Hanna K S
Assistant Professor of Pharmacy, Mayo Clinic College of Medicine, Oncology Pharmacy Manager, University of Minnesota Medical Center, Maple Grove, Minnesota, USA.
Drugs Today (Barc). 2020 May;56(5):329-335. doi: 10.1358/dot.2020.56.5.3127027.
The antibody-drug conjugate enfortumab vedotin is a fully humanized monoclonal antibody targeting Nectin-4 linked to a microtubule-disrupting agent, monomethyl auristatin E, via a protease-cleavable maleimidocaproyl valine-citrulline linker. In this article, we provide a comprehensive review of the preclinical and clinical activity of enfortumab vedotin, which has been recently approved in the U.S. for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma who have previously received a programmed cell death protein 1 (PD-1)/programmed cell death 1 ligand 1 (PD-L1) inhibitor as well as platinum-containing chemotherapy in the neoadjuvant/adjuvant, locally advanced or metastatic setting. Enfortumab vedotin is the first antibody-drug conjugate approved for patients with urothelial carcinoma.
抗体药物偶联物安罗替尼是一种完全人源化的单克隆抗体,靶向Nectin-4,通过可被蛋白酶切割的马来酰亚胺己酰缬氨酸-瓜氨酸连接子与微管破坏剂单甲基奥瑞他汀E相连。在本文中,我们全面综述了安罗替尼的临床前和临床活性,该药最近在美国被批准用于治疗局部晚期或转移性尿路上皮癌的成年患者,这些患者此前在新辅助/辅助、局部晚期或转移性治疗中接受过程序性细胞死亡蛋白1(PD-1)/程序性细胞死亡配体1(PD-L1)抑制剂以及含铂化疗。安罗替尼是首个被批准用于尿路上皮癌患者的抗体药物偶联物。