Cavaille François, Peretti Mathieu, Garcia Marie Eve, Giorgi Roch, Ausias Nathalie, Vanelle Patrice, Barlesi Fabrice, Montana Marc
Oncopharma, AP-HM, Hôpital Nord, Marseille, France.
Oncologie Multidisciplinaire et Innovations Thérapeutiques, Aix Marseille Université, CNRS, INSERM, CRCM, AP-HM, Marseille, France.
Tumori. 2021 Feb;107(1):32-38. doi: 10.1177/0300891620926244. Epub 2020 May 27.
Pembrolizumab, a humanized immunoglobulin monoclonal antibody directed against the programmed cell death 1 receptor, demonstrated robust efficacy and a manageable safety profile across multiple tumor types in clinical trials.
To investigate the efficacy and safety of first-line pembrolizumab for patients with non-small cell lung cancers (NSCLCs) in clinical practice.
In this observational monocentric retrospective study, 38 patients with PD-L1 >50% were enrolled between November 2017 and November 2018.
The global median overall survival was 11.08 months (95% confidence interval [CI], 5.98-not reached) and the global median progression-free survival was 6 months (95% CI, 3-not reached). In the univariate analysis, clinical performance status score and the development of immune-related adverse events were the only 2 clinical factors significantly correlated with overall survival.
The results of the present study suggest that pembrolizumab seems less effective in the real-life population than in the pivotal clinical trials in patients with NSCLC but remains an effective treatment option for patients with NSCLC. Longer follow-up is needed.
帕博利珠单抗是一种针对程序性细胞死亡1受体的人源化免疫球蛋白单克隆抗体,在临床试验中对多种肿瘤类型均显示出强大的疗效和可控的安全性。
在临床实践中研究一线使用帕博利珠单抗治疗非小细胞肺癌(NSCLC)患者的疗效和安全性。
在这项观察性单中心回顾性研究中,2017年11月至2018年11月期间纳入了38例程序性死亡配体1(PD-L1)>50%的患者。
总体中位总生存期为11.08个月(95%置信区间[CI],5.98 - 未达到),总体中位无进展生存期为6个月(95%CI,3 - 未达到)。在单因素分析中,临床性能状态评分和免疫相关不良事件的发生是仅有的2个与总生存期显著相关的临床因素。
本研究结果表明,在现实人群中,帕博利珠单抗对NSCLC患者的疗效似乎低于关键临床试验中的疗效,但对NSCLC患者而言仍是一种有效的治疗选择。需要进行更长时间的随访。