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Systematic review and meta-analysis shows immune checkpoint inhibitors improve survival in first-line ES-SCLC but not as single agents in second-line

Systematic review and meta-analysis shows immune checkpoint inhibitors improve survival in first-lin…
Photo by Trust "Tru" Katsande / Unsplash
Key Takeaway
Consider ICIs with chemotherapy for first-line ES-SCLC; avoid single-agent use in second-line.

This systematic review and meta-analysis examines the role of immune checkpoint inhibitors in patients with extensive stage small-cell lung cancer receiving first-line or second-line therapy. The analysis focused on overall survival, progression-free survival, objective response rate, and grade 3+ adverse events. The study population included patients treated with immune checkpoint inhibitors and chemotherapy compared to chemotherapy alone.

The pooled analysis demonstrated that immune checkpoint inhibitors decreased the risk of death by 19% with a hazard ratio of 0.81 and a 95% CI of 0.76-0.86. Progression-free survival improved with a hazard ratio of 0.78 and a 95% CI of 0.67-0.91, indicating a 22% decreased risk of disease progression. The objective response rate also improved with an odds ratio of 0.79 and a 95% CI of 0.66-0.95.

Safety data revealed that immune checkpoint inhibitors were associated with increased grade 3+ diarrhea, showing an odds ratio of 3.63 and a 95% CI of 1.46-9.02. The authors noted an acceptable safety profile in the first-line setting but highlighted that biomarkers predicting long-term benefit are needed to further improve outcomes. The review concludes that while efficacy benefits exist, ICIs should not be used in the second-line setting as single agents.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
OBJECTIVES: Despite a good response to first-line chemotherapy, small-cell lung cancer (SCLC) has high relapse rates and a poor prognosis. We conducted a systematic review and meta-analysis to assess the role of immune checkpoint inhibitors (ICIs) in the treatment of extended stage SCLC (ES-SCLC), in different lines of therapy. METHODS: Medline (PubMed), EMBASE, and Cochrane Library databases between January 2010 and March 2025 and conference proceedings between 2018 and 2025 were searched for RCTs assessing ICIs versus chemotherapy in patients with ES-SCLC. Primary endpoints were overall survival (OS) and progression-free survival (PFS). Secondary endpoints included objective response rate (ORR) and grade 3+ adverse events. Pooled hazard ratios (HR) for OS and PFS were meta-analyzed using the generic inverse variance method, and random-effect models were used to compute pooled estimates. Subgroup analyses compared survival by line of therapy, sex, age, and ECOG status. RESULTS: ICIs decreased risk of death by 19% (HR: 0.81, 95% CI: 0.76-0.86). OS benefit was regardless of age, sex, or ECOG, but only in first-line treatment. ICIs decreased the risk of disease progression by 22% (HR: 0.78, 95% CI: 0.67-0.91), with PFS benefit restricted to first-line treatment with a detrimental effect in the second line. ICIs improved ORR (OR: 0.79, 95% CI: 0.66-0.95), but were associated with increased grade 3+diarrhea (OR: 3.63, 95% CI: 1.46-9.02). CONCLUSIONS: ICIs conferred efficacy benefits and an acceptable safety profile in the treatment of patients with ES-SCLC in the first-line, but should not be used in the second-line as single agents. Biomarkers predicting long-term benefit are needed to further improve outcomes.
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