RecruitingNCT07369596

Impact of Chemotherapy Dose Reductions on Survival Outcomes Among Older NSCLC Patients Without Actionable Mutations

Impact of Chemotherapy Dose Reductions on Survival Outcomes Among Older NSCLC Patients Without Actionable Mutations: A Retrospective Cohort Study.


Sponsor

University of Malaya

Enrollment

150 participants

Start Date

Jan 1, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

Evidence suggests that appropriately selected older adults can tolerate standard-dose chemotherapy and achieve survival outcomes comparable to younger patients. However, older adults are usually under-represented in clinical trials and often receive reduced doses of chemotherapy due to concerns regarding age-related frailty, polypharmacy, and toxicity. This study seeks to evaluate chemotherapy dosing patterns and associated survival outcomes in older patients.


Eligibility

Min Age: 65 Years

Inclusion Criteria4

  • Age ≥65 years
  • Histologically confirmed stage IV NSCLC
  • Negative for EGFR mutation, ALK rearrangement, and ROS1 fusion
  • Treated with at least ONE cycle of first-line chemotherapy

Exclusion Criteria2

  • Patients who received targeted therapy or immunotherapy as monotherapy in the first-line setting
  • Incomplete survival data

Interventions

OTHERProgression free survival

PFS

OTHEROverall survival

OS


Locations(4)

Queen Mary Hospital, The University of Hong Kong

Hong Kong, Hong Kong

Hospital Tengku Ampuan Afzan

Kuantan, Pahang, Malaysia

Hospital Wanita dan Kanak-Kanak Sabah

Kota Kinabalu, Sabah, Malaysia

Universiti Malaya Medical Centre

Kuala Lumpur, Malaysia

View Full Details on ClinicalTrials.gov

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NCT07369596


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