医学
回顾性队列研究
肺癌
不利影响
肿瘤科
内科学
队列
免疫系统
比例危险模型
阶段(地层学)
癌症
队列研究
免疫学
生物
古生物学
作者
John Hunting,Sarah N. Price,Andrew T. Faucheux,Eric C. Olson,Catherine A. Elko,Alexander M. Quattlebaum,Jimmy Ruiz,Thomas Lycan
出处
期刊:Immunotherapy
[Future Medicine]
日期:2025-01-23
卷期号:: 1-6
标识
DOI:10.1080/1750743x.2025.2456448
摘要
Prior research indicates a connection between immune-related adverse events (irAEs) and improved progression-free survival (PFS) and overall survival (OS) in non-small cell lung cancer. However, limited data exists for extensive stage small cell lung cancer (ES-SCLC). This study included all ES-SCLC patients who received at least one dose of an immune checkpoint inhibitor between 2 January 2011 and 4 July 2022 using a large retrospective registry from a single institution. PFS and OS were right-censored at the date of last follow-up and were estimated using the Kaplan-Meier method. Differences in PFS and OS between irAE groups were assessed using Cox proportional hazards models. Among 245 patients with ES-SCLC; 56 (23%) experienced irAEs, 24 (42.9%) of which were high-grade (3-4). High-grade irAEs occurred at a median of 1.2 months (interquartile range [IQR] 0.45-2.5), while low-grade irAE occurred at 2.8 months (1.3-5.2). PFS was significantly longer among any irAE vs none (HR = 0.49; [95%CI 0.32-0.77]) as was OS (HR = 0.49; [95%CI 0.34-0.72]). In ES-SCLC patients treated with immunotherapy, those who experienced any irAE demonstrated a two-fold increase in both PFS and OS compared to those without an irAE. This is consistent with other tumor primaries.
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