# Clinical impact of first-line chemotherapy combined with immune checkpoint inhibitors for limited-stage small cell lung cancer patients: a real-world propensity score matching study

**Authors:** Quanman Hu, Chenyi Zhou, Fei Zhao, Xiaoru Song, Yuan Ding, Xiyin Wang, Boying Wu, Huina Wang, Shuaiyin Chen, Bin Jia

PMC · DOI: 10.3389/fimmu.2026.1731123 · Frontiers in Immunology · 2026-01-21

## TL;DR

Adding immune checkpoint inhibitors to chemotherapy improves survival in limited-stage small cell lung cancer patients in real-world settings.

## Contribution

This study confirms the ADRIATIC trial results in real-world clinical practice using propensity score matching.

## Key findings

- Chemotherapy + ICIs group had significantly better overall survival (26.38 months) than chemotherapy alone (20.34 months).
- Chemotherapy + ICIs also showed improved progression-free survival (10.37 months vs 7.87 months).
- Radiotherapy, SII > 666.29, and PLR > 261.39 were independent prognostic factors for overall survival.

## Abstract

Findings from the ADRIATIC clinical trial revealed that adjuvant treatment with durvalumab following chemoradiotherapy (CRT) in limited-stage small cell lung cancer (LS-SCLC) significantly improved both overall survival (OS) and progression-free survival (PFS). However, the clinical impact remains uncertain in real-world clinical practice.

We gathered data of LS-SCLC patients at the First Affiliated Hospital of Zhengzhou University and conducted propensity score-matched analysis (PSM), Kaplan-Meier (K-M) method and Cox proportional hazards regression.

Prior to PSM, survival results demonstrated the mOS of the chemotherapy group was 20.34 months (95% confidence interval (CI): 18.80 - 23.57 months), whereas that of the chemotherapy + ICIs group was 26.38 months (95% CI: 22.97 - 38.90 months); the hazard ratio (HR) was 0.603 (95% CI: 0.413 - 0.880, P = 0.008, sample size: 102 vs 66). Simultaneously, the mPFS of the chemotherapy + ICIs group was also greater than that of the chemotherapy group, being 10.37 months (95% CI: 9.03 - 12.90 months) and 7.87 months (6.63 - 9.73 months), HR = 0.651 (95% CI: 0.457 - 0.927). After 1:1 matching for basic variables in the chemotherapy group (sample size: 66), its mOS was at 20.22 months, and mPFS was longer at 8.50 months. The multivariate analysis presented that radiotherapy, systemic immune-inflammation index (SII) > 666.29, and platelet-to-lymphocyte ratio (PLR) > 261.39 were independent prognostic factors for OS.

These results offer reliable references for clinicians when formulating treatment strategies for LS-SCLC patients and also provide support for future clinical trials.

## Linked entities

- **Diseases:** small cell lung cancer (MONDO:0008433)

## Full-text entities

- **Diseases:** inflammation (MESH:D007249), LS-SCLC (MESH:D055752)
- **Chemicals:** durvalumab (MESH:C000613593)
- **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/PMC12867874/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12867874/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12867874/full.md

---
Source: https://tomesphere.com/paper/PMC12867874