hillecke TK, et al: Music therapy in palliative care. Dtsch
Arztebl Int 112:788-794, 2015 Medline, Google Scholar125. Haase O, Schwenk W,
Hermann C, et al: Guided imagery and relaxation in conventional colorectal
resections: A randomized, controlled, partially blinded trial. Dis Colon Rectum
48:1955-1963, 2005 Crossref, Medline, Google Scholar126. De Paolis G, Naccarato
A, Cibelli F, et al: The effectiveness of progressive muscle relaxation and
interactive guided imagery as a pain-reducing intervention in advanced cancer
patients: A multicentre randomised controlled non-pharmacological trial.
Complement Ther Clin Pract 34:280-287, 2019 Crossref, Medline, Google
Scholar127. Ratcliff CG, Prinsloo S, Chaoul A, et al: A randomized controlled
trial of brief mindfulness meditation for women undergoing stereotactic breast
biopsy. J Am Coll Radiol 16:691-699, 2019 Crossref, Medline, Google Scholar128.
Dion LJ, Engen DJ, Lemaine V, et al: Massage therapy alone and in combination
with meditation for breast cancer patients undergoing autologous tissue
reconstruction: A randomized pilot study. Complement Ther Clin Pract 23:82-87,
2016 Crossref, Medline, Google Scholar129. Soo MS, Jarosz JA, Wren AA, et al:
Imaging-guided core-needle breast biopsy: Impact of meditation and music
interventions on patient Anxiety, pain, and fatigue. J Am Coll Radiol
13:526-534, 2016 Crossref, Medline, Google Scholar130. Wren AA, Shelby RA, Soo
MS, et al: Preliminary efficacy of a lovingkindness meditation intervention for
patients undergoing biopsy and breast cancer surgery: A randomized controlled
pilot study. Support Care Cancer 27:3583-3592, 2019 Crossref, Medline, Google
Scholar131. Lengacher CA, Reich RR, Paterson CL, et al: Examination of broad
symptom improvement resulting from mindfulness-based stress reduction in breast
cancer survivors: A randomized controlled trial. J Clin Oncol 34:2827-2834, 2016
Link, Google Scholar132. Johannsen M, O'Connor M, O'Toole MS, et al: Efficacy of
mindfulness-based cognitive therapy on late post-treatment pain in women treated
for primary breast cancer: A randomized controlled trial. J Clin Oncol
34:3390-3399, 2016 Link, Google Scholar133. Liu H, Gao X, Hou Y: Effects of
mindfulness-based stress reduction combined with music therapy on pain, anxiety,
and sleep quality in patients with osteosarcoma. Braz J Psychiatry 41:540-545,
2019 Crossref, Medline, Google Scholar134. Mendoza ME, Capafons A, Gralow JR, et
al: Randomized controlled trial of the Valencia model of waking hypnosis plus
CBT for pain, fatigue, and sleep management in patients with cancer and cancer
survivors. Psychooncology 26:1832-1838, 2017 Crossref, Medline, Google
Scholar135. Butler LD, Koopman C, Neri E, et al: Effects of
supportive-expressive group therapy on pain in women with metastatic breast
cancer. Health Psychol 28:579-587, 2009 Crossref, Medline, Google Scholar136.
Syrjala KL, Cummings C, Donaldson GW: Hypnosis or cognitive behavioral training
for the reduction of pain and nausea during cancer treatment: A controlled
clinical trial. Pain 48:137-146, 1992 Crossref, Medline, Google Scholar137.
Thuma K, Ditsataporncharoen T, Arunpongpaisal S, et al: Hypnosis as an adjunct
for managing pain in head and neck cancer patients post radiotherapy. J Med
Assoc Thai 99:S141-S147, 2016 (suppl 5) Medline, Google Scholar138. Tsay SL,
Chen HL, Chen SC, et al: Effects of reflexotherapy on acute postoperative pain
and anxiety among patients with digestive cancer. Cancer Nurs 31:109-115, 2008
Crossref, Medline, Google Scholar139. Forchuk C, Baruth P, Prendergast M, et al:
Postoperative arm massage: A support for women with lymph node dissection.
Cancer Nurs 27:25-33, 2004 Crossref, Medline, Google Scholar140. Rosen J,
Lawrence R, Bouchard M, et al: Massage for perioperative pain and anxiety in
placement of vascular access devices. Adv Mind Body Med 27:12-23, 2013
Medline, Google Scholar141. Taylor AG, Galper DI, Taylor P, et al: Effects of
adjunctive Swedish massage and vibration therapy on short-term postoperative
outcomes: A randomized, controlled trial. J Altern Complement Med 9:77-89, 2003
Crossref, Medline, Google Scholar142. Bani Mohammad E, Ahmad M: Virtual reality
as a distraction technique for pain and anxiety among patients with breast
cancer: A randomized control trial. Palliat Support Care 17:29-34, 2019
Crossref, Medline, Google Scholar143. Feyzioğlu Ö, Dinçer S, Akan A, et al: Is
Xbox 360 Kinect-based virtual reality training as effective as standard
physiotherapy in patients undergoing breast cancer surgery? Support Care Cancer
28:4295-4303, 2020 Crossref, Medline, Google Scholar144. An W, Li S, Qin L: Role
of honey in preventing radiation-induced oral mucositis: A meta-analysis of
randomized controlled trials. Food Funct 12:3352-3365, 2021 Crossref,
Medline, Google Scholar145. Lima I, e Fátima Souto Maior L, Gueiros LAM, et al:
Clinical applicability of natural products for prevention and treatment of oral
mucositis: A systematic review and meta-analysis. Clin Oral Investig
25:4115-4124, 2021 Crossref, Medline, Google Scholar146. Tian X, Xu L, Liu X, et
al: Impact of honey on radiotherapy-induced oral mucositis in patients with head
and neck cancer: A systematic review and meta-analysis. Ann Palliat Med
9:1431-1441, 2020 Crossref, Medline, Google Scholar147. Shuai T, Tian X, Xu LL,
et al: Oral glutamine may have No clinical benefits to prevent radiation-induced
oral mucositis in adult patients with head and neck cancer: A meta-analysis of
randomized controlled trials. Front Nutr 7:49, 2020 Crossref, Medline, Google
Scholar148. Abdulrhman M, Elbarbary NS, Ahmed Amin D, et al: Honey and a mixture
of honey, beeswax, and olive oil-propolis extract in treatment of
chemotherapy-induced oral mucositis: A randomized controlled pilot study.
Pediatr Hematol Oncol 29:285-292, 2012 Crossref, Medline, Google Scholar149.
Ameri A, Poshtmahi S, Heydarirad G, et al: Effect of honey-lemon spray versus
benzydamine hydrochloride spray on radiation-induced acute oral mucositis in
head and neck cancer patients: A pilot, randomized, double-blind,
active-controlled clinical trial. J Altern Complement Med 27:255-262, 2021
Crossref, Medline, Google Scholar150. Charalambous M, Raftopoulos V, Paikousis
L, et al: The effect of the use of thyme honey in minimizing radiation—Induced
oral mucositis in head and neck cancer patients: A randomized controlled trial.
Eur J Oncol Nurs 34:89-97, 2018 Crossref, Medline, Google Scholar151. Amanat A,
Ahmed A, Kazmi A, et al: The effect of honey on radiation-induced oral mucositis
in head and neck cancer patients. Indian J Palliat Care 23:317-320, 2017
Crossref, Medline, Google Scholar152. Samdariya S, Lewis S, Kauser H, et al: A
randomized controlled trial evaluating the role of honey in reducing pain due to
radiation induced mucositis in head and neck cancer patients. Indian J Palliat
Care 21:268-273, 2015 Crossref, Medline, Google Scholar153. Hawley P, Hovan A,
McGahan CE, et al: A randomized placebo-controlled trial of manuka honey for
radiation-induced oral mucositis. Support Care Cancer 22:751-761, 2014 Crossref,
Medline, Google Scholar154. Jayachandran S, Balaji N: Evaluating the
effectiveness of topical application of natural honey and benzydamine
hydrochloride in the management of radiation mucositis. Indian J Palliat Care
18:190-195, 2012 Crossref, Medline, Google Scholar155. Bardy J, Molassiotis A,
Ryder WD, et al: A double-blind, placebo-controlled, randomised trial of active
manuka honey and standard oral care for radiation-induced oral mucositis. Br J
Oral Maxillofac Surg 50:221-226, 2012 Crossref, Medline, Google Scholar156.
Khanal B, Baliga M, Uppal N: Effect of topical honey on limitation of
radiation-induced oral mucositis: An intervention study. Int J Oral Maxillofac
Surg 39:1181-1185, 2010 Crossref, Medline, Google Scholar157. Rashad UM,
Al-Gezawy SM, El-Gezawy E, et al: Honey as topical prophylaxis against
radiochemotherapy-induced mucositis in head and neck cancer. J Laryngol Otol
123:223-228, 2009 Crossref, Medline, Google Scholar158. Motallebnejad M, Akram
S, Moghadamnia A, et al: The effect of topical application of pure honey on
radiation-induced mucositis: A randomized clinical trial. J Contemp Dent Pract
9:40-47, 2008 Crossref, Medline, Google Scholar159. Rao S, Hegde SK, Rao P, et
al: Honey mitigates radiation-induced oral mucositis in head and neck cancer
patients without affecting the tumor response. Foods 6:77, 2017 Crossref, Google
Scholar160. Khanjani Pour-Fard-Pachekenari A, Rahmani A, Ghahramanian A, et al:
The effect of an oral care protocol and honey mouthwash on mucositis in acute
myeloid leukemia patients undergoing chemotherapy: A single-blind clinical
trial. Clin Oral Investig 23:1811-1821, 2019 Crossref, Medline, Google
Scholar161. Al Jaouni SK, Al Muhayawi MS, Hussein A, et al: Effects of honey on
oral mucositis among pediatric cancer patients undergoing chemo/radiotherapy
treatment at King Abdulaziz University Hospital in Jeddah, Kingdom of Saudi
Arabia. Evid Based Complement Alternat Med 2017:5861024, 2017 Crossref,
Medline, Google Scholar162. Mishra L, Nayak G: Effect of flavoured ice chips in
reduction of oral mucositis among children receiving chemotherapy. Int J Pharm
Sci Rev Res 43:25-28, 2017 Google Scholar163. Raeessi MA, Raeessi N, Panahi Y,
et al: “Coffee plus honey” versus “topical steroid” in the treatment of
chemotherapy-induced oral mucositis: A randomised controlled trial. BMC
Complement Altern Med 14:293, 2014 Crossref, Medline, Google Scholar164. Biswal
BM, Zakaria A, Ahmad NM: Topical application of honey in the management of
radiation mucositis: A preliminary study. Support Care Cancer 11:242-248, 2003
Crossref, Medline, Google Scholar165. Alvi Z, Mahmood A, Rasul S, et al: Role of
honey in prevention of radiation induced mucositis in head and neck cancer. Pak
Armed Forces Med J 63:379-383, 2013 Google Scholar166. Fogh SE, Deshmukh S, Berk
LB, et al: A randomized phase 2 trial of prophylactic manuka honey for the
reduction of chemoradiation therapy-induced esophagitis during the treatment of
lung cancer: Results of NRG oncology RTOG 1012. Int J Radiat Oncol Biol Phys
97:786-796, 2017 Crossref, Medline, Google Scholar167. Fidler P, Loprinzi CL,
O'Fallon JR, et al: Prospective evaluation of a chamomile mouthwash for
prevention of 5-FU-induced oral mucositis. Cancer 77:522-525, 1996 Crossref,
Medline, Google Scholar168. Dos Reis PE, Ciol MA, de Melo NS, et al: Chamomile
infusion cryotherapy to prevent oral mucositis induced by chemotherapy: A pilot
study. Support Care Cancer 24:4393-4398, 2016 Crossref, Medline, Google
Scholar169. Piredda M, Facchinetti G, Biagioli V, et al: Propolis in the
prevention of oral mucositis in breast cancer patients receiving adjuvant
chemotherapy: A pilot randomised controlled trial. Eur J Cancer Care (Engl) 26,
2017 Crossref, Google Scholar170. Javadzadeh Bolouri A, Pakfetrat A, Tonkaboni
A, et al: Preventing and therapeutic effect of propolis in radiotherapy induced
mucositis of head and neck cancers: A triple-blind, randomized,
placebo-controlled trial. Iran J Cancer Prev 8:e4019, 2015 Crossref,
Medline, Google Scholar171. Salehi M, Saeedi M, Ghorbani A, et al: The effect of
propolis tablet on oral mucositis caused by chemotherapy. Gazi Med J 29:196-201,
2018 Google Scholar172. Pattanayak L, Panda N, Dash MK, et al: Management of
chemoradiation-induced mucositis in head and neck cancers with oral glutamine. J
Glob Oncol 2:200-206, 2016 Link, Google Scholar173. Tsujimoto T, Yamamoto Y,
Wasa M, et al: L-Glutamine decreases the severity of mucositis induced by
chemoradiotherapy in patients with locally advanced head and neck cancer: A
double-blind, randomized, placebo-controlled trial. Oncol Rep 33:33-39, 2015
Crossref, Medline, Google Scholar174. Chattopadhyay S, Saha A, Azam M, et al:
Role of oral glutamine in alleviation and prevention of radiation-induced oral
mucositis: A prospective randomized study. South Asian J Cancer 3:8-12, 2014
Crossref, Medline, Google Scholar175. Huang CJ, Huang MY, Fang PT, et al:
Randomized double-blind, placebo-controlled trial evaluating oral glutamine on
radiation-induced oral mucositis and dermatitis in head and neck cancer
patients. Am J Clin Nutr 109:606-614, 2019 Crossref, Medline, Google Scholar176.
Tanaka Y, Takahashi T, Yamaguchi K, et al: Elemental diet plus glutamine for the
prevention of mucositis in esophageal cancer patients receiving chemotherapy: A
feasibility study. Support Care Cancer 24:933-941, 2016 Crossref,
Medline, Google Scholar177. Peterson DE, Jones JB, Petit RGII: Randomized,
placebo-controlled trial of Saforis for prevention and treatment of oral
mucositis in breast cancer patients receiving anthracycline-based chemotherapy.
Cancer 109:322-331, 2007 Crossref, Medline, Google Scholar178. Cerchietti LC,
Navigante AH, Lutteral MA, et al: Double-blinded, placebo-controlled trial on
intravenous L-alanyl-L-glutamine in the incidence of oral mucositis following
chemoradiotherapy in patients with head-and-neck cancer. Int J Radiat Oncol Biol
Phys 65:1330-1337, 2006 Crossref, Medline, Google Scholar179. Lopez-Vaquero D,
Gutierrez-Bayard L, Rodriguez-Ruiz JA, et al: Double-blind randomized study of
oral glutamine on the management of radio/chemotherapy-induced mucositis and
dermatitis in head and neck cancer. Mol Clin Oncol 6:931-936, 2017 Crossref,
Medline, Google Scholar180. Pathak S, Soni TP, Sharma LM, et al: A randomized
controlled trial to evaluate the role and efficacy of oral glutamine in the
treatment of chemo-radiotherapy-induced oral mucositis and dysphagia in patients
with oropharynx and larynx carcinoma. Cureus 11:e4855, 2019 Medline, Google
Scholar181. Nihei S, Sato J, Komatsu H, et al: The efficacy of sodium azulene
sulfonate L-glutamine for managing chemotherapy-induced oral mucositis in cancer
patients: A prospective comparative study. J Pharm Health Care Sci 4:20, 2018
Crossref, Medline, Google Scholar182. Decker-Baumann C, Buhl K, Frohmüller S, et
al: Reduction of chemotherapy-induced side-effects by parenteral glutamine
supplementation in patients with metastatic colorectal cancer. Eur J Cancer
35:202-207, 1999 Crossref, Medline, Google Scholar183. Sarumathy S, Ismail AM,
Amirthalingam P: Efficacy and safety of oral glutamine in radiation induced oral
mucositis in patients with head and neck cancer. Asian J Pharm Clin Res
5:138-140, 2012 Google Scholar184. Diwan A, Khan S: Assessing role of oral
glutamine supplementation in radiation induced oral mucositis in head and neck
cancers. Ann Int Med Dental Res 4, 2018 Crossref, Google Scholar185. Okuno SH,
Woodhouse CO, Loprinzi CL, et al: Phase III controlled evaluation of glutamine
for decreasing stomatitis in patients receiving fluorouracil (5-FU)-based
chemotherapy. Am J Clin Oncol 22:258-261, 1999 Crossref, Medline, Google
Scholar186. Wang WS, Lin JK, Lin TC, et al: Oral glutamine is effective for
preventing oxaliplatin-induced neuropathy in colorectal cancer patients.
Oncologist 12:312-319, 2007 Crossref, Medline, Google Scholar187. Loven D,
Levavi H, Sabach G, et al: Long-term glutamate supplementation failed to protect
against peripheral neurotoxicity of paclitaxel. Eur J Cancer Care (Engl)
18:78-83, 2009 Crossref, Medline, Google Scholar188. Shah S, Rath H, Sharma G,
et al: Effectiveness of curcumin mouthwash on radiation-induced oral mucositis
among head and neck cancer patients: A triple-blind, pilot randomised controlled
trial. Indian J Dent Res 31:718-727, 2020 Crossref, Medline, Google Scholar189.
Delavarian Z, Pakfetrat A, Ghazi A, et al: Oral administration of nanomicelle
curcumin in the prevention of radiotherapy-induced mucositis in head and neck
cancers. Spec Care Dentist 39:166-172, 2019 Crossref, Medline, Google
Scholar190. Rao S, Dinkar C, Vaishnav LK, et al: The Indian spice turmeric
delays and mitigates radiation-induced oral mucositis in patients undergoing
treatment for head and neck cancer: An investigational study. Integr Cancer Ther
13:201-210, 2014 Crossref, Medline, Google Scholar191. Lustberg MB, Orchard TS,
Reinbolt R, et al: Randomized placebo-controlled pilot trial of omega 3 fatty
acids for prevention of aromatase inhibitor-induced musculoskeletal pain. Breast
Cancer Res Treat 167:709-718, 2018 Crossref, Medline, Google Scholar192.
Hershman DL, Unger JM, Crew KD, et al: Randomized multicenter placebo-controlled
trial of omega-3 fatty acids for the control of aromatase inhibitor–induced
musculoskeletal pain: SWOG S0927. J Clin Oncol 33:1910-1917, 2015 Link, Google
Scholar193. Martínez N, Herrera M, Frías L, et al: A combination of
hydroxytyrosol, omega-3 fatty acids and curcumin improves pain and inflammation
among early stage breast cancer patients receiving adjuvant hormonal therapy:
Results of a pilot study. Clin Translational Oncol 21:489-498, 2019 Crossref,
Medline, Google Scholar194. Ghoreishi Z, Esfahani A, Djazayeri A, et al: Omega-3
fatty acids are protective against paclitaxel-induced peripheral neuropathy: A
randomized double-blind placebo controlled trial. BMC Cancer 12:355, 2012
Crossref, Medline, Google Scholar195. Ebert N, Kensche A, Löck S, et al: Results
of a randomized controlled phase III trial: Efficacy of polyphenol-containing
cystus® tea mouthwash solution for the reduction of mucositis in head and neck
cancer patients undergoing external beam radiotherapy. Strahlenther Onkol
197:63-73, 2021 Crossref, Medline, Google Scholar196. Mutluay Yayla E, Izgu N,
Ozdemir L, et al: Sage tea-thyme-peppermint hydrosol oral rinse reduces
chemotherapy-induced oral mucositis: A randomized controlled pilot study.
Complement Ther Med 27:58-64, 2016 Crossref, Medline, Google Scholar197.
Aghamohammadi A, Moslemi D, Akbari J, et al: The effectiveness of Zataria
extract mouthwash for the management of radiation-induced oral mucositis in
patients: A randomized placebo-controlled double-blind study. Clin Oral Investig
22:2263-2272, 2018 Crossref, Medline, Google Scholar198. Ardakani MT, Ghassemi
S, Mehdizadeh M, et al: Evaluating the effect of Matricaria recutita and Mentha
piperita herbal mouthwash on management of oral mucositis in patients undergoing
hematopoietic stem cell transplantation: A randomized, double blind, placebo
controlled clinical trial. Complement Ther Med 29:29-34, 2016 Crossref,
Medline, Google Scholar199. Miranzadeh S, Adib-Hajbaghery M, Soleymanpoor L, et
al: Effect of adding the herb Achillea millefolium on mouthwash on chemotherapy
induced oral mucositis in cancer patients: A double-blind randomized controlled
trial. Eur J Oncol Nurs 19:207-213, 2015 Crossref, Medline, Google Scholar200.
Sahebjamee M, Mansourian A, Hajimirzamohammad M, et al: Comparative efficacy of
aloe vera and benzydamine mouthwashes on radiation-induced oral mucositis: A
triple-blind, randomised, controlled clinical trial. Oral Health Prev Dent
13:309-315, 2015 Medline, Google Scholar201. Erdem O, Gungormus Z: The effect of
royal jelly on oral mucositis in patients undergoing radiotherapy and
chemotherapy. Holist Nurs Pract 28:242-246, 2014 Crossref, Medline, Google
Scholar202. Sattari A, Shariati A, Shakiba Maram N, et al: Comparative study of
the effect of licorice root extract mouthwash and combined mouthwash on the
incidence and severity of chemotherapy-induced mucositis symptoms in colon
cancer patients admitted to intensive care units. Jundishapur J Chronic Dis Care
8:e88641, 2019 Crossref, Google Scholar203. Peng N, Yu M, Yang G, et al: Effects
of the Chinese medicine Yi Shen Jian Gu granules on aromatase
inhibitor-associated musculoskeletal symptoms: A randomized, controlled clinical
trial. Breast 37:18-27, 2018 Crossref, Medline, Google Scholar204. Chan A, De
Boer R, Gan A, et al: Randomized phase II placebo-controlled study to evaluate
the efficacy of topical pure emu oil for joint pain related to adjuvant
aromatase inhibitor use in postmenopausal women with early breast cancer: JUST
(Joints Under Study). Support Care Cancer 25:3785-3791, 2017 Crossref,
Medline, Google Scholar205. Niravath P, Hilsenbeck SG, Wang T, et al: Randomized
controlled trial of high-dose versus standard-dose vitamin D3 for prevention of
aromatase inhibitor-induced arthralgia. Breast Cancer Res Treat 177:427-435,
2019 Crossref, Medline, Google Scholar206. Cong Y, Sun K, He X, et al: A
traditional Chinese medicine Xiao-Ai-Tong suppresses pain through modulation of
cytokines and prevents adverse reactions of morphine treatment in bone cancer
pain patients. Mediators Inflamm 2015:961635, 2015 Crossref, Medline, Google
Scholar207. Bao YJ, Hua BJ, Hou W, et al: Alleviation of cancerous pain by
external compress with Xiaozheng Zhitong Paste. Chin J Integr Med 16:309-314,
2010 Crossref, Medline, Google Scholar208. Sun DZ, Jiao JP, Zhang X, et al:
Therapeutic effect of Jinlongshe Granule () on quality of life of stage IV
gastric cancer patients using EORTC QLQ-C30: A double-blind placebo-controlled
clinical trial. Chin J Integr Med 21:579-586, 2015 Crossref, Medline, Google
Scholar209. Ye X, Lu D, Chen X, et al: A multicenter, randomized, double-blind,
placebo-controlled trial of Shuangbai San for treating primary liver cancer
patients with cancer pain. J Pain Symptom Manage 51:979-986, 2016 Crossref,
Medline, Google Scholar210. Argyriou AA, Chroni E, Koutras A, et al: Preventing
paclitaxel-induced peripheral neuropathy: A phase II trial of vitamin E
supplementation. J Pain Symptom Manage 32:237-244, 2006 Crossref,
Medline, Google Scholar211. Wang C, Wang P, Ouyang H, et al: Efficacy of
traditional Chinese medicine in treatment and prophylaxis of radiation-induced
oral mucositis in patients receiving radiotherapy: A randomized controlled
trial. Integr Cancer Ther 17:444-450, 2018 Crossref, Medline, Google Scholar212.
Matsuda C, Munemoto Y, Mishima H, et al: Double-blind, placebo-controlled,
randomized phase II study of TJ-14 (Hangeshashinto) for infusional
fluorinated-pyrimidine-based colorectal cancer chemotherapy-induced oral
mucositis. Cancer Chemother Pharmacol 76:97-103, 2015 Crossref, Medline, Google
Scholar213. Naidu MU, Ramana GV, Ratnam SV, et al: A randomised, double-blind,
parallel, placebo-controlled study to evaluate the efficacy of MF 5232
(Mucotrol), a concentrated oral gel wafer, in the treatment of oral mucositis.
Drugs R D 6:291-298, 2005 Crossref, Medline, Google Scholar214. Putwatana P,
Sanmanowong P, Oonprasertpong L, et al: Relief of radiation-induced oral
mucositis in head and neck cancer. Cancer Nurs 32:82-87, 2009 Crossref,
Medline, Google Scholar215. You WC, Hsieh CC, Huang JT: Effect of extracts from
indigowood root (Isatis indigotica Fort.) on immune responses in
radiation-induced mucositis. J Altern Complement Med 15:771-778, 2009 Crossref,
Medline, Google Scholar216. Cabrera-Jaime S, Martínez C, Ferro-García T, et al:
Efficacy of Plantago major, chlorhexidine 0.12% and sodium bicarbonate 5%
solution in the treatment of oral mucositis in cancer patients with solid
tumour: A feasibility randomised triple-blind phase III clinical trial. Eur J
Oncol Nurs 32:40-47, 2018 Crossref, Medline, Google Scholar217. Demir Doğan M,
Can G, Meral R: Effectiveness of black mulberry molasses in prevention of
radiotherapy-induced oral mucositis: A randomized controlled study in head and
neck cancer patients. J Altern Complement Med 23:971-979, 2017 Crossref,
Medline, Google Scholar218. Luo Y, Feng M, Fan Z, et al: Effect of Kangfuxin
solution on chemo/radiotherapy-induced mucositis in nasopharyngeal carcinoma
patients: A multicenter, prospective randomized phase III clinical study. Evid
Based Complement Alternat Med 2016:8692343, 2016 Crossref, Medline, Google
Scholar219. Mansourian A, Amanlou M, Shirazian S, et al: The effect of “Curcuma
Longa” topical gel on radiation-induced oral mucositis in patients with head and
neck cancer. Int J Radiat Res 13:269-274, 2015 Google Scholar220. Chaitanya N,
Badam R, Aryasri AS, et al: Efficacy of improvised topical zinc (1%) ora-base on
oral mucositis during cancer chemo-radiation—A randomized study. J Nutr Sci
Vitaminol (Tokyo) 66:93-97, 2020 Crossref, Medline, Google Scholar221.
Heydarirad G, Cramer H, Choopani R, et al: Topical Costus sp. preparation as
palliative care for chemotherapy-induced peripheral neuropathy of patients: A
randomized placebo-controlled pilot trial. J Altern Complement Med 26:807-812,
2020 Crossref, Medline, Google Scholar222. Motoo Y, Tomita Y, Fujita H:
Prophylactic efficacy of ninjin'yoeito for oxaliplatin-induced cumulative
peripheral neuropathy in patients with colorectal cancer receiving postoperative
adjuvant chemotherapy: A randomized, open-label, phase 2 trial (HOPE-2). Int J
Clin Oncol 25:1123-1129, 2020 Crossref, Medline, Google Scholar223. Vitale MG,
Barbato C, Crispo A, et al: ZeOxaNMulti trial: A randomized, double-blinded,
placebo-controlled trial of oral PMA-zeolite to prevent chemotherapy-induced
side effects, in particular, peripheral neuropathy. Molecules 25:2297, 2020
Crossref, Google Scholar224. Bigdeli Shamloo MB, Nasiri M, Maneiy M, et al:
Effects of topical sesame (Sesamum indicum) oil on the pain severity of
chemotherapy-induced phlebitis in patients with colorectal cancer: A randomized
controlled trial. Complement Ther Clin Pract 35:78-85, 2019 Crossref,
Medline, Google Scholar225. Zhao C, Chen J, Yu B, et al: Effect of modified
taohongsiwu decoction on patients with chemotherapy-induced hand-foot syndrome.
J Tradit Chin Med 34:10-14, 2014 Crossref, Medline, Google Scholar226. Khurana
H, Pandey RK, Saksena AK, et al: An evaluation of Vitamin E and Pycnogenol in
children suffering from oral mucositis during cancer chemotherapy. Oral Dis
19:456-464, 2013 Crossref, Medline, Google Scholar227. Rezaeipour N, Jafari F,
Rezaeizadeh H, et al: Efficacy of a Persian medicine herbal compound (alcea
digitata alef and malva sylvestris L.) on prevention of radiation induced acute
mucositis in patients with head and neck cancer: A pilot study. Int J Cancer
Manag 10, 2017 Crossref, Medline, Google Scholar228. Ghalayani P, Emami H,
Pakravan F, et al: Comparison of triamcinolone acetonide mucoadhesive film with
licorice mucoadhesive film on radiotherapy-induced oral mucositis: A randomized
double-blinded clinical trial. Asia Pac J Clin Oncol 13:e48-e56, 2017 Crossref,
Medline, Google Scholar229. Zheng B, Zhu X, Liu M, et al: Randomized,
double-blind, placebo-controlled trial of shuanghua baihe tablets to prevent
oral mucositis in patients with nasopharyngeal cancer undergoing chemoradiation
therapy. Int J Radiat Oncol Biol Phys 100:418-426, 2018 Crossref,
Medline, Google Scholar230. Rastelli AL, Taylor ME, Gao F, et al: Vitamin D and
aromatase inhibitor-induced musculoskeletal symptoms (AIMSS): A phase II,
double-blind, placebo-controlled, randomized trial. Breast Cancer Res Treat
129:107-116, 2011 Crossref, Medline, Google Scholar231. Shapiro AC, Adlis SA,
Robien K, et al: Randomized, blinded trial of vitamin D3 for treating aromatase
inhibitor-associated musculoskeletal symptoms (AIMSS). Breast Cancer Res Treat
155:501-512, 2016 Crossref, Medline, Google Scholar232. Kono T, Hata T, Morita
S, et al: Goshajinkigan oxaliplatin neurotoxicity evaluation (GONE): A phase 2,
multicenter, randomized, double-blind, placebo-controlled trial of goshajinkigan
to prevent oxaliplatin-induced neuropathy. Cancer Chemother Pharmacol
72:1283-1290, 2013 Crossref, Medline, Google Scholar233. Moriyama S, Hinode D,
Yoshioka M, et al: Impact of the use of Kampo medicine in patients with
esophageal cancer during chemotherapy: A clinical trial for oral hygiene and
oral condition. J Med Invest 65:184-190, 2018 Crossref, Medline, Google
Scholar234. Nishioka M, Shimada M, Kurita N, et al: The Kampo medicine,
Goshajinkigan, prevents neuropathy in patients treated by FOLFOX regimen. Int J
Clin Oncol 16:322-327, 2011 Crossref, Medline, Google Scholar235. Halm MA, Baker
C, Harshe V: Effect of an essential oil mixture on skin reactions in women
undergoing radiotherapy for breast cancer: A pilot study. J Holist Nurs
32:290-303, 2014 Crossref, Medline, Google Scholar236. Izgu N, Ozdemir L, Basal
FB: Effect of aromatherapy massage on chemotherapy-induced peripheral
neuropathic pain and fatigue in patients receiving oxaliplatin: An open label
quasi-randomized controlled pilot study. Cancer Nurs 42:139-147, 2019 Crossref,
Medline, Google Scholar237. Nekuzad N, Torab TA, Mojab F, et al: Effect of
external use of sesame oil in the prevention of chemotherapy-induced phlebitis.
Iran J Pharm Res 11:1065-1071, 2012 Medline, Google Scholar238. Yayla EM,
Ozdemir L: Effect of inhalation aromatherapy on procedural pain and anxiety
after needle insertion into an implantable central venous port catheter: A
quasi-randomized controlled pilot study. Cancer Nurs 42:35-41, 2019 Crossref,
Medline, Google Scholar239. Soden K, Vincent K, Craske S, et al: A randomized
controlled trial of aromatherapy massage in a hospice setting. Palliat Med
18:87-92, 2004 Crossref, Medline, Google Scholar240. Liossi C, Hatira P:
Clinical hypnosis versus cognitive behavioral training for pain management with
pediatric cancer patients undergoing bone marrow aspirations. Int J Clin Exp
Hypn 47:104-116, 1999 Crossref, Medline, Google Scholar241. Liossi C, Hatira P:
Clinical hypnosis in the alleviation of procedure-related pain in pediatric
oncology patients. Int J Clin Exp Hypn 51:4-28, 2003 Crossref, Medline, Google
Scholar242. Hawkins PJ, Liossi C, Ewart BW, et al: Hypnosis in the alleviation
of procedure related pain and distress in paediatric oncology patients. Contemp
Hypnosis 15:199-207, 1998 Crossref, Google Scholar243. Smith JT, Barabasz A,
Barabasz M: Comparison of hypnosis and distraction in severely 111 children
undergoing painful medical procedures, 1996 undergoing painful medical
procedures. J Couns Psychol 43:187-195, 1996 Crossref, Google Scholar244.
Pourmovahed Z, Dehghani K, Sherafat A: Effectiveness of regular breathing
technique (hey-hu) on reduction of intrathecal injection pain in leukemic
children: A randomized clinical trial. Iran J Pediatr 23:564-568, 2013
Medline, Google Scholar245. Nguyen TN, Nilsson S, Hellström AL, et al: Music
therapy to reduce pain and anxiety in children with cancer undergoing lumbar
puncture: A randomized clinical trial. J Pediatr Oncol Nurs 27:146-155, 2010
Crossref, Medline, Google Scholar246. Gershon J, Zimand E, Pickering M, et al: A
pilot and feasibility study of virtual reality as a distraction for children
with cancer. J Am Acad Child Adolesc Psychiatry 43:1243-1249, 2004 Crossref,
Medline, Google Scholar247. Gerçeker G, Bektaş M, Aydınok Y, et al: The effect
of virtual reality on pain, fear, and anxiety during access of a port with huber
needle in pediatric hematology-oncology patients: Randomized controlled trial.
Eur J Oncol Nurs 50:101886, 2021 Crossref, Medline, Google Scholar248. Oberbaum
M, Yaniv I, Ben-Gal Y, et al: A randomized, controlled clinical trial of the
homeopathic medication TRAUMEEL S in the treatment of chemotherapy-induced
stomatitis in children undergoing stem cell transplantation. Cancer 92:684-690,
2001 Crossref, Medline, Google Scholar249. Soares ADS, Wanzeler AMV, Cavalcante
GHS, et al: Therapeutic effects of andiroba (Carapa guianensis Aubl) oil,
compared to low power laser, on oral mucositis in children underwent
chemotherapy: A clinical study. J Ethnopharmacol 264:113365, 2021 Crossref,
Medline, Google Scholar250. Tomaževič T, Jazbec J: A double blind randomised
placebo controlled study of propolis (bee glue) effectiveness in the treatment
of severe oral mucositis in chemotherapy treated children. Complement Ther Med
21:306-312, 2013 Crossref, Medline, Google Scholar251. Pourdeghatkar F, Motaghi
M, Darbandi BT, et al: Comparative effect of chamomile mouthwash and topical
mouth rinse in prevention of chemotherapy-induced oral mucositis in Iranian
pediatric patients with acute lymphoblastic leukemia. Iran J Blood Cancer
9:84-88, 2017 Google Scholar252. Shea BJ, Reeves BC, Wells G, et al: AMSTAR 2: A
critical appraisal tool for systematic reviews that include randomised or
non-randomised studies of healthcare interventions, or both. BMJ 358:j4008, 2017
Crossref, Medline, Google Scholar253. Farrar JT, Young JP Jr, LaMoreaux L, et
al: Clinical importance of changes in chronic pain intensity measured on an
11-point numerical pain rating scale. Pain 94:149-158, 2001 Crossref,
Medline, Google Scholar254. Peppone LJ, Janelsins MC, Kamen C, et al: The effect
of YOCAS©® yoga for musculoskeletal symptoms among breast cancer survivors on
hormonal therapy. Breast Cancer Res Treat 150:597-604, 2015 Crossref,
Medline, Google Scholar255. Hershman DL, Shao T, Kushi LH, et al: Early
discontinuation and non-adherence to adjuvant hormonal therapy are associated
with increased mortality in women with breast cancer. Breast Cancer Res Treat
126:529-537, 2011 Crossref, Medline, Google Scholar256. Henry NL, Unger JM,
Schott AF, et al: Randomized, multicenter, placebo-controlled clinical trial of
duloxetine versus placebo for aromatase inhibitor–associated arthralgias in
early-stage breast cancer: SWOG S1202. J Clin Oncol 36:326-332, 2018
Link, Google Scholar257. Irwin ML, Cartmel B, Gross CP, et al: Randomized
exercise trial of aromatase inhibitor–induced arthralgia in breast cancer
survivors. J Clin Oncol 33:1104-1111, 2015 Link, Google Scholar258. Gupta A,
Henry NL, Loprinzi CL: Management of aromatase inhibitor-induced musculoskeletal
symptoms. JCO Oncol Pract 16:733-739, 2020 Link, Google Scholar259. Bao T, Zhi
I, Baser R, et al: Yoga for chemotherapy-induced peripheral neuropathy and fall
risk: A randomized controlled trial. JNCI Cancer Spectr 4:pkaa048, 2020
Crossref, Medline, Google Scholar260. Ge J, Fishman J, Vapiwala N, et al:
Patient-physician communication about complementary and alternative medicine in
a radiation oncology setting. Int J Radiat Oncol Biol Phys 85:e1-e6, 2013
Crossref, Medline, Google Scholar261. Lee RT, Barbo A, Lopez G, et al: National
survey of US oncologists' knowledge, attitudes, and practice patterns regarding
herb and supplement use by patients with cancer. J Clin Oncol 32:4095-4101, 2014
Link, Google Scholar262. Bao T, Li Q, DeRito JL, et al: Barriers to acupuncture
use among breast cancer survivors: A cross-sectional analysis. Integr Cancer
Ther 17:854-859, 2018 Crossref, Medline, Google Scholar263. Liou KT, Hung TKW,
Meghani SH, et al: What if acupuncture were covered by insurance for pain
management? A cross-sectional study of cancer patients at one academic center
and 11 community hospitals. Pain Med 20:2060-2068, 2019 Crossref,
Medline, Google Scholar264. Gilligan T, Coyle N, Frankel RM, et al:
Patient-clinician communication: American Society of Clinical Oncology consensus
guideline. J Clin Oncol 35:3618-3632, 2017 Link, Google Scholar265. Patel MI,
Lopez AM, Blackstock W, et al: Cancer disparities and health equity: A policy
statement from the American Society of Clinical Oncology. J Clin Oncol
38:3439-3448, 2020 Link, Google Scholar266. Kim ES, Bruinooge SS, Roberts S, et
al: Broadening eligibility criteria to make clinical trials more representative:
American Society of Clinical Oncology and Friends of Cancer Research Joint
Research statement. J Clin Oncol 35:3737-3744, 2017 Link, Google Scholar267.
Availability of integrative medicine therapies at National Cancer
Institute-designated comprehensive cancer centers and community hospitals. J
Altern Complement Med 27:1011-1013, 2021 Crossref, Medline, Google Scholar268.
Witt CM, Balneaves LG, Carlson LE, et al: Education competencies for integrative
oncology-results of a systematic review and an international and
interprofessional consensus procedure. J Cancer Educ 37:499-507, 2022 Crossref,
Medline, Google Scholar269. Zhi WI, Gentile D, Diller M, et al: Patient-reported
outcomes of pain and related symptoms in integrative oncology practice and
clinical research: Evidence and recommendations. Oncology (Williston Park)
35:35-41, 2021 Crossref, Medline, Google Scholar270. Nahin RL, Barnes PM,
Stussman BJ: Insurance coverage for complementary health approaches among adult
users: United States, 2002 and 2012. NCHS Data Brief:1-8, 2016 Medline, Google
Scholar271. Gordon LG, Merollini KMD, Lowe A, et al: A systematic review of
financial toxicity among cancer survivors: We can't pay the co-pay. Patient
10:295-309, 2017 Crossref, Medline, Google Scholar272. Ben-Arye E, Elly D,
Samuels N, et al: Effects of a patient-tailored integrative oncology
intervention in the relief of pain in palliative and supportive cancer care. J
Cancer Res Clin Oncol 147:2361-2372, 2021 Crossref, Medline, Google Scholar273.
Greenlee H, DuPont-Reyes MJ, Balneaves LG, et al: Clinical practice guidelines
on the evidence-based use of integrative therapies during and after breast
cancer treatment. CA Cancer J Clin 67:194-232, 2017 Crossref, Medline, Google
Scholar274. Deng GE, Rausch SM, Jones LW, et al: Complementary therapies and
integrative medicine in lung cancer: Diagnosis and management of lung cancer,
3rd ed: American College of Chest Physicians evidence-based clinical practice
guidelines. Chest 143:e420S-e436S, 2013 Crossref, Medline, Google Scholar275.
Deng G, Frenkel M, Cohen L, et al: Society for integrative oncology.
Evidence-based clinical practice guidelines for integrative oncology:
Complementary therapies and botanicals. Journal of the Society for Integrative
Oncology, 7, 85-120. J Soc Integr Oncol 7:85-120, 2009 Medline, Google
Scholar276. Lyman GH, Greenlee H, Bohlke K, et al: Integrative therapies during
and after breast cancer treatment: ASCO endorsement of the SIO clinical practice
guideline. J Clin Oncol 36:2647-2655, 2018 Link, Google Scholar





OPTIONS & TOOLS

Export Citation Track Citation Add To Favorites

 * Rights & Permissions

Facebook Twitter Email AddThis


Downloaded 5,394 times


ASCO GUIDELINES PODCAST




COMPANION ARTICLES

No companion articles


ARTICLE CITATION

DOI: 10.1200/JCO.22.01357 Journal of Clinical Oncology

Published online September 19, 2022.

PMID: 36122322


WE RECOMMEND

 1. Efficacy of Complementary and Alternative Medicine Therapies in Relieving
    Cancer Pain: A Systematic Review
    Aditya Bardia et al., J Clin Oncol, 2016
 2. Salivary Gland Hypofunction and/or Xerostomia Induced by Nonsurgical Cancer
    Therapies: ISOO/MASCC/ASCO Guideline
    Valeria Mercadante et al., J Clin Oncol, 2021
 3. Prevention and Management of Chemotherapy-Induced Peripheral Neuropathy in
    Survivors of Adult Cancers: ASCO Guideline Update
    Charles L. Loprinzi et al., J Clin Oncol, 2020
 4. Palliative Care and the Management of Common Distressing Symptoms in
    Advanced Cancer: Pain, Breathlessness, Nausea and Vomiting, and Fatigue
    Lesley A. Henson et al., J Clin Oncol, 2020
 5. Systematic Review on Electronic Health Interventions for Patients With
    Breast Cancer: Revisiting the Methodology
    Meng Lv et al., J Clin Oncol, 2022

 1. Laying to Rest Psychostimulants for Cancer-Related Fatigue?
    Kathryn J. Ruddy et al., J Clin Oncol, 2014
 2. Treating Cancer-Related Fatigue: The Search for Interventions That Target
    Those Most in Need
    Julienne E. Bower, J Clin Oncol, 2012
 3. Acupuncture Treatment for Cancer Pain and Chemotherapy-Induced Peripheral
    Neuropathy
    By Bahar Javdan et al., The ASCO Post, 2014
 4. Supportive Care: Low Cost, High Value
    Razvan Andrei Popescu et al., ASCO Ed Book, 2021
 5. Neoadjuvant Chemotherapy, Endocrine Therapy, and Targeted Therapy for Breast
    Cancer: ASCO Guideline
    Larissa A. Korde et al., J Clin Oncol, 2021

Powered by
 * Privacy policy
 * Do not sell my personal information
 * Google Analytics settings


I consent to the use of Google Analytics and related cookies across the TrendMD
network (widget, website, blog). Learn more
Yes No








QUICK LINKS


CONTENT

Newest Articles
Archive
Meeting Abstracts


JOURNAL INFORMATION

About
Editorial Roster
Contact Us
Permissions


RESOURCES

Authors
Reviewers
Subscribers
Institutions
Advertisers


SUBMIT YOUR MANUSCRIPT


SUBSCRIBE TO THIS JOURNAL


ASCO FAMILY OF SITES


JOURNALS

Journal of Clinical Oncology
JCO Oncology Practice
JCO Global Oncology
JCO Clinical Cancer Informatics
JCO Precision Oncology


PUBLICATIONS

ASCO Educational Book
ASCO Daily News
ASCO Connection
The ASCO Post



EDUCATION

ASCO eLearning
ASCO Meetings
Cancer.Net


OTHER SITES

ASCO.org
ASCO Author Services
ASCO Career Center
CancerLinQ
Conquer Cancer Foundation
TAPUR Study

 * 
   American Society of Clinical Oncology
 * 2318 Mill Road, Suite 800, Alexandria, VA 22314
 * © 2022 American Society of Clinical Oncology

Terms of Use | Privacy Policy | Cookies











This site uses tracking technologies through the use of permanent cookies and
web beacons/pixel tags. By default, cookies are set to “Allow all cookies.” If
you continue to use this site, then you acknowledge our use of cookies. For
additional information, including on how to change your cookie settings, please
visit “Cookies Settings” and review our Privacy Policy and Terms of Use.

Cookies Settings Accept Cookies



YOUR PRIVACY

ASCO is committed to transparency regarding our websites and the ways we process
data. When you visit our site, we may store or retrieve information on your
browser, mostly in the form of cookies. This information might be about you,
your preferences, your location, or your device and is mostly used to make the
site work as you expect it to and to personalize your web experience with us.

Because we respect your right to privacy, you can choose not to allow some or
all types of cookies. Click on the different category headings to find out more
about the types of cookies used on our websites and change your default settings
to match your preferences. Please read these carefully. Blocking some types of
cookies may impact your experience on the site, including our ability to
personalize the content you receive from us.

For a full explanation of the personal and non-personal information we collect
on our site, including how we use that information and your rights regarding
that information, please review our Privacy Policy. Use of our website is also
subject to our Terms of Use.
Allow All


MANAGE CONSENT PREFERENCES

ESSENTIAL WEBSITE COOKIES

Always Active

These cookies are necessary for the website to function and are sometimes
referred to as “strictly necessary” cookies. They make sure the website delivers
you information and services in an optimal way.

They are often set in response to an action you take, such as changing your
cookie preferences, setting your privacy preferences, logging in to our website,
asking the site to remember you on subsequent pages, or filling in forms. These
cookies do not identify you personally.

You can set your browser to block or alert you about all cookies, including
essential website cookies, but some parts of the site will not work as a result.



Cookies Details‎

PERFORMANCE AND FUNCTIONALITY COOKIES

Performance and Functionality Cookies

These cookies enhance the performance and functionality of our websites and the
services we provide. For example, these cookies can keep track of your visitor
session in between visits, enable you to share content through social media, use
embedded media players, and use comment features. They also help us balance
website load and improve site speed and performance.

All information these cookies collect is aggregated and therefore anonymous.
These cookies may be set by us or by third party providers whose services we
have added to our websites. These cookies are non-essential, but without these
cookies, certain functionality or enhanced features may become unavailable.



Cookies Details‎

PERSONALIZATION AND ANALYTICS COOKIES

Personalization and Analytics Cookies

These cookies collect information that is used to help us understand how our
websites and content are used, help us customize our websites and application
for you in order to enhance your experience, and help us improve the content
that ASCO creates to better meet our members’ and visitors’ needs. Examples
include cookies that show us which content might be most popular with our
visitors, understand browsing history of our users, understand the effectiveness
of our own advertising, and enable us to recommend content to individual users
based on their profile and activities on the website.

These cookies may be set by us or by third party providers whose services we
have added to our websites.

These cookies are non-essential to the functionality of the site and may contain
information that enables us or our third party providers to identify you and
build a profile of your interests. Without these cookies, you will not be able
to have a customized or personalized experience within our website.



Cookies Details‎

ADVERTISING COOKIES AND SOCIAL MEDIA COOKIES

Advertising Cookies and Social Media Cookies

Advertising (or Targeting) cookies are third party cookies that may be set
through our site by our advertising partners. They may be used by those
companies to build a profile of your interests and show you relevant ads on
other sites.

Social Media Cookies are cookies set by a range of social media services that we
have added to the site to enable you to share our content with your friends and
networks. They are capable of tracking your activities across other sites and
building a profile of your interests. This may impact the content and messages
you see on other websites you visit.

These cookies and the data collected by the third parties may be combined with
data from other users or data about your activity on other sites. While the data
collected on our site is aggregate or non-personal, the data may be used by such
third parties to link you on other platforms or otherwise identify you.

If you do not allow these cookies, you may experience less targeted advertising.



Cookies Details‎
Back Button


PERFORMANCE COOKIES



Search Icon
Filter Icon

Clear
checkbox label label
Apply Cancel
Consent Leg.Interest
checkbox label label
checkbox label label
checkbox label label

 * 
   
   View Cookies
   
    * Name
      cookie name

Save Settings


Picked up by 5 news outlets
Blogged by 2
Tweeted by 99
On 4 Facebook pages
See more details
Picked up by 5 news outlets
Blogged by 2
Tweeted by 99
On 4 Facebook pages
See more details