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Comparing the Efficacy and Safety of a New Additional Treatment With Tislelizumab in Non-Small Cell Lung Cancer (NSCLC)

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研究单位: [1]BeiGene [2]Sichuan Cancer Hospital Chengdu,Sichuan,China,610042 [3]General Hospital of Tianjin Medical University Tianjin,Tianjin,China,300070 [4]Tianjin Medical University Cancer Institute and Hospital Tianjin,Tianjin,China [5]Yunnan Cancer Hospital Kunming,Yunnan,China [6]The Second Affiliated Hospital of Zhejiang University School of Medicine Hangzhou,Zhejiang,China,310009 [7]Zhejiang Cancer Hospital Hangzhou,Zhejiang,China,310022 [8]The First Affiliated Hospital of College of Medicine,Zhejiang University Hangzhou,Zhejiang,China [9]Ningbo No.2 Hospital Ningbo,Zhejiang,China [10]Sun Yat-sen University - Cancer Center (SYSUCC) Guangzhou,China,510060

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The primary objective of this study is to evaluate and compare major pathological response(MPR) rate and event-free survival (EFS) in participants receiving tislelizumab plus platinum-based doublet chemotherapy as the new additional treatment followed by tislelizumab as adjuvant treatment versus participants receiving placebo plus platinum-based doublet chemotherapy as neoadjuvant treatment followed by placebo as adjuvant treatment.

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