Evidence map›Paper›PMID 42116962›Full record

ArticleCureus2026

Chemotherapy-Related Adverse Drug Reaction (ADR) Profile in Geriatric Cancer Patients: A Prospective Study From Western India.

Priyanka Srivastava, Nitiraj Shete, Barna Ganguly, Nirav N Asarawala

Abstract read
In one paragraph

Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Priyanka SrivastavaMedical Oncology, Rayos Comprehensive Cancer Care, Anand, IND.
Nitiraj SheteBiostatistics, Muljibhai Patel Urological Hospital, Nadiad, IND.
Barna GangulyPharmacology, Pramukhswami Medical College, Anand, IND.
Nirav N AsarawalaMedical Oncology, M.S. Patel Cancer Centre, Bhaikaka University, Anand, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Chemotherapy adverse drug reactions (ADRs) among geriatric cancer patients (≥65 years) are a major cause of morbidity. Real-world data for the Western Indian population are lacking. In the absence of data and guidelines, geriatric patients either suffer treatment-related toxicities or remain undertreated. The present study aimed to study the clinical profile, geriatric assessment (GA), chemotherapy-related ADRs, and survival outcomes. Methods This prospective, observational study enrolled patients aged ≥65 years who were starting curative-intent chemotherapy. Baseline clinical and GA was performed. Treatment details, including planned chemotherapy regimens and modifications in chemotherapy dosing, schedule, or protocol selection based on initial assessments, were recorded. Chemotherapy-related ADRs were assessed using the Common Terminology Criteria for Adverse Events version 5.0 (CTCAE v5.0). Grade 3-5 adverse events were defined as severe. In total, 150 patients were accrued. Patients were followed up for one year post-chemotherapy. Results Out of 150 patients, 72 patients (48%) completed all planned cycles. Forty-nine patients (32.66%) reported severe-grade ADRs (CTCAE grades 3, 4, and 5). A total of nine (6%) deaths were reported during chemotherapy (i.e., CTCAE grade 5). The baseline GA parameters were not associated with CTCAE grade (p value > 0.05, nonsignificant). The estimated Kaplan-Meier survival at the end of four years of follow-up suggests worse outcomes in patients who experienced severe-grade ADRs and were unable to complete all the planned chemotherapy cycles. Conclusions A significant proportion of geriatric cancer patients experience severe-grade chemotherapy ADRs. Completing planned chemotherapy cycles in patients being treated with curative intent is an important determinant of survival. Patients who experience severe-grade toxicities have adverse survival outcomes, emphasizing the need for personalized toxicity management.

Indexed as

adverse drug reactionschemotherapy dosegeriatric assessmentgeriatric oncologywestern indian population

Identifiers

PMID42116962
PMCPMC13157616

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