抗体-药物结合作为靶向治疗:我们还在那里吗?对当前临床前景的批判性回顾

Q1 Pharmacology, Toxicology and Pharmaceutics Drug Discovery Today: Technologies Pub Date : 2020-12-01 DOI:10.1016/j.ddtec.2020.07.002
Edit Tarcsa , Magali R. Guffroy , Hadi Falahatpisheh , Colin Phipps , John C. Kalvass
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引用次数: 15

摘要

抗体-药物偶联物(adc)是一种靶向治疗方法,由于肿瘤特异性药物传递,有望拓宽治疗窗口。最近的批准,包括具有新型有效载荷类别拓扑异构酶-1抑制剂的adc,在该领域引起了新的兴奋。我们提供已批准和晚期分子的关键审查,讨论肿瘤外实体肿瘤和adc的策略。我们基于药代动力学的靶向性评估表明adc,特别是在实体肿瘤中,依赖于其他机制的疗效,包括以潜在有效水平缓慢释放有效载荷到循环中。为了实现真正靶向给药的承诺,这项技术需要进一步调整。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Antibody-drug conjugates as targeted therapies: Are we there yet? A critical review of the current clinical landscape

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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来源期刊
Drug Discovery Today: Technologies
Drug Discovery Today: Technologies Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
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期刊介绍: Discovery Today: Technologies compares different technological tools and techniques used from the discovery of new drug targets through to the launch of new medicines.
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