Evidence map›Paper›PMID 42497369›Full record

ArticleJCO oncology practice2026

Treatment Tolerability in Older Adults With Advanced Cancer Receiving Geriatric Assessment-Guided Versus Oncologist-Guided Primary Treatment Modification: Secondary Analysis of the GAP70+ Trial.

Mostafa R Mohamed, David Q Rich, Jennifer L Lund, Christopher L Seplaki, Marie Flannery, Riham Alieldin, Yingzhu Chen, Erika Ramsdale, Megan Wells, Allison Magnuson and 4 more

Registry-linked trialAbstract read
In one paragraph

Article in JCO oncology practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02054741 (A Geriatric Assessment Intervention for Patients Aged 70 and Over Receiving Chemotherapy or Similar Agents for Advanced Cancer), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02054741 nacompletednot on this map

A Geriatric Assessment Intervention for Patients Aged 70 and Over Receiving Chemotherapy or Similar Agents for Advanced Cancer: Reducing Toxicity in Older Adults

TypeinterventionalSponsorSupriya MohileRan2014 to 2021Enrolled733ConditionsAdult Solid Neoplasm, Toxicity, LymphomaArmsComprehensive Geriatric Assessment, Quality-of-Life Assessment, Survey Administration
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Mostafa R MohamedDepartment of Public Health, University of Rochester School of Medicine and Dentistry, Rochester, NY.ORCID 0000-0003-2936-5794
David Q RichDepartment of Public Health, University of Rochester School of Medicine and Dentistry, Rochester, NY.
Jennifer L LundDepartment of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC.ORCID 0000-0002-1108-0689
Christopher L SeplakiDepartment of Public Health, University of Rochester School of Medicine and Dentistry, Rochester, NY.ORCID 0000-0001-8296-7714
Marie FlanneryUniversity of Rochester School of Nursing, Rochester, NY.ORCID 0000-0003-2957-8482
Riham AlieldinDepartment of Surgery, University of Rochester School of Medicine and Dentistry, Rochester, NY.ORCID 0000-0001-7731-6298
Yingzhu ChenDepartment of Public Health, University of Rochester School of Medicine and Dentistry, Rochester, NY.ORCID 0009-0001-4672-9695
Erika RamsdaleDepartment of Public Health, University of Rochester School of Medicine and Dentistry, Rochester, NY.
Megan WellsJames P. Wilmot Cancer Institute, Division of Hematology/Oncology, Department of Medicine, University of Rochester, Rochester, NY.
Allison MagnusonJames P. Wilmot Cancer Institute, Division of Hematology/Oncology, Department of Medicine, University of Rochester, Rochester, NY.ORCID 0000-0002-0968-8265
Kah Poh LohJames P. Wilmot Cancer Institute, Division of Hematology/Oncology, Department of Medicine, University of Rochester, Rochester, NY.ORCID 0000-0002-6978-0418
Richard DunneJames P. Wilmot Cancer Institute, Division of Hematology/Oncology, Department of Medicine, University of Rochester, Rochester, NY.ORCID 0000-0001-6608-660X
Michelle JanelsinsDepartment of Surgery, University of Rochester School of Medicine and Dentistry, Rochester, NY.ORCID 0000-0003-2258-7247
Supriya MohileJames P. Wilmot Cancer Institute, Division of Hematology/Oncology, Department of Medicine, University of Rochester, Rochester, NY.ORCID 0000-0003-0867-327X

Funding

URCC NCORP Research BaseUG1CA189961 · NCI · UNIVERSITY OF ROCHESTER · PI Michelle C Janelsins, KAREN M. MUSTIAN · 2014 to 2026
$67.7M
Understanding Treatment Tolerability in Older Patients with CancerU01CA233167 · NCI · UNIVERSITY OF ROCHESTER · PI MOHILE, SUPRIYA G. · 2018 to 2023
$3.5M
A Patient-Oriented Research Program in Geriatric OncologyK24AG056589 · NIA · UNIVERSITY OF ROCHESTER · PI Supriya G. Mohile · 2018 to 2026
$1.5M
Decreasing Polypharmacy in Older Adults with Curable CancersK08CA248721 · NCI · UNIVERSITY OF ROCHESTER · PI RAMSDALE, ERIKA E · 2020 to 2024
$1.2M
NCI NIH HHS K08 CA248721NCI NIH HHS U01 CA233167NCI NIH HHS UG1 CA189961NIA NIH HHS K24 AG056589
6 · The paper itself

Abstract

purposePrimary treatment modification (PTM; changes in treatment dose or agents from standard guidelines) is common among older adults with advanced cancer because of aging-related vulnerabilities. Geriatric assessment evaluates aging-related factors to inform personalized treatment. We compared treatment tolerability between PTM guided by geriatric assessment-guided management (PTM-GAM) and PTM determined by usual oncologic care (PTM-UC).

methodsThis secondary analysis of the GAP70+ study (ClinicalTrials.gov identifier: NCT02054741; PI: Mohile) was restricted to patients age 70+ years with incurable solid tumors who initiated systemic therapy with a PTM (N=298). PTM-GAM (n = 169) was guided by GA results and management recommendations, whereas PTM-UC (n = 129) was based solely on oncologist evaluation. Tolerability outcomes within 3 months of treatment initiation included grade 3 to 5 toxicity, secondary dose reduction (any unplanned decrease in dose after treatment initiation), decline in activities of daily living (ADL), and unplanned hospitalization. Associations were evaluated using multivariable cluster-weighted generalized estimating equation models.

resultsThe mean age was 77 years, and GI cancers were most common (37%). Overall, 59% experienced ≥1 grade 3 to 5 toxicity. Compared with PTM-UC, PTM-GAM was associated with a lower risk of grade 3 to 5 toxicity (relative risk, 0.77 [95% CI, 0.65 to 0.91]). Secondary dose reductions occurred in 22% of patients, with lower risk in PTM-GAM (RR, 0.47 [95% CI, 0.30 to 0.72]). PTM-GAM was associated with a nonsignificant reduction in unplanned hospitalization (RR, 0.69 [95% CI, 0.45 to 1.03]). No difference was observed in ADL decline (RR, 1.04 [95% CI, 0.74 to 1.48]).

conclusionOlder adults with advanced cancer who received GA-guided PTM had a 23% lower risk of grade 3 to 5 toxicities and a 53% lower risk of secondary dose reduction compared with PTM based on usual oncologic care. These findings underscore the role of geriatric assessment in optimizing treatment decisions and improving tolerability.

Identifiers

PMID42497369
PMCPMC13488475

What Socratic holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.