Patient perspectives on chemotherapy de-escalation in breast cancer.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
05 2021
Historique:
revised: 17 03 2021
received: 10 01 2021
accepted: 18 03 2021
pubmed: 2 5 2021
medline: 1 6 2021
entrez: 1 5 2021
Statut: ppublish

Résumé

Given excellent survival outcomes in breast cancer, there is interest in de-escalating the amount of chemotherapy delivered to patients. This approach may be of even greater importance in the setting of the COVID-19 pandemic. This concurrent mixed methods study included (1) interviews with patients and patient advocates and (2) a cross-sectional survey of women with breast cancer served by a charitable nonprofit organization. Questions evaluated interest in de-escalation trial participation, perceived barriers/facilitators to participation, and language describing de-escalation. Sixteen patient advocates and 24 patients were interviewed. Key barriers to de-escalation included fear of recurrence, worry about decision regret, lack of clinical trial interest, and dislike for focus on less treatment. Facilitators included trust in physician recommendation, toxicity avoidance, monitoring for progression, perception of good prognosis, and impact on daily life. Participants reported that the COVID-19 pandemic made them more likely to avoid chemotherapy if possible. Of 91 survey respondents, many (43%) patients would have been unwilling to participation in a de-escalation clinical trial. The most commonly reported barrier to participation was fear of recurrence (85%). Few patients (19%) considered clinical trials themselves as a barrier to de-escalation trial participation. The most popular terminology describing chemotherapy de-escalation was "lowest effective chemotherapy dose" (53%); no patients preferred the term "de-escalation." Fear of recurrence is a common concern among breast cancer survivors and patient advocates, contributing to resistance to de-escalation clinical trial participation. Additional research is needed to understand how to engage patients in de-escalation trials.

Sections du résumé

BACKGROUND
Given excellent survival outcomes in breast cancer, there is interest in de-escalating the amount of chemotherapy delivered to patients. This approach may be of even greater importance in the setting of the COVID-19 pandemic.
METHODS
This concurrent mixed methods study included (1) interviews with patients and patient advocates and (2) a cross-sectional survey of women with breast cancer served by a charitable nonprofit organization. Questions evaluated interest in de-escalation trial participation, perceived barriers/facilitators to participation, and language describing de-escalation.
RESULTS
Sixteen patient advocates and 24 patients were interviewed. Key barriers to de-escalation included fear of recurrence, worry about decision regret, lack of clinical trial interest, and dislike for focus on less treatment. Facilitators included trust in physician recommendation, toxicity avoidance, monitoring for progression, perception of good prognosis, and impact on daily life. Participants reported that the COVID-19 pandemic made them more likely to avoid chemotherapy if possible. Of 91 survey respondents, many (43%) patients would have been unwilling to participation in a de-escalation clinical trial. The most commonly reported barrier to participation was fear of recurrence (85%). Few patients (19%) considered clinical trials themselves as a barrier to de-escalation trial participation. The most popular terminology describing chemotherapy de-escalation was "lowest effective chemotherapy dose" (53%); no patients preferred the term "de-escalation."
CONCLUSIONS
Fear of recurrence is a common concern among breast cancer survivors and patient advocates, contributing to resistance to de-escalation clinical trial participation. Additional research is needed to understand how to engage patients in de-escalation trials.

Identifiants

pubmed: 33932097
doi: 10.1002/cam4.3891
pmc: PMC8124110
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3288-3298

Subventions

Organisme : Qualitative and Patient-Reported Outcomes Developing Shared Resource of the Wake Forest Baptist Comprehensive Cancer Center's NCI Cancer Center
ID : P30CA012197
Organisme : NCI NIH HHS
ID : P30 CA012197
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001420
Pays : United States
Organisme : ECOG-ACRIN Cancer Research Group
ID : 2UG1CA189828-06
Organisme : Wake Forest Clinical and Translational Science Institute's NCATS
ID : UL1TR001420
Organisme : American Cancer Society Mentored Research
ID : MRSG-17-051-01-PCSM
Organisme : Breast Cancer Research Foundation
Organisme : NCI NIH HHS
ID : UG1 CA189828
Pays : United States

Informations de copyright

© 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Gabrielle B Rocque (GB)

O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA.
Division of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
Department of Medicine, Division of Geriatrics, Gerontology, and Palliative Care, University of Alabama at Birmingham, Birmingham, AL, USA.

Courtney P Williams (CP)

Division of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.

Courtney Andrews (C)

UAB College of Arts and Sciences, School of Anthropology, University of Alabama at Birmingham, Birmingham, AL, USA.

Timothy C Childers (TC)

Division of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.

Kimberly D Wiseman (KD)

Wake Forest School of Medicine, Winston-Salem, NC, USA.

Kathleen Gallagher (K)

Patient Advocate Foundation, Hampton, VA, USA.

Nadine Tung (N)

Beth Israel Deaconess Medical Center, Boston, MA, USA.

Alan Balch (A)

Patient Advocate Foundation, Hampton, VA, USA.

Valerie M Lawhon (VM)

Division of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.

Stacey A Ingram (SA)

Division of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.

Thelma Brown (T)

O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA.

Tara Kaufmann (T)

Dell Medical School, University of Texas at Austin LiveSTRONG Cancer Institute, Austin, TX, USA.

Mary L Smith (ML)

ECOG-ACRIN Cancer Research Advocates Committee, Philadelphia, PA, USA.

Angela DeMichele (A)

Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA, USA.

Antonio C Wolff (AC)

John Hopkins University, Baltimore, MD, USA.

Lynne Wagner (L)

Wake Forest School of Medicine, Winston-Salem, NC, USA.

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Classifications MeSH