Atezolizumab in Combination With Carboplatin and Nab-Paclitaxel in Advanced Squamous NSCLC (IMpower131): Results From a Randomized Phase III Trial

医学 阿替唑单抗 卡铂 危险系数 肿瘤科 内科学 人口 随机对照试验 紫杉醇 置信区间 化疗 癌症 顺铂 彭布罗利珠单抗 免疫疗法 环境卫生
作者
Robert M. Jotte,Federico Cappuzzo,Ihor Vynnychenko,Daniil Stroyakovskiy,Delvys Rodríguez‐Abreu,Maen Hussein,Ross A. Soo,Henry Jacob Conter,Toshiyuki Kozuki,Kuan-Chieh Huang,Vilma Graupner,Shawn W. Sun,Tien Hoang,Helen Jessop,Mark L. McCleland,Marcus Ballinger,Alan Sandler,Mark A. Socinski
出处
期刊:Journal of Thoracic Oncology [Elsevier]
卷期号:15 (8): 1351-1360 被引量:575
标识
DOI:10.1016/j.jtho.2020.03.028
摘要

Cytotoxic agents have immunomodulatory effects, providing a rationale for combining atezolizumab (anti-programmed death-ligand 1 [anti-PD-L1]) with chemotherapy. The randomized phase III IMpower131 study (NCT02367794) evaluated atezolizumab with platinum-based chemotherapy in stage IV squamous NSCLC.A total of 1021 patients were randomized 1:1:1 to receive atezolizumab+carboplatin+paclitaxel (A+CP) (n = 338), atezolizumab+carboplatin+nab-paclitaxel (A+CnP) (n = 343), or carboplatin+nab-paclitaxel (CnP) (n = 340) for four or six 21-day cycles; patients randomized to the A+CP or A+CnP arms received atezolizumab maintenance therapy until progressive disease or loss of clinical benefit. The coprimary end points were investigator-assessed progression-free survival (PFS) and overall survival (OS) in the intention-to-treat (ITT) population. The secondary end points included PFS and OS in PD-L1 subgroups and safety. The primary PFS (January 22, 2018) and final OS (October 3, 2018) for A+CnP versus CnP are reported.PFS improvement with A+CnP versus CnP was seen in the ITT population (median, 6.3 versus 5.6 mo; hazard ratio [HR] = 0.71, 95% confidence interval [CI]: 0.60-0.85; p = 0.0001). Median OS in the ITT population was 14.2 and 13.5 months in the A+CnP and CnP arms (HR = 0.88, 95% CI: 0.73-1.05; p = 0.16), not reaching statistical significance. OS improvement with A+CnP versus CnP was observed in the PD-L1-high subgroup (HR = 0.48, 95% CI: 0.29-0.81), despite not being formally tested. Treatment-related grade 3 and 4 adverse events and serious adverse events occurred in 68.0% and 47.9% (A+CnP) and 57.5% and 28.7% (CnP) of patients, respectively.Adding atezolizumab to platinum-based chemotherapy significantly improved PFS in patients with first-line squamous NSCLC; OS was similar between the arms.
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