医学
布仑妥昔单抗维多汀
临床试验
抗体-药物偶联物
药物开发
曲妥珠单抗
曲妥珠单抗
药品
癌症
药理学
内科学
抗体
免疫学
乳腺癌
单克隆抗体
霍奇金淋巴瘤
淋巴瘤
作者
Fiona Mack,Michael Ritchie,Puja Sapra
标识
DOI:10.1053/j.seminoncol.2014.08.001
摘要
Antibody-drug conjugates (ADCs) represent a promising therapeutic modality for the clinical management of cancer. The recent approvals of brentuximab vedotin and ado-trastuzumab emtansine plus emerging data for many molecules in clinical trials highlight the potential for ADCs to offer new therapeutic options for patients. Currently, more than 30 ADCs are being evaluated in early- or late-stage clinical trials. Accordingly, much has been done to refine and transform the early-generation ADCs to the highly effective products that we now have in clinical development. These changes include a better understanding of optimal target selection, advances in antibody engineering, improvements in linker/payload conjugation strategies, and the generation of highly potent ADC payloads. In this review, we detail the current status of ADCs in both preclinical and clinical development, highlight technological advancements in ADC development, and speculate towards the future of this targeted therapeutic platform.
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