结合
药品
抗体
抗体-药物偶联物
内化
抗原
医学
药理学
效力
癌症
癌症研究
连接器
临床试验
单克隆抗体
免疫学
体外
化学
内科学
生物化学
计算机科学
数学分析
受体
操作系统
数学
作者
Paul J. Carter,Peter D. Senter
出处
期刊:The cancer journal
[Ovid Technologies (Wolters Kluwer)]
日期:2008-05-01
卷期号:14 (3): 154-169
被引量:400
标识
DOI:10.1097/ppo.0b013e318172d704
摘要
The antibody-drug conjugate (ADC) concept is to use an antibody to deliver a cytotoxic drug selectively to a target such as a tumor-associated antigen. Such conjugates represent a broadly applicable approach to enhance the antitumor activity of antibodies and improve the tumor-to-normal tissue selectivity of chemotherapy. Critical parameters for ADC development include target antigen selection, conjugate internalization by tumor cells, drug potency and stability of the linker between drug and antibody. Other important considerations include the conjugation methods, drug-to-antibody ratio, and the effects of drug conjugation on antibody properties. Highly potent drugs with more stable linkers have been attached to a new generation of antibodies to create conjugates with pronounced antitumor activities in preclinical studies and encouraging results in early stage clinical trials. This review details these advances, discusses some of the remaining challenges, and overviews ADCs currently in clinical trials for cancer therapy.
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