医学
彭布罗利珠单抗
内科学
肺癌
队列
肿瘤科
回顾性队列研究
放射治疗
化疗
比例危险模型
癌症
免疫疗法
外科
作者
Cole Friedes,Nikhil Yegya‐Raman,Siqi Zhang,Michelle Iocolano,Roger B. Cohen,Charu Aggarwal,Jeffrey C. Thompson,Melina E. Marmarelis,William P. Levin,Keith A. Cengel,Christine Ciunci,Aditi P. Singh,Christopher D’Avella,Christiana Davis,Corey J. Langer,Steven J. Feigenberg
标识
DOI:10.1016/j.cllc.2023.09.002
摘要
The patterns of failure (POF) for metastatic non-small-cell lung cancer (mNSCLC) treated with immunotherapy are not well established.We conducted a retrospective cohort study of mNSCLC that received first-line pembrolizumab with or without chemotherapy at a single academic center from 2015 to 2021. We defined POF with 2 classifications: 1) local, regional, or distant failure, or 2) failure in existing lesions, new lesions, or a combination. Oligoprogression was defined as disease progression (PD) in ≤3 sites of failure. Overall survival (OS) was measured via Kaplan-Meier and modelled with Cox regression.Of 298 patients identified, 198 had PD. Using POF classification 1, most failures were distant (43.9%) or a combination of locoregional and distant (34.4%). For POF classification 2, failures occurred in a combination of new and existing lesions (45.0%), existing lesions alone (33.3%), or in new lesions only (21.7%). Oligoprogression occurred in 39.9% (n = 79) cases. Median OS was higher in the following: PD in existing lesions vs. new or new + existing lesions (28.7 vs. 20.2 vs. 13.9 months, P < .001) and oligoprogression vs. polyprogression (35.1 vs. 12.2 months, P < .001). In oligoprogression, median OS was better for those who received radiation to all sites of PD (62.2 months) than for those who changed systemic therapy (22.9 months, P = .007). On multivariable analysis, radiation for oligoprogression (HR 0.35, 95% CI: 0.20-0.62, P < .001) was associated with improved OS.In mNSCLC treated with pembrolizumab, oligoprogression is relatively common. Randomized data are needed to define the benefits of radiation in oligoprogressive mNSCLC.
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