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抗体美登素偶联物的肝毒性:临床前和临床研究结果综述。

Hepatotoxicity with antibody maytansinoid conjugates: A review of preclinical and clinical findings.

机构信息

Novartis Pharmaceuticals Inc., East Hanover, NJ, USA.

MedImmune, AstraZeneca, Gaithersburg, MD, USA.

出版信息

J Appl Toxicol. 2018 May;38(5):600-615. doi: 10.1002/jat.3582. Epub 2018 Feb 1.

Abstract

Maytansinoids, the potent cytotoxic derivatives of the alkaloid maytansine are used as payloads in antibody maytansinoid conjugates. This article reviews clinical and preclinical hepatotoxicity observed with antibody maytansinoid conjugates used to treat cancer. Specific aspects of drug distribution, metabolism and excretion that may impact hepatotoxicity are reviewed vis-à-vis the kind of maytansinoid in the conjugate, cleavable or non-cleavable linkers, linker-payload combinations, drug to antibody ratio, metabolite formation, hepatic enzyme induction in relation to drug-drug interactions and species, age and gender differences. The article also sheds light on factors that may protect the liver from toxic insults.

摘要

美登素类是美登碱的强效细胞毒性衍生物,被用作抗体美登素偶联物的有效载荷。本文综述了用于治疗癌症的抗体美登素偶联物所观察到的临床前和临床肝毒性。根据偶联物中的美登素类、可裂解或不可裂解的连接子、连接子-有效载荷组合、药物与抗体的比率、代谢物形成、与药物相互作用和种属、年龄和性别相关的肝酶诱导等方面,讨论了可能影响肝毒性的药物分布、代谢和排泄的具体方面。本文还阐明了可能保护肝脏免受毒性损伤的因素。

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