在IB-IIIA期非小细胞肺癌(IMpower010)切除化疗后使用Atezolizumab的5年生存率:一项开放标签,随机,III期试验

IF 41.9 1区 医学 Q1 ONCOLOGY
Journal of Clinical Oncology Pub Date : 2025-07-20 Epub Date: 2025-05-30 DOI:10.1200/JCO-24-01681
Enriqueta Felip, Nasser Altorki, Caicun Zhou, Eric Vallières, Tibor Csoszi, Ihor O Vynnychenko, Oleksandr Goloborodko, Achim Rittmeyer, Martin Reck, Alex Martinez-Marti, Hirotsugu Kenmotsu, Yuh-Min Chen, Antonio Chella, Shunichi Sugawara, Chenqi Fu, Marcus Ballinger, Yu Deng, Minu K Srivastava, Elizabeth Bennett, Barbara J Gitlitz, Heather A Wakelee
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引用次数: 0

摘要

IMpower010 (ClinicalTrials.gov identifier: NCT02486718)先前显示,atezolizumab可改善切除的非小细胞肺癌(NSCLC)患者辅助化疗后的无病生存期(DFS),而不是最佳支持治疗(BSC)。我们报告了DFS最终分析、第二次总生存期(OS)中期分析和≥5年随访的安全性。完全切除的IB-IIIA期NSCLC患者在铂基化疗后随机分配到atezolizumab (1200 mg,每3周1次,16个周期)或BSC。在临床截止日期(2024年1月26日),分层风险比(hr;95% CI)为0.85 (95% CI, 0.71 ~ 1.01;在意向治疗(n = 1005)中P = 0.07),在全随机II-IIIA期(n = 882)中P = 0.83 (95% CI, 0.69至1.00),在II-IIIA期PD-L1肿瘤细胞(TC)≥1% (n = 476)人群中P = 0.70 (95% CI, 0.55至0.91)。OS的分层hr (95% CI)分别为0.97 (95% CI, 0.78 ~ 1.22)、0.94 (95% CI, 0.75 ~ 1.19)和0.77 (95% CI, 0.56 ~ 1.06)。II-IIIA期PD-L1 TC≥50%人群(n = 229)的未分层HRs (95% CI)为DFS的0.48 (95% CI, 0.32至0.72),OS的0.47 (95% CI, 0.28至0.77),II-IIIA期PD-L1 TC≥50%且无EGFR/ALK改变的人群(n = 209)的未分层HRs为0.49 (95% CI, 0.32至0.75)和0.44 (95% CI, 0.26至0.74)。没有新的安全信号报道。IMpower010是首个报告≥5年随访的生存结果的研究,并继续显示atezolizumab与BSC在切除的II-IIIA期pd - l1选择性NSCLC患者的辅助化疗后获益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Five-Year Survival Outcomes With Atezolizumab After Chemotherapy in Resected Stage IB-IIIA Non-Small Cell Lung Cancer (IMpower010): An Open-Label, Randomized, Phase III Trial.

IMpower010 (ClinicalTrials.gov identifier: NCT02486718) previously showed that atezolizumab improved disease-free survival (DFS) versus best supportive care (BSC) after adjuvant chemotherapy in patients with resected non-small cell lung cancer (NSCLC). We report DFS final analysis, second overall survival (OS) interim analysis, and safety with a ≥5-year follow-up. Patients with completely resected stage IB-IIIA NSCLC were randomly assigned to atezolizumab (1,200 mg once every 3 weeks, 16 cycles) or BSC after platinum-based chemotherapy. At clinical cutoff (January 26, 2024), stratified hazard ratios (HRs; 95% CI) for DFS were 0.85 (95% CI, 0.71 to 1.01; P = .07) in the intention-to-treat (n = 1,005), 0.83 (95% CI, 0.69 to 1.00) in the all-randomized stage II-IIIA (n = 882), and 0.70 (95% CI, 0.55 to 0.91) in stage II-IIIA PD-L1 tumor cell (TC) ≥1% (n = 476) populations. Stratified HRs (95% CI) for OS were 0.97 (95% CI, 0.78 to 1.22), 0.94 (95% CI, 0.75 to 1.19), and 0.77 (95% CI, 0.56 to 1.06), respectively. The unstratified HRs (95% CI) in the stage II-IIIA PD-L1 TC ≥50% population (n = 229) were 0.48 (95% CI, 0.32 to 0.72) for DFS and 0.47 (95% CI, 0.28 to 0.77) for OS, and the unstratified HRs in the stage II-IIIA PD-L1 TC ≥50% without EGFR/ALK alterations (n = 209) population were 0.49 (95% CI, 0.32 to 0.75) and 0.44 (95% CI, 0.26 to 0.74). No new safety signals were reported. IMpower010 is the first study to report survival outcomes with a ≥5-year follow-up and continued to show benefit with atezolizumab versus BSC after adjuvant chemotherapy in patients with resected stage II-IIIA PD-L1-selected NSCLC.

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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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