医学
危险系数
内科学
中期分析
肺癌
安慰剂
临床终点
化疗
肿瘤科
无进展生存期
不利影响
外科
胃肠病学
置信区间
随机对照试验
病理
替代医学
作者
Zhijie Wang,Lin Wu,Baolan Li,Ying Cheng,Xiaoling Li,Xicheng Wang,Liang Han,Xiaohong Wu,Yun Fan,Yan Yu,Dongqing Lv,Jianhua Shi,Jianjin Huang,Shaozhang Zhou,Baohui Han,Guogui Sun,Qisen Guo,Youxin Ji,Xiaoli Zhu,Sheng Hu
摘要
PURPOSE: The CHOICE-01 study investigated the efficacy and safety of toripalimab in combination with chemotherapy as a first-line treatment for advanced non-small-cell lung cancer (NSCLC). PATIENTS AND METHODS: mutations were randomly assigned 2:1 to receive toripalimab 240 mg (n = 309) or placebo (n = 156) once every 3 weeks in combination with chemotherapy for 4-6 cycles, followed by the maintenance of toripalimab or placebo once every 3 weeks plus standard care. Stratification factors included programmed death ligand-1 expression status, histology, and smoking status. The primary end point was progression-free survival (PFS) by investigator per RECIST v1.1. Secondary end points included overall survival and safety. RESULTS: values ≤ .001). CONCLUSION: Toripalimab plus chemotherapy significantly improves PFS and OS in patients with treatment-naive advanced NSCLC while having a manageable safety profile. Subgroup analysis showed the OS benefit was mainly driven by the nonsquamous subpopulation.
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