# Comparison of real-world efficacy and safety of nivolumab plus ipilimumab or pembrolizumab combined with platinum-based chemotherapy as first-line treatment for advanced non-small cell lung cancer in a German population

**Authors:** Moritz Weber, Alexander Freiherr von Hammerstein-Equord, Manuela Weinreich, Stefan Andreas, Achim Rittmeyer

PMC · DOI: 10.1007/s00262-025-04244-4 · Cancer Immunology, Immunotherapy : CII · 2026-01-31

## TL;DR

This study compares two treatment options for advanced lung cancer in Germany and finds similar effectiveness and safety.

## Contribution

A real-world comparison of nivolumab plus ipilimumab and pembrolizumab in treating advanced non-small cell lung cancer in Germany.

## Key findings

- Median overall survival and treatment duration were similar between the two treatment groups.
- NIC had more immune-related side effects, while PC had more chemotherapy-related side effects.
- No significant differences in serious adverse events or treatment-related deaths were observed.

## Abstract

In advanced non-small cell lung cancer (NSCLC), nivolumab plus ipilimumab with platinum-based chemotherapy (NIC) and pembrolizumab with platinum-based chemotherapy (PC) are commonly used treatment options. We conducted a single-center retrospective analysis comparing the two options under real-world conditions in Germany.

We collected data from patients whose treatment was initiated between July 2018 and June 2023. Primary endpoints were overall survival and safety. Categorical data were compared using the chi-squared test or Fisher’s exact test. Overall survival was compared using the Kaplan–Meier method and the log-rank test.

200 patients, 77 treated with NIC and 123 treated with PC, were included. Baseline characteristics were unbalanced with significantly more older, squamous, and PD-L1-negative cases in the NIC group. Median overall survival (OS) and time to treatment discontinuation (TTD) were not significantly different in the NIC and PC groups (13.6 vs. 14.1 months / 5.8 vs. 6.2 months). Clinically significant adverse events (AEsi), related treatment discontinuations, and treatment-related deaths also did not differ significantly (p = 0.885/p = 1.000/p = 0.709). There were more immune-related AEsi in the NIC group (p = 0.001) and more chemo-related AEsi in the PC group (p < 0.001).

NIC and PC seem to be equally supportable options in the treatment of advanced NSCLC. Further analyses are needed to validate our findings.

The online version contains supplementary material available at 10.1007/s00262-025-04244-4.

## Linked entities

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

## Full-text entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, STK11 (serine/threonine kinase 11) [NCBI Gene 6794] {aka LKB1, PJS, hLKB1}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, ROS1 (ROS proto-oncogene 1, receptor tyrosine kinase) [NCBI Gene 6098] {aka MCF3, ROS, c-ros-1}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, KEAP1 (kelch like ECH associated protein 1) [NCBI Gene 9817] {aka INrf2, KLHL19}, KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}
- **Diseases:** TRD (MESH:D016609), PC (MESH:D019292), emesis (MESH:D014839), Skin reactions (MESH:D012871), Lung cancer (MESH:D008175), hematological AEs (MESH:D006402), NSCLC (MESH:D002289), Solid Tumors (MESH:D009369), death (MESH:D003643), cytotoxicity (MESH:D064420), nausea (MESH:D009325), mucositis (MESH:D052016), bone metastases (MESH:D009362), pneumonitis (MESH:D011014)
- **Chemicals:** CheckMate-9LA (-), Carboplatin (MESH:D016190), platinum (MESH:D010984), PC (MESH:D017671), pembrolizumab (MESH:C582435), prednisolone (MESH:D011239), infliximab (MESH:D000069285), Pemetrexed (MESH:D000068437), cisplatin (MESH:D002945), NIC (MESH:D009538), ipilimumab (MESH:D000074324), paclitaxel (MESH:D017239), nivolumab (MESH:D000077594)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12860776/full.md

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Source: https://tomesphere.com/paper/PMC12860776