Application of Mechanistic Mathematical Modeling to Toxicology: Quantitative Systems Toxicology (QST).

Q1 Pharmacology, Toxicology and Pharmaceutics
Kylie A Beattie, Anna Sher
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引用次数: 0

Abstract

Quantitative systems toxicology (QST) is emerging as an independent field of model-informed drug development (MIDD) with a focus on predicting toxicity endpoints. To enable toxicological predictions, QST models require incorporation of mechanistic details specific to safety applications including the ability to accurately model supratherapeutic doses and appropriately represent safety endpoints. Unique to the field of toxicology, mechanistic knowledge is often described through the use of adverse outcome pathways (AOPs), which formally represent existing knowledge about mechanisms of toxicity. The toxicities represented by QST models can arise from exaggerated or adverse pharmacological effects of engaging the drug's intended target (on-target toxicity) or from adverse events due to modulation of additional targets beyond the primary target (off-target toxicity). In cases of on-target toxicity, QST models can be considered as a type of Quantitative Systems Pharmacology (QSP) model that incorporates safety biomarkers and often includes simulations performed outside the therapeutic dose range to explore potential adverse consequences of exaggerated pharmacology in a pre-clinical or clinical setting. QST models assessing off-target toxicities can be considered distinct from QSP models in that they are typically applicable across molecules of a given modality which can (and often do) have different primary therapeutic targets. Off-target QST models commonly focus on the interrogation of general (e.g. pan-compound) toxicity mechanisms, often within a specific organ system. It can be difficult to categorize a model as purely QSP or QST (given that some models can be considered as both a QSP and a QST model), and therefore, we encourage readers to refer to a model based on its context of use and application. Thus, throughout this chapter, we refer to models as QST models when the context of use is to understand safety-related questions. To illustrate QST modeling approaches, examples of QST model applications for on-target and off-target toxicities at different stages of the drug discovery and development pipeline are presented and discussed. Additionally, contexts of use, triggers, key objectives, and potential impacts of QST models including the types of decisions QST applications can inform across drug discovery and development are reviewed. The chapter concludes with an overview of key challenges and future perspectives in the field of QST.

机械数学模型在毒理学中的应用:定量系统毒理学(QST)。
定量系统毒理学(QST)正在成为模型知情药物开发(MIDD)的一个独立领域,其重点是预测毒性终点。为了实现毒理学预测,QST模型需要结合特定于安全应用的机制细节,包括准确模拟超治疗剂量和适当表示安全终点的能力。毒理学领域的独特之处是,机制知识通常通过使用不良结果途径(AOPs)来描述,它正式代表了关于毒性机制的现有知识。QST模型所代表的毒性可能来自药物预期靶点的夸大或不良药理作用(靶毒性)或由于调节主要靶点以外的其他靶点(脱靶毒性)而引起的不良事件。在靶毒性的情况下,QST模型可以被视为定量系统药理学(QSP)模型的一种,该模型包含安全生物标志物,并且通常包括在治疗剂量范围之外进行的模拟,以探索在临床前或临床环境中夸大药理学的潜在不良后果。评估脱靶毒性的QST模型可以被认为与QSP模型不同,因为它们通常适用于给定模态的分子,这些分子可以(而且经常)具有不同的主要治疗靶点。脱靶QST模型通常侧重于询问一般(例如泛化合物)毒性机制,通常在特定器官系统内。将模型分类为纯粹的QSP或QST是很困难的(考虑到一些模型可以同时被认为是QSP和QST模型),因此,我们鼓励读者根据其使用和应用的上下文来引用模型。因此,在本章中,当使用上下文是为了理解与安全相关的问题时,我们将模型称为QST模型。为了说明QST建模方法,本文介绍并讨论了QST模型在药物发现和开发的不同阶段应用于靶标和非靶标毒性的例子。此外,还回顾了QST模型的使用背景、触发因素、关键目标和潜在影响,包括QST应用可以在药物发现和开发过程中提供信息的决策类型。本章最后概述了QST领域的主要挑战和未来前景。
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
Handbook of experimental pharmacology
Handbook of experimental pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
5.20
自引率
0.00%
发文量
54
期刊介绍: The Handbook of Experimental Pharmacology is one of the most authoritative and influential book series in pharmacology. It provides critical and comprehensive discussions of the most significant areas of pharmacological research, written by leading international authorities. Each volume in the series represents the most informative and contemporary account of its subject available, making it an unrivalled reference source.
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