Treatment Characteristics and Real-World Progression-Free Survival in Patients With Unresectable Stage III NSCLC Who Received Durvalumab After Chemoradiotherapy: Findings From the PACIFIC-R Study

杜瓦卢马布 医学 中止 肺炎 放化疗 内科学 临床终点 危险系数 阶段(地层学) 回顾性队列研究 队列 外科 置信区间 放射治疗 临床试验 癌症 古生物学 免疫疗法 生物 无容量
作者
Nicolas Girard,Jair Bar,Pilar Garrido,Marina Chiara Garassino,Fiona McDonald,F. Mornex,Andrea Riccardo Filippi,Hans Smit,Solange Peters,John K. Field,Daniel C. Christoph,Anne Sibille,Rainer Fietkau,Vilde Drageset Haakensen,C. Chouaïd,Ben Markman,T. Jeroen N. Hiltermann,Álvaro Taus,William T. Sawyer,A. Allen,Pratibha Chander,Muriel Licour,Benjamin Solomon
出处
期刊:Journal of Thoracic Oncology [Elsevier]
卷期号:18 (2): 181-193 被引量:91
标识
DOI:10.1016/j.jtho.2022.10.003
摘要

The phase 3 PACIFIC trial established consolidation therapy with durvalumab as standard of care for patients with unresectable, stage III NSCLC and no disease progression after definitive chemoradiotherapy (CRT). The observational PACIFIC-R study assesses the real-world effectiveness of durvalumab in patients from an early access program. Here, we report treatment characteristics and a preplanned analysis of real-world progression-free survival (rwPFS).PACIFIC-R (NCT03798535) is an ongoing, international, retrospective study of patients who started durvalumab (intravenously; 10 mg/kg every 2 wk) within an early access program between September 2017 and December 2018. The primary end points are investigator-assessed rwPFS and overall survival (analyzed by Kaplan-Meier method).As of November 30, 2020, the full analysis set comprised 1399 patients from 11 countries (median follow-up duration, 23.5 mo). Patients received durvalumab for a median of 11.0 months. Median rwPFS was 21.7 months (95% confidence interval: 19.1-24.5). RwPFS was numerically longer among patients who received concurrent versus sequential CRT (median, 23.7 versus 19.3 mo) and among patients with programmed cell death-ligand 1 expression greater than or equal to 1% versus less than 1% (22.4 versus 15.6 mo). Overall, 16.5% of the patients had adverse events leading to treatment discontinuation; 9.5% of all patients discontinued because of pneumonitis or interstitial lung disease.Consolidation durvalumab after definitive CRT was well tolerated and effective in this large, real-world cohort study of patients with unresectable, stage III NSCLC. As expected, rwPFS was longer among patients who received concurrent versus sequential CRT and patients with higher programmed cell death-ligand 1 expression. Nevertheless, favorable rwPFS outcomes were observed regardless of these factors.
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