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Target Oncol. 2023 Nov;18(6):965-972. doi: 10.1007/s11523-023-01007-y. Epub 2023 Nov 9.
Durvalumab (Imfinzi), a therapeutic human monoclonal antibody which binds to and blocks the activity of the immunosuppressive programmed death-ligand 1 (PD-L1) protein, is approved in the USA, EU, Japan and other countries in combination with gemcitabine and cisplatin for adults with advanced biliary tract cancer. In the pivotal phase 3 TOPAZ-1 trial, durvalumab plus gemcitabine and cisplatin significantly prolonged overall survival and progression-free survival compared with placebo plus gemcitabine and cisplatin in adults with advanced biliary tract cancer. Benefit from durvalumab was seen irrespective of primary tumour location, disease status at diagnosis (unresectable or recurrent), or initial levels of PD-L1 expression. The tolerability of durvalumab plus gemcitabine and cisplatin was manageable. Overall, the addition of durvalumab to gemcitabine and cisplatin is a valuable new treatment option for adults with advanced biliary tract cancer.
度伐利尤单抗(英飞凡)是一种人源化单克隆抗体,可与免疫抑制性程序性死亡配体 1(PD-L1)蛋白结合并阻断其活性,已在美国、欧盟、日本和其他国家获得批准,与吉西他滨和顺铂联合用于治疗晚期胆道癌成人患者。在关键性 3 期 TOPAZ-1 试验中,与安慰剂联合吉西他滨和顺铂相比,度伐利尤单抗联合吉西他滨和顺铂显著延长了晚期胆道癌成人患者的总生存期和无进展生存期。无论肿瘤原发部位、诊断时的疾病状态(不可切除或复发性)或初始 PD-L1 表达水平如何,均可观察到度伐利尤单抗的获益。度伐利尤单抗联合吉西他滨和顺铂的耐受性可管理。总体而言,度伐利尤单抗联合吉西他滨和顺铂为晚期胆道癌成人患者提供了一种有价值的新治疗选择。