Clinical and molecular characterization of long-term survivors with extensive-stage small cell lung cancer treated with first-line atezolizumab plus carboplatin and etoposide

阿替唑单抗 医学 肿瘤科 内科学 安慰剂 卡铂 肺癌 依托泊苷 免疫学 免疫疗法 癌症 化疗 病理 彭布罗利珠单抗 顺铂 替代医学
作者
Stephen V. Liu,Tony Mok,Barzin Y. Nabet,Aaron S. Mansfield,Richard de Boer,György Losonczy,Shunichi Sugawara,Rafał Dziadziuszko,Maciej Bryl,Alexey Smolin,Maximilian J. Hochmair,Marina Chiara Garassino,Carl M. Gay,John V. Heymach,Lauren A. Byers,Sivuonthanh Lam,Rafael Rosell,S. Morris,Leah Adler,David S. Shames,Martin Reck
出处
期刊:Lung Cancer [Elsevier]
卷期号:186: 107418-107418 被引量:11
标识
DOI:10.1016/j.lungcan.2023.107418
摘要

ObjectivesIn the Phase I/III IMpower133 study, first-line atezolizumab plus carboplatin and etoposide (CP/ET) treatment for extensive-stage small cell lung cancer (ES-SCLC) significantly improved overall survival (OS) and progression-free survival versus placebo plus CP/ET. We explored patient and disease characteristics associated with long-term survival in IMpower133, and associations of differential gene expression and SCLC-A (ASCL1-driven), SCLC-N (NEUROD1-driven), SCLC-P (POU2F3-driven), and SCLC-inflamed (SCLC-I) transcriptional subtypes with long-term survival.Materials and MethodsPatients with previously untreated ES-SCLC were randomized 1:1 to four 21-day cycles of CP/ET with atezolizumab or placebo. Long-term survivors (LTS) were defined as patients who lived ≥ 18 months post randomization. A generalized linear model was used to evaluate the odds of living ≥ 18 months. Differential gene expression was analyzed using RNA-sequencing data in LTS and non-LTS. OS was assessed by T-effector and B-cell gene signature expression. Distribution of SCLC transcriptional subtypes was assessed in LTS and non-LTS.ResultsMore LTS were in the atezolizumab arm (34%) than in the placebo arm (20%). The odds ratio for living ≥ 18 months in the atezolizumab arm versus the placebo arm was 2.1 (P < 0.03). Enhanced immune-related signaling was seen in LTS in both arms. Exploratory OS analyses showed atezolizumab treatment benefit versus placebo across T-effector and B-cell gene signature expression subgroups. A higher proportion of LTS than non-LTS in both arms had the SCLC-I subtype; this difference was particularly pronounced in the atezolizumab arm.ConclusionThese exploratory analyses suggest that long-term survival is more likely with atezolizumab than placebo in ES-SCLC, confirming the treatment benefit of the IMpower133 regimen.ClinicalTrial.gov Identifier: NCT02763579.
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