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纳武利尤单抗:在晚期非鳞状非小细胞肺癌中的应用评价。

Nivolumab: A Review in Advanced Nonsquamous Non-Small Cell Lung Cancer.

机构信息

Springer, Private Bag 65901, Mairangi Bay, 0754, Auckland, New Zealand.

出版信息

Drugs. 2016 Jun;76(9):969-78. doi: 10.1007/s40265-016-0589-9.

Abstract

The programmed death (PD)-1 immune checkpoint inhibitor nivolumab (Opdivo(®)) is approved in the USA for the treatment of patients with metastatic non-small cell lung cancer (NSCLC) who have progression on or after platinum-based chemotherapy and in the EU for the treatment of adults with locally advanced or metastatic NSCLC after prior chemotherapy. In previously-treated patients with advanced nonsquamous NSCLC, overall survival was significantly prolonged and the overall response rate was significantly higher in patients who received intravenous nivolumab 3 mg/kg every 2 weeks versus intravenous docetaxel in the pivotal CheckMate 057 trial. Progression-free survival did not significantly differ between patients receiving nivolumab and those receiving docetaxel. Intravenous nivolumab had a manageable adverse event profile (including immune-mediated adverse events) and was better tolerated than docetaxel in the CheckMate 057 trial. Thus, nivolumab is an important new option for use in previously-treated patients with advanced nonsquamous NSCLC.

摘要

程序性死亡 (PD)-1 免疫检查点抑制剂纳武利尤单抗(Opdivo(®))在美国被批准用于治疗在铂类化疗后进展的转移性非小细胞肺癌 (NSCLC) 患者,以及在欧盟被批准用于治疗先前化疗后局部晚期或转移性 NSCLC 的成人患者。在先前治疗的晚期非鳞状 NSCLC 患者中,与静脉注射多西他赛相比,接受每 2 周静脉注射纳武利尤单抗 3mg/kg 的患者的总生存期显著延长,总缓解率显著更高,在关键的 CheckMate 057 试验中。纳武利尤单抗组和多西他赛组之间的无进展生存期没有显著差异。在 CheckMate 057 试验中,纳武利尤单抗的不良事件谱(包括免疫介导的不良事件)可控,且耐受性优于多西他赛。因此,纳武利尤单抗是治疗先前治疗的晚期非鳞状 NSCLC 患者的一种重要的新选择。

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