医学
无容量
内科学
银耳霉素
肿瘤科
易普利姆玛
杜瓦卢马布
临床终点
耐受性
肺癌
放化疗
随机对照试验
癌症
免疫疗法
不利影响
作者
Dirk De Ruysscher,Suresh S. Ramalingam,James J. Urbanic,David E. Gerber,Daniel S.W. Tan,Junliang Cai,Ang Li,Solange Peters
标识
DOI:10.1016/j.cllc.2021.07.005
摘要
Patients with untreated, stage III NSCLC will be randomized 1:1:1 to nivolumab plus cCRT followed by nivolumab in combination with ipilimumab (Arm A) or nivolumab alone (Arm B); or cCRT followed by durvalumab (Arm C). Primary endpoints are PFS and OS (Arm A vs. Arm C). Secondary endpoints include additional analyses of PFS and OS (Arm A vs. Arm B; Arm B vs. Arm C), as well as objective response rate, complete response rate, time to response, duration of response, time to death or distant metastases, and safety and tolerability. Recruitment began on August 20, 2019, and the estimated primary completion date is October 17, 2022.
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