改进 ADC 安全性、药代动力学和治疗指数转化的方法。

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY Xenobiotica Pub Date : 2024-08-01 Epub Date: 2024-09-27 DOI:10.1080/00498254.2024.2352600
Qihong Huang, Minu Ravindra Pilvankar, Rakesh Dixit, Hongbin Yu
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引用次数: 0

摘要

抗体药物共轭物(ADC)是一类重要的癌症疗法。它们是由抗体、细胞毒性有效载荷和连接体组成的复杂分子。ADCs 的目的是通过靶向主要表达在肿瘤细胞表面而非正常细胞表面的独特抗原,在肿瘤内部释放强效细胞毒性药物,造成细胞毒性细胞死亡,从而具有高度特异性。尽管 ADC 对肿瘤抗原具有高度特异性,但许多 ADC 都存在靶外和靶内肿瘤外毒性,往往在取得理想的临床疗效之前就已经引发了安全性问题。因此,提高 ADCs 的治疗指数(TI)对充分发挥这种重要治疗方式的潜力至关重要。本综述总结了目前提高 ADCs 的安全性、药代动力学和治疗指数的方法。综述总结了当前提高 ADCs 的安全性、药代动力学和 TI 转化的方法。综述将讨论由脱靶和靶上毒性导致的 ADCs 常见安全性结果,以及降低 ADC 安全性风险的非临床方法;综述还将阐述使用临床前和临床剂量与暴露数据计算 TI 以指导临床用药的多种方法;综述还将讨论提高 ADCs TI 的不同方法,包括选择合适的靶点、合适的有效载荷连接剂和患者、优化理化性质以及使用分馏给药。
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Approaches to improve the translation of safety, pharmacokinetics and therapeutic index of ADCs.

1. Antibody-drug conjugates (ADCs) are an important class of cancer therapies. They are complex molecules, comprising an antibody, a cytotoxic payload, and a linker. ADCs intend to confer high specificity by targeting a unique antigen expressed predominately on the surface of the tumour cells than on the normal cells and by releasing the potent cytotoxic drug inside the tumour causing cytotoxic cell death. Despite high specificity to tumour antigens, many ADCs are associated with off-target and on-target off-tumour toxicities, often leading to safety concerns before achieving the desirable clinical efficacy. Therefore, it is crucial to improve the therapeutic index (TI) of ADCs to enable the full potential of this important therapeutic modality. 2. The review summarises current approaches to improve the translation of safety, pharmacokinetics, and TI of ADCs. Common safety findings of ADCs resulting from off-target and on-target toxicities and nonclinical approaches to de-risk ADC safety will be discussed; multiple approaches of using preclinical and clinical dose and exposure data to calculate TI to guide clinical dosing will be elaborated; different approaches to improve TI of ADCs, including selecting the right target, right payload-linker and patients, optimising physicochemical properties, and using fractionation dosing, will also be discussed.

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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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