药品
药理学
医学
抗体-药物偶联物
抗体
结合
免疫学
单克隆抗体
数学分析
数学
作者
Mohammad Javad Khosravanian,Yousef Mirzaei,Ali Hussein Mer,Maryam Keyhani-Khankahdani,Fatemeh Sarina Abdinia,Fatemeh Misamogooe,Zahra Amirkhani,Nader Bagheri,Anna Meyfour,Saeed Jahandideh,Nesa Barpour,Yousef Nikmanesh,Hosein Shahsavarani,Meghdad Abdollahpour‐Alitappeh
标识
DOI:10.1016/j.lfs.2024.122910
摘要
Nectin-4 (Nectin cell adhesion molecule 4), a type I transmembrane cell adhesion protein, was demonstrated to be overexpressed in a variety of tumors, making it an attractive antigen for targeted therapies such as antibody-drug conjugates (ADCs). Of great note, the US Food and Drug Administration (FDA)-approval of the first Nectin-4-directed ADC, enfortumab vedotin (EV), in urothelial cancer (UC) not only introduced Nectin-4 as a clinically validated and reliable target antigen but also confirmed the evolving role of Nectin-4-directed ADCs as novel and promising cancer therapeutics. In addition to EV, there have been or are currently being seven and eleven Nectin-4-directed ADCs, respectively, in various stages of clinical trials and preclinical development, offering a promising future for the treatment of Nectin-4-positive cancer patients. This study reviewed clinical- and preclinical-stage Nectin-4-directed ADCs.
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