Prevalence of and factors associated with treatment modification at first cycle in older adults with advanced cancer receiving palliative treatment.


Journal

Journal of geriatric oncology
ISSN: 1879-4076
Titre abrégé: J Geriatr Oncol
Pays: Netherlands
ID NLM: 101534770

Informations de publication

Date de publication:
11 2021
Historique:
received: 18 03 2021
revised: 09 06 2021
accepted: 18 06 2021
pubmed: 18 7 2021
medline: 15 12 2021
entrez: 17 7 2021
Statut: ppublish

Résumé

Treatment toxicities are common in older adults with cancer and consequently, treatment modifications are sometimes considered. We evaluated the prevalence and factors associated with treatment modifications at the first cycle in older patients receiving palliative systemic treatment. Patients (n = 369) from the GAP 70+ Trial (NCT02054741; PI: Mohile) usual care arm were included. Enrolled patients were aged 70+ with advanced cancer and ≥ 1 Geriatric Assessment (GA) domain impairment. Treatment modification was defined as any change from National Comprehensive Cancer Network guidelines or published clinical trials. Baseline variables included: 1) sociodemographic factors; 2) clinical variables; 3) GA domains; and 4) physician beliefs about life expectancy. Bivariate analyses and multivariable cluster-weighted generalized estimating equation model were conducted to assess the association of baseline variables with cycle 1 treatment modifications. Mean age was 77.2 years (range: 70-94); 62% had lung or gastrointestinal cancers, and 35% had treatment modifications at cycle 1. Increasing age by one year (odds ratio (OR) 1.1, 95% confidence interval [CI] 1.0-1.2), receipt of ≥second line of chemotherapy (OR 1.8, CI 1.1-3.0), functional impairment (OR 1.6, CI 1.1-2.3) and income ≤$50,000 (OR 1.7, CI 1.1-2.4) were independently associated with a higher likelihood of cycle 1 treatment modification. Treatment modifications occurred in 35% of older adults with advanced cancer at cycle 1. Increasing age, receipt of ≥second line of chemotherapy, functional impairment, and lower income were independently associated with treatment modifications. These findings emphasize the need for evidence-based regimens in older adults with cancer and GA impairments.

Identifiants

pubmed: 34272204
pii: S1879-4068(21)00142-9
doi: 10.1016/j.jgo.2021.06.007
pmc: PMC8557119
mid: NIHMS1728270
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT02054741']

Types de publication

Clinical Trial Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1208-1213

Subventions

Organisme : NCI NIH HHS
ID : R00 CA237744
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA233167
Pays : United States
Organisme : NIA NIH HHS
ID : R21 AG059206
Pays : United States
Organisme : NCI NIH HHS
ID : K99 CA237744
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189961
Pays : United States
Organisme : NIA NIH HHS
ID : R33 AG059206
Pays : United States
Organisme : NIA NIH HHS
ID : K24 AG056589
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA177592
Pays : United States
Organisme : NIA NIH HHS
ID : K76 AG064394
Pays : United States

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.

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Auteurs

Mostafa R Mohamed (MR)

James P Wilmot Cancer Institute, University of Rochester, New York, USA; Department of Public Health Sciences, University of Rochester, New York, USA.

Kaitlin Kyi (K)

Department of Medicine, University of Rochester, Rochester, New York, USA.

Supriya G Mohile (SG)

James P Wilmot Cancer Institute, University of Rochester, New York, USA.

Huiwen Xu (H)

Department of Surgery, Cancer Control, University of Rochester, New York, USA.

Eva Culakova (E)

Department of Surgery, Cancer Control, University of Rochester, New York, USA.

Kah Poh Loh (KP)

James P Wilmot Cancer Institute, University of Rochester, New York, USA.

Marie Flannery (M)

School of Nursing, University of Rochester, New York, USA.

Spencer Obrecht (S)

James P Wilmot Cancer Institute, University of Rochester, New York, USA.

Erika Ramsdale (E)

James P Wilmot Cancer Institute, University of Rochester, New York, USA.

Amita Patil (A)

James P Wilmot Cancer Institute, University of Rochester, New York, USA.

Richard F Dunne (RF)

James P Wilmot Cancer Institute, University of Rochester, New York, USA.

Grace DiGiovanni (G)

James P Wilmot Cancer Institute, University of Rochester, New York, USA.

Aram Hezel (A)

James P Wilmot Cancer Institute, University of Rochester, New York, USA.

Brian Burnette (B)

Cancer Research of Wisconsin and Northern Michigan, NCORP, USA.

Nisarg Desai (N)

Beebe Healthcare, Lewes, Delaware, NCORP, USA.

Jeffrey Giguere (J)

NCORP of the Carolinas, Prisma Health System, USA.

Allison Magnuson (A)

James P Wilmot Cancer Institute, University of Rochester, New York, USA. Electronic address: allison_magnuson@urmc.rochester.edu.

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