First-line camrelizumab plus chemotherapy followed by camrelizumab-apatinib maintenance for ES-SCLC: a single-arm phase II study.

Lung CancerSep 11, 2026 (epub)
Clinical ResearchOncology (Medical)

Minghui Zhang, Mingyuan Guo, Lijun Li et al.

✦ AI-curated · Sources linked

In 30 seconds

This single-arm phase II trial evaluated first-line camrelizumab plus platinum-etoposide followed by camrelizumab-apatinib maintenance in treatment-naïve patients with extensive-stage small-cell lung cancer. Among 41 enrolled patients, the 6-month progression-free survival rate was 71.1% (95% CI: 53.9-82.9) at a median follow-up of 31.0 months. Median progression-free and overall survival were 8.7 and 17.2 months, respectively. Grade ≥ 3 treatment-related adverse events occurred in 22.0% of patients, with no treatment-related deaths. Exploratory analyses linked clinical benefit with immune and gene-expression patterns.

Key findings

  • The 6-month PFS rate was 71.1% (95% CI: 53.9-82.9); median PFS was 8.7 months (95% CI: 6.9-10.6).
  • Median OS was 17.2 months (95% CI: 14.5-19.9); ORR was 82.9% and DCR was 92.7%.
  • Grade ≥ 3 treatment-related adverse events occurred in 22.0% of patients; no treatment-related deaths were reported.
  • Durable clinical benefit was associated with a high-CD8/low-M2 immune phenotype; an exploratory 9-gene pattern was associated with PFS.

Why it matters

The study provides preliminary evidence on a treatment sequence that adds antiangiogenic therapy during maintenance rather than induction for ES-SCLC. Its reported activity and safety outcomes may inform further evaluation of this approach, while the exploratory biomarker findings offer hypotheses for identifying patients more likely to benefit, not validated selection tools.

What to keep in mind

The study was single-arm and included 41 patients, so it cannot establish comparative benefit. The immune and gene-expression findings were exploratory.

Source

Published in Lung Cancer. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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