医学
药品
药代动力学
药物输送
靶向给药
药理学
有效载荷(计算)
抗体-药物偶联物
抗体
单克隆抗体
免疫学
计算机科学
纳米技术
计算机网络
网络数据包
材料科学
作者
Edit Tarcsa,Magali Guffroy,Hadi Falahatpisheh,Colin Phipps,J. Cory Kalvass
标识
DOI:10.1016/j.ddtec.2020.07.002
摘要
Antibody-drug conjugates (ADCs) are targeted therapies with the expectation of broadened therapeutic window due to tumor-specific drug delivery. Recent approvals, including ADCs with a novel payload class, topoisomerase-1 inhibitors, generated renewed excitement in the field. We provide a critical review of approved and late-stage molecules, discuss strategies in solid tumors and ADCs outside oncology. Our pharmacokinetics-based assessment of targeting suggests that ADCs, especially in solid tumors, rely on additional mechanisms for efficacy including slow-release of the payload to the circulation at potentially efficacious levels. Further adjustments in the technology are needed to fulfill the promise of true targeted drug delivery.
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