阿替唑单抗
杜瓦卢马布
肿瘤科
医学
阶段(地层学)
肺癌
内科学
化疗
一线治疗
癌症
免疫疗法
无容量
生物
古生物学
作者
J.W. Shaw,Xerxes Pundole,Akhila Balasubramanian,Erik S. Anderson,M. Pastel,D. Gwyn Bebb,Tony T. Jiang,Pablo Martinez,Suresh S. Ramalingam,Hossein Borghaei
出处
期刊:Oncologist
[AlphaMed Press]
日期:2024-08-22
卷期号:29 (12): 1079-1089
被引量:7
标识
DOI:10.1093/oncolo/oyae234
摘要
Abstract Background The landscape of small cell lung cancer (SCLC) has changed since the 2019 and 2020 approvals of anti-PD-L1 atezolizumab and durvalumab for first-line (1L) treatment in combination with chemotherapy. We studied treatment patterns and real-world overall survival (rwOS) following 1L-3L therapy. Patients and Methods A nationwide electronic health record (EHR)-derived de-identified database was used to describe treatment patterns, characteristics, and survival of patients with extensive-stage (ES)-SCLC by 1L anti-PD-L1 treatment. Patients with ES-SCLC who initiated ≥1 line of systemic therapy from 2013 to 2021, with potential follow-up through 2022, were included. Results Among 9952 patients with SCLC, there were 4308 patients with ES-SCLC treated during the study period who met eligibility criteria. Etoposide + platinum (EP) chemotherapy was most common in the 1L, with addition of anti-PD-L1 therapy to most regimens by 2019. Second-line regimens varied by platinum sensitivity status and shifted from topotecan to lurbinectedin over time. Median rwOS following 1L therapy was 8.3 months (95% CI, 7.9-8.8) in those treated with 1L anti-PD-L1 and 8.0 months (95% CI, 7.8-8.2) in those who were not. Following 2L and 3L, median rwOS was 5.6 (95% CI, 4.9-6.3) and 4.9 months (95% CI, 3.4-6.0), respectively, among 1L anti-PD-L1-treated, and 4.5 (95% CI, 4.2-4.9) and 4.0 months (95% CI, 3.7-4.5), respectively, among those who were not. Conclusion Despite the introduction of frontline anti-PD-L1 therapy, survival remains dismal among patients with ES-SCLC treated in the real-world setting.
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