Clinical Trial

Prediction of Response to PD-L1 Inhibitor After Chemoradiotherapy in Limited-Stage Small-Cell Lung Cancer Using Multi-omics-based Liquid Biopsy

Recruiting
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Summary
This study aims to explore the efficacy and safety of immunotherapy (PD-L1 inhibitor) maintenance following high-dose hyperfractionated simultaneous integrated boost radiotherapy concurrent chemotherapy in patients with limited-stage small cell lung cancer (LS-SCLC). This study is a prospective observational study. Additionally, liquid biopsy technology will be employed to identify biomarkers that can predict the efficacy of PD-L1 inhibitor after chemoradiotherapy in LS-SCLC.
Trial Details
NCT Number NCT06869239
Lead Sponsor Peking University Cancer Hospital & Institute
Conditions Limited-stage Small Cell Lung Cancer (LS-SCLC)
Enrollment 65 participants
Start Date 2025-02-25
Primary Completion 2027-01-03 (estimated)
Study Completion 2028-01-03 (estimated)
Updated on ClinicalTrials.gov 2025-03-11