Beyond cytotoxic potency: disposition features required to design ADC payload.

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY Xenobiotica Pub Date : 2024-08-01 Epub Date: 2024-09-27 DOI:10.1080/00498254.2024.2381139
Hao Sun, Larry C Wienkers, Anthony Lee
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Abstract

1. Antibody-drug conjugates (ADCs) have demonstrated impressive clinical usefulness in treating several types of cancer, with the notion of widening of the therapeutic index of the cytotoxic payload through the minimisation of the systemic toxicity. Therefore, choosing the most appropriate payload molecule is a particularly important part of the early design phase of ADC development, especially given the highly competitive environment ADCs find themselves in today.2. The focus of the current review is to describe critical attributes/considerations needed in the discovery and ultimately development of cytotoxic payloads in support of ADC design. In addition to potency, several key dispositional characteristics including solubility, permeability and bystander effect, pharmacokinetics, metabolism, and drug-drug interactions, are described as being an integral part of the integrated activities required in the design of clinically safe and useful ADC therapeutic agents.

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超越细胞毒性效力:设计 ADC 有效载荷所需的处置特征。
抗体-药物共轭物(ADCs)在治疗多种类型癌症方面的临床疗效令人印象深刻,其理念是通过最大限度地降低全身毒性来扩大细胞毒性有效载荷的治疗指数。因此,在 ADC 开发的早期设计阶段,选择最合适的有效载荷分子尤为重要,尤其是考虑到 ADC 目前所处的激烈竞争环境。本综述的重点是描述在发现并最终开发细胞毒性有效载荷以支持 ADC 设计过程中所需的关键属性/考虑因素。除药效外,还介绍了一些关键的处置特性,包括溶解性、渗透性和旁观者效应、药代动力学、新陈代谢和药物间相互作用,它们是设计临床上安全有用的 ADC 治疗剂所需的综合活动的组成部分。
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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来源期刊
Xenobiotica
Xenobiotica 医学-毒理学
CiteScore
3.80
自引率
5.60%
发文量
96
审稿时长
2 months
期刊介绍: Xenobiotica covers seven main areas, including:General Xenobiochemistry, including in vitro studies concerned with the metabolism, disposition and excretion of drugs, and other xenobiotics, as well as the structure, function and regulation of associated enzymesClinical Pharmacokinetics and Metabolism, covering the pharmacokinetics and absorption, distribution, metabolism and excretion of drugs and other xenobiotics in manAnimal Pharmacokinetics and Metabolism, covering the pharmacokinetics, and absorption, distribution, metabolism and excretion of drugs and other xenobiotics in animalsPharmacogenetics, defined as the identification and functional characterisation of polymorphic genes that encode xenobiotic metabolising enzymes and transporters that may result in altered enzymatic, cellular and clinical responses to xenobioticsMolecular Toxicology, concerning the mechanisms of toxicity and the study of toxicology of xenobiotics at the molecular levelXenobiotic Transporters, concerned with all aspects of the carrier proteins involved in the movement of xenobiotics into and out of cells, and their impact on pharmacokinetic behaviour in animals and manTopics in Xenobiochemistry, in the form of reviews and commentaries are primarily intended to be a critical analysis of the issue, wherein the author offers opinions on the relevance of data or of a particular experimental approach or methodology
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