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

机译:Nivolumab:晚期非鳞状非小细胞肺癌的审查。

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摘要

The programmed death (PD)-1 immune checkpoint inhibitor nivolumab (Opdivo (R)) 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.
机译:程序性死亡(PD)-1免疫检查点抑制剂nivolumab(Opdivo(R))已在美国获准用于治疗转移性非小细胞肺癌(NSCLC)的患者,这些患者在基于铂的化学疗法和在欧盟接受过化疗后,用于治疗局部晚期或转移性NSCLC成人。在关键的CheckMate 057试验中,每2周接受静脉注射nivolumab 3 mg / kg的患者与接受多西他赛治疗的患者相比,先前接受治疗的晚期非鳞状NSCLC患者的总生存期显着延长,总反应率明显更高。接受nivolumab的患者和接受多西他赛的患者的无进展生存期无显着差异。在CheckMate 057试验中,静脉用药nivolumab具有可控的不良事件(包括免疫介导的不良事件),并且比多西他赛耐受性更好。因此,对于接受过治疗的晚期非鳞状非小细胞肺癌患者,nivolumab是一个重要的新选择。

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