# Real-world study of adebrelimab as first-line therapy for extensive-stage small cell lung cancer: a retrospective study

**Authors:** Kaili Xu, Jian Wang, Zhenhe Weng, Junhui Wang, Jianxin Chen

PMC · DOI: 10.3389/fimmu.2025.1678020 · 2025-10-13

## TL;DR

A real-world study found that adebrelimab, combined with chemotherapy, improves survival in patients with extensive-stage small cell lung cancer, though with notable side effects.

## Contribution

This study provides real-world evidence supporting the efficacy and safety of adebrelimab in treating extensive-stage small cell lung cancer.

## Key findings

- Median overall survival was 15.0 months with adebrelimab-based therapy in real-world settings.
- ECOG PS ≥2, ≥2 metastatic organs, and elevated CRP predicted worse outcomes in patients.
- Hematologic toxicities and rare cardiotoxicity were observed in patients receiving adebrelimab.

## Abstract

Extensive-stage small cell lung cancer (ES-SCLC) has a poor prognosis, with historical median overall survival (OS) of 8–13 months under platinum-etoposide chemotherapy. While phase III trials established adebrelimab (anti-PD-L1) plus chemotherapy as a new standard, real-world evidence remains scarce. This study evaluated real-world efficacy, safety, and prognostic factors of first-line adebrelimab-based therapy.

In this retrospective study, thirty-five patients with ES-SCLC receiving adebrelimab as first-line treatment were analyzed. Endpoints included objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), OS, and adverse events (AEs). Prognostic factors were assessed via Cox regression.

Median age was 72 years; 88.6% were male, 85.7% had Eastern Cooperative Oncology Group Performance Status (ECOG PS) 0–1, and 51.4% had ≥2 metastatic sites. ORR was 62.8%, DCR 77.1%. Median PFS was 7.1 months (95% CI: 5.47–8.53), and median OS was 15.0 months (95% CI: 10.47–19.53). Multivariate analysis identified ECOG PS ≥2 as an independent predictor of inferior PFS (HR = 9.446, p=0.013), while ≥2 metastatic organs (HR = 3.594, p=0.046) and C-reactive Protein (CRP) ≥5 mg/L (HR = 3.337, p=0.044) predicted worse OS. Grade 3–4 AEs occurred in 74.3% of patients, primarily hematologic toxicities (neutropenia: 51.4%); two cases (5.7%) of myocarditis were observed.

Adebrelimab suggests potentially promising efficacy in ES-SCLC, aligning with pivotal trial data despite an older cohort. ECOG PS ≥2, high metastatic burden, and elevated CRP independently predict poorer outcomes. Vigilant monitoring for hematologic toxicity and rare cardiotoxicity is warranted.

## Linked entities

- **Proteins:** CD274 (CD274 molecule)
- **Diseases:** small cell lung cancer (MONDO:0008433), myocarditis (MONDO:0004496), neutropenia (MONDO:0001475)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}
- **Diseases:** ES-SCLC (MESH:D055752), myocarditis (MESH:D009205), cardiotoxicity (MESH:D066126), neutropenia (MESH:D009503), hematologic toxicities (MESH:D006402)
- **Chemicals:** Adebrelimab (-), platinum (MESH:D010984), etoposide (MESH:D005047)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12554772/full.md

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Source: https://tomesphere.com/paper/PMC12554772