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驱动基因阴性晚期非小细胞肺癌的二线治疗
方案Ⅰ 纳武单抗
![](https://epubservercos.yuewen.com/B8A9D8/22919013101368106/epubprivate/OEBPS/Images/T64_290_2571_2050_2853_82084.jpg?sign=1739536282-jlWVtl1CKYRAGcNeNZ2oCpvfFOfQ8f0E-0-9c344a90fdb6059248e2f68d06e3f0a5)
方案评价
![](https://epubservercos.yuewen.com/B8A9D8/22919013101368106/epubprivate/OEBPS/Images/T65_226_344_1956_2227_147399.jpg?sign=1739536282-mi0lRqXwYlckvdv9Fnyow0HV5V0EJ2Dm-0-73dd2d35dedf0bad6186b5e03b7cc666)
点评
纳武单抗成为驱动基因阴性的一线化疗后疾病进展的非小细胞肺癌(NSCLC)患者的优先治疗方案(Ⅰ类)。证据来源于2项随机、开放、Ⅲ期临床研究(Checkmate 017研究和Checkmate 057研究)。纳武单抗显示出了持久的抗肿瘤活性,在所有NSCLC亚型中,纳武单抗二线治疗均能较多西他赛显著提高3年生存率。如果不适宜纳武单抗治疗,多西他赛仍可作为驱动基因阴性的晚期非小细胞肺癌二线治疗。
(吴向华)
参考文献
[1] BORGHAEI H,PAZ-ARES L,HORN L,et al.Nivolumab versus docetaxel in advanced nonsquamous nonsmall-cell lung cancer.N Engl J Med,2015,373:1627-1639.
[2] HORN L,SPIGEL DR,VOKES EE,et al.Nivolumab versus docetaxel in previously treated patients with advanced non-small-cell lung cancer:two-year outcomes from two randomized,open-label,phase Ⅲ trials(CheckMate 017 and CheckMate 057).J Clin Oncol,2017,35(35):3924-3933.