# Disparities in Non-Small Cell Lung Cancer (NSCLC) by Age, Sex, and Race: A Systematic Review and Meta-Analysis of Immune Checkpoint Inhibitor (ICI) Trials

**Authors:** Maxim Yaskolko, Christopher Liu, Alexander Barsouk, Jonathan H. Sussman, Adam A. Barsouk

PMC · DOI: 10.3390/cancers18010128 · Cancers · 2025-12-30

## TL;DR

This study finds Asian patients with lung cancer have better survival on immunotherapy than White patients, while Black patients are underrepresented in trials.

## Contribution

A meta-analysis of immunotherapy trials in NSCLC reveals survival disparities by race and highlights underrepresentation of Black patients.

## Key findings

- Asian patients had higher survival rates on immunotherapy compared to White patients.
- Black patients were underrepresented in the trials, limiting analysis of their outcomes.
- No significant differences in survival were found by sex or age.

## Abstract

We conducted a meta-analysis of all immunotherapy (PD-1, PD-L1, CTLA-4) trials in non-small cell lung cancer (NSCLC) for survival disparities by race, sex, and age. We found that Asian patients had higher rates of survival compared to White patients on immunotherapy and overall. Black patients were underrepresented in the trials. We did not find any difference in survival by sex or age. Furhter research and greater diversity in NSCLC trials is required to ensure optimal outcomes for all patient populations.

Background: While immune checkpoint inhibitors (ICIs) have improved survival in mNSCLC, outcomes may be disparate by age, race, and sex. However, given the limited diversity of trial populations, data are limited. Methods: A systematic review and meta-analysis were conducted of phase III prospective trials of ICIs in mNSCLC initiated after 2015, identified from PubMed and ClinicalTrials.gov in September 2025. Trials that did not report overall survival by race, sex, or age distribution were excluded. Random-effects meta-analyses were used to pool ratios of hazard ratios (RHRs) for overall survival to assess treatment-by-subgroup interactions by sex (men vs. women), race (white vs. Asian), and age (<65 vs. ≥65). Random-effects meta-analyses of odds ratios (ORs) for death were also performed for each subgroup in the investigational treatment arm and across all patients. Heterogeneity across trials was evaluated by Cochran’s Q test and I2 statistics. Publication bias was assessed by Egger’s tests and funnel plots. Results: A total of 21 trials comprising 10,950 patients were included in the meta-analysis. Women have a non-significantly smaller overall survival benefit with the investigational treatment than with control compared with men (RHR 0.91; p = 0.17). On investigational agents, white patients had higher odds of death (OR 1.76; p = 0.0496) compared to Asian patients. Similarly, white patients had higher odds of death across both treatment arms compared to Asian patients (OR 2.35; p < 0.001). No trials reported subgroup analysis for Black patients due to small sample sizes. Patients ≥65 years old have a non-significantly smaller overall survival benefit with investigational agents compared with control (RHR 0.92; p = 0.19). Discussion: This study did not identify significant differences in overall survival benefit on the investigational treatment across race, sex, or age subgroups. Still, it remains unclear whether women and patients ≥65 years old derive less survival benefit from ICIs than men and younger patients. Asian patients had significantly greater survival than white patients on investigational therapies and all therapies, while Black patients were underrepresented in trials. Our results highlight the need for more representative trial populations and standardized reporting of subgroup analysis to ensure equitable benefit and evaluation of ICIs in mNSCLC treatment. Our meta-analysis was limited by inconsistent data reporting across subgroups and by the lack of time-to-event survival data within subgroups.

## Linked entities

- **Diseases:** non-small cell lung cancer (MONDO:0005233), NSCLC (MONDO:0005233)

## Full-text entities

- **Diseases:** death (MESH:D003643), NSCLC (MESH:D002289)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12784937/full.md

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12784937/full.md

## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC12784937/full.md

---
Source: https://tomesphere.com/paper/PMC12784937