Real-world outcomes with durvalumab after chemoradiotherapy in patients with unresectable stage III NSCLC: interim analysis of overall survival from PACIFIC-R

杜瓦卢马布 中期分析 养生 放化疗 阶段(地层学) 医学 肿瘤科 内科学 随机对照试验 癌症 古生物学 免疫疗法 无容量 生物
作者
Andrea Riccardo Filippi,Jair Bar,C. Chouaid,Daniel C. Christoph,John K. Field,R. Fietkau,M.C. Garassino,Pilar Garrido,Vilde Drageset Haakensen,Steven Kao,B. Markman,F. McDonald,F. Mornex,Mor Moskovitz,Stefan O. Peters,Anne Sibille,Shankar Siva,M. van den Heuvel,Piet Vercauter,S. Anand,P. Chander,M. Licour,Alexander A.L. Jorge,Y. Qiao,Noémie Girard
出处
期刊:ESMO open [Elsevier]
卷期号:9 (6): 103464-103464 被引量:1
标识
DOI:10.1016/j.esmoop.2024.103464
摘要

•The PACIFIC trial established durvalumab after CRT as a global standard of care for unresectable stage III NSCLC.•PACIFIC-R is an observational study of a cohort of patients who received durvalumab through an early access program.•PACIFIC-R data are broadly consistent with outcomes from PACIFIC and real-world studies of the PACIFIC regimen.•Encouraging outcomes were observed across subgroups, including among patients who received sCRT and with PD-L1 TCs <1%.•These outcomes support continued use of the PACIFIC regimen as a global standard of care for unresectable stage III NSCLC. BackgroundBased on the findings of the PACIFIC trial, consolidation durvalumab following platinum-based chemoradiotherapy (CRT) is a global standard of care for patients with unresectable, stage III non-small-cell lung cancer (NSCLC). An earlier analysis from the ongoing PACIFIC-R study (NCT03798535) demonstrated the effectiveness of this regimen in terms of progression-free survival (PFS). Here, we report the first planned overall survival (OS) analysis.Patients and methodsPACIFIC-R is an observational/non-interventional, retrospective study of patients with unresectable, stage III NSCLC who started durvalumab (10 mg/kg intravenously every 2 weeks) within an AstraZeneca-initiated early access program between September 2017 and December 2018. Primary endpoints are OS and investigator-assessed PFS, estimated using the Kaplan–Meier method.ResultsBy 30 November 2021, the full analysis set included 1154 participants from 10 countries (median follow-up in censored patients: 38.7 months). Median OS was not reached, and the 3-year OS rate was 63.2% (95% confidence interval 60.3% to 65.9%). Three-year OS rates were numerically higher among patients with programmed death-ligand 1 (PD-L1) expression on ≥1% versus <1% of tumor cells (TCs; 67.0% versus 54.4%) and patients who received concurrent CRT (cCRT) versus sequential CRT (sCRT) (64.8% versus 57.9%).ConclusionsPACIFIC-R data continue to provide evidence for the effectiveness of consolidation durvalumab after CRT in a large, diverse, real-world population. Better outcomes were observed among patients with PD-L1 TCs ≥1% and patients who received cCRT. Nevertheless, encouraging outcomes were still observed among patients with TCs <1% and patients who received sCRT, supporting use of consolidation durvalumab in a broad population of patients with unresectable, stage III NSCLC. Based on the findings of the PACIFIC trial, consolidation durvalumab following platinum-based chemoradiotherapy (CRT) is a global standard of care for patients with unresectable, stage III non-small-cell lung cancer (NSCLC). An earlier analysis from the ongoing PACIFIC-R study (NCT03798535) demonstrated the effectiveness of this regimen in terms of progression-free survival (PFS). Here, we report the first planned overall survival (OS) analysis. PACIFIC-R is an observational/non-interventional, retrospective study of patients with unresectable, stage III NSCLC who started durvalumab (10 mg/kg intravenously every 2 weeks) within an AstraZeneca-initiated early access program between September 2017 and December 2018. Primary endpoints are OS and investigator-assessed PFS, estimated using the Kaplan–Meier method. By 30 November 2021, the full analysis set included 1154 participants from 10 countries (median follow-up in censored patients: 38.7 months). Median OS was not reached, and the 3-year OS rate was 63.2% (95% confidence interval 60.3% to 65.9%). Three-year OS rates were numerically higher among patients with programmed death-ligand 1 (PD-L1) expression on ≥1% versus <1% of tumor cells (TCs; 67.0% versus 54.4%) and patients who received concurrent CRT (cCRT) versus sequential CRT (sCRT) (64.8% versus 57.9%). PACIFIC-R data continue to provide evidence for the effectiveness of consolidation durvalumab after CRT in a large, diverse, real-world population. Better outcomes were observed among patients with PD-L1 TCs ≥1% and patients who received cCRT. Nevertheless, encouraging outcomes were still observed among patients with TCs <1% and patients who received sCRT, supporting use of consolidation durvalumab in a broad population of patients with unresectable, stage III NSCLC.
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