阿替唑单抗
多西紫杉醇
医学
内科学
危险系数
不利影响
肿瘤科
肺癌
置信区间
人口
临床研究阶段
癌症
临床试验
免疫疗法
无容量
环境卫生
作者
Louis Fehrenbacher,Joachim von Pawel,Keunchil Park,Achim Rittmeyer,David R. Gandara,Santiago Ponce Aix,Ji‐Youn Han,Shirish M. Gadgeel,Toyoaki Hida,Diego Cortinovis,Manuel Cobo,Dariusz Kowalski,Filippo de Marinis,Mayank Gandhi,Bradford J. Danner,Christina Matheny,Marcin Kowanetz,Pei He,Federico Felizzi,Hina Patel,Alan Sandler,Marcus Ballinger,Fabrice Barlési
标识
DOI:10.1016/j.jtho.2018.04.039
摘要
IntroductionThe efficacy and safety of atezolizumab versus the efficacy and safety of docetaxel as second- or third-line treatment in patients with advanced NSCLC in the primary (n = 850) and secondary (n = 1225) efficacy populations of the randomized phase III OAK study (respectively referred to as the intention-to-treat [ITT] 850 [ITT850] and ITT1225) at an updated data cutoff were assessed.MethodsPatients received atezolizumab, 1200 mg, or docetaxel, 75 mg/m2, intravenously every 3 weeks until loss of clinical benefit or disease progression, respectively. The primary end point was overall survival (OS) in the ITT population and programmed death-ligand 1–expressing subgroup. A sensitivity analysis was conducted to evaluate the impact of subsequent immunotherapy use in the docetaxel arm on the observed survival benefit with atezolizumab.ResultsAtezolizumab demonstrated an OS benefit versus docetaxel in the updated ITT850 (hazard ratio [HR] = 0.75, 95% confidence interval: 0.64–0.89, p = 0.0006) and the ITT1225 (HR = 0.80, 95% confidence interval: 0.70–0.92, p = 0.0012) after minimum follow-up times of 26 and 21 months, respectively. Improved survival with atezolizumab was observed across programmed death-ligand 1 and histological subgroups. In the immunotherapy sensitivity analysis, the relative OS benefit with atezolizumab was slightly greater in the ITT850 (HR = 0.69) and ITT1225 (HR = 0.74) than the conventional OS estimate. Fewer patients receiving atezolizumab experienced grade 3 or 4 treatment-related adverse events (14.9%) than did patients receiving docetaxel (42.4%); no grade 5 adverse events related to atezolizumab were observed.ConclusionsThe results of the updated ITT850 and initial ITT1225 analyses were consistent with those of the primary efficacy analysis demonstrating survival benefit with atezolizumab versus with docetaxel. Atezolizumab continued to demonstrate a favorable safety profile after longer treatment exposure and follow-up.
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