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Nivolumab in the treatment of metastatic squamous non-small cell lungcancer: a review of the evidence

机译:Nivolumab治疗转移性鳞状非小细胞肺癌癌症:证据回顾

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摘要

Progress in the treatment of patients with advanced stage squamous cell non-small cell lung cancer (NSCLC) has been limited. An improvement in the understanding of tumor immunosurveillance has resulted in the development of the immune checkpoint inhibitors such as nivolumab. Nivolumab (Opdivo®), a human immunoglobulin (Ig)G4 anti-programmed death (PD)-1 monoclonal antibody, was the first PD-1 inhibitor approved in the treatment of patients with advanced stage squamous cell NSCLC following platinum-based chemotherapy. CHECKMATE 017, a randomized phase III study of second-line nivolumab versus docetaxel, significantly improved overall survival (OS), progression-free survival (PFS), patient reported outcomes and the safety and tolerability favored patients treated with nivolumab. The ligand (PD-L1) expression did not predict for outcome. In this paper, we review the role of nivolumab in the treatment of NSCLC with particular attention on recent studies, ongoing combination studies, toxicity profile, current and potential predictive biomarkers.
机译:晚期鳞状细胞非小细胞肺癌(NSCLC)患者的治疗进展有限。对肿瘤免疫监视的理解的改善导致了免疫检查点抑制剂如nivolumab的开发。 Nivolumab(Opdivo ®)是一种人类免疫球蛋白(Ig)G4抗程序性死亡(PD)-1单克隆抗体,是首个被批准用于治疗晚期鳞状细胞癌的PD-1抑制剂铂类化疗后的NSCLC。 CHECKMATE 017是一项二线nivolumab与docetaxel的随机III期研究,显着改善了总生存期(OS),无进展生存期(PFS),患者报告了结局,并且安全性和耐受性偏向于接受nivolumab治疗的患者。配体(PD-L1)表达不能预测结果。在本文中,我们综述了Nivolumab在NSCLC治疗中的作用,尤其关注近期研究,正在进行的联合研究,毒性概况,当前和潜在的预测性生物标志物。

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