Precision Induction Therapy for Inoperable NSCLC in Stage III Disease: A Phase II Umbrella Clinical Trial
Release date:
2025-01-26
Description:
The objective is to assess the efficacy and safety of precision induction therapies in patients with unresectable stage III NSCLC selected based on tumor PD-L1 expression. Patients were stratified into groups receiving Sintilimab monotherapy, Sintilimab plus IBI305, or Sintilimab combined with chemotherapy. Multi-disciplinary team (MDT) to discuss whether surgery was performed 3-4 weeks after last dose of therapy. Surgery was performed 4-6 weeks after last dose of induction therapy. RNA-seq and WES were performed at baseline, and the tumor samples were also collected for RNA-seq after surgery. Based on bioinformatics analysis, we want to find better biomarker to stratified patients and explore optimized regimens for unresectable stage III NSCLC.
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The objective is to assess the efficacy and safety of precision induction therapies in patients with unresectable stage III NSCLC selected based on tumor PD-L1 expression. Patients were stratified into groups receiving Sintilimab monotherapy, Sintilimab plus IBI305, or Sintilimab combined with chemotherapy. Multi-disciplinary team (MDT) to discuss whether surgery was performed 3-4 weeks after last dose of therapy. Surgery was performed 4-6 weeks after last dose of induction therapy. This data set includes RNA-seq and WES data. The tissue collected from baseline patietns were send for RNA-seq and WES, and the tumor samples collected after surgery were send for RNA-seq only.
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