A comprehensive review of 20 years of progress in nonclinical QT evaluation and proarrhythmic assessment.

IF 2.2 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Eric Delpy, Anne-Marie Bétat, Annie Delaunois, Christophe Drieu la Rochelle, Eric Martel, Jean-Pierre Valentin
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Abstract

The assessment of drug-induced QT interval prolongation and associated proarrhythmic risks, such as Torsades de Pointes (TdP), has evolved significantly over the past decades. This review traces the development of nonclinical QT evaluation, highlighting key milestones and innovations that have shaped current practices in cardiac safety assessment. The emergence of regulatory guidelines, including International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) S7B, established a nonclinical framework for evaluating drug effects on cardiac repolarization, addressing concerns raised by drug withdrawals in the 1990s. Advances in in vitro, in vivo, and in silico models have enhanced the predictive accuracy of nonclinical studies, with the hERG assay and telemetry-based animal models becoming gold standards. Recent initiatives, such as the Comprehensive in vitro Proarrhythmia Assay (CiPA) and the Japan iPS Cardiac Safety Assessment (JiCSA), emphasize integrating mechanistic insights from human-derived cardiomyocyte models and computational approaches to refine risk predictions. The 2020s mark a shift toward integrated nonclinical-clinical risk assessments, as exemplified by the ICH E14/S7B Questions and Answers. These highlight the need of best practices for study design, data analysis, and interpretation to support regulatory decision-making. Furthermore, the adoption of New Approach Methodologies (NAMs) and reinforced adherence to 3Rs principles (Reduce, Refine, Replace) reflect a commitment to ethical and innovative safety science. This review underscores the importance of harmonized and translational approaches in cardiac safety evaluation, providing a foundation for advancing drug development while safeguarding patient safety. Future directions include further integration of advanced methodologies and regulatory harmonization to streamline nonclinical and clinical risk assessments.

非临床QT间期评估和心律失常评估20年进展综述。
在过去的几十年里,对药物引起的QT间期延长和相关的心律失常风险的评估,如扭转角(TdP),有了显著的发展。本文回顾了非临床QT评估的发展,强调了影响心脏安全评估当前实践的关键里程碑和创新。监管指南的出现,包括国际人用药品技术要求协调委员会(ICH) S7B,建立了评估药物对心脏复极影响的非临床框架,解决了20世纪90年代药物停药引起的关注。体外、体内和硅模型的进步提高了非临床研究的预测准确性,hERG测定和基于遥测的动物模型成为金标准。最近的举措,如综合体外心律失常原测定(CiPA)和日本iPS心脏安全评估(JiCSA),强调整合来自人源性心肌细胞模型和计算方法的机制见解,以完善风险预测。21世纪20年代标志着向综合非临床-临床风险评估的转变,如ICH E14/S7B问答。这些突出了对研究设计、数据分析和解释的最佳实践的需求,以支持监管决策。此外,采用新方法方法(NAMs)和加强遵守3r原则(减少,改进,替换)反映了对道德和创新安全科学的承诺。这篇综述强调了在心脏安全性评估中协调和转化方法的重要性,为推进药物开发同时保障患者安全提供了基础。未来的方向包括进一步整合先进的方法和监管协调,以简化非临床和临床风险评估。
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
CiteScore
4.90
自引率
4.00%
发文量
39
审稿时长
6-12 weeks
期刊介绍: Broadly speaking, the Journal of Pharmacokinetics and Pharmacodynamics covers the area of pharmacometrics. The journal is devoted to illustrating the importance of pharmacokinetics, pharmacodynamics, and pharmacometrics in drug development, clinical care, and the understanding of drug action. The journal publishes on a variety of topics related to pharmacometrics, including, but not limited to, clinical, experimental, and theoretical papers examining the kinetics of drug disposition and effects of drug action in humans, animals, in vitro, or in silico; modeling and simulation methodology, including optimal design; precision medicine; systems pharmacology; and mathematical pharmacology (including computational biology, bioengineering, and biophysics related to pharmacology, pharmacokinetics, orpharmacodynamics). Clinical papers that include population pharmacokinetic-pharmacodynamic relationships are welcome. The journal actively invites and promotes up-and-coming areas of pharmacometric research, such as real-world evidence, quality of life analyses, and artificial intelligence. The Journal of Pharmacokinetics and Pharmacodynamics is an official journal of the International Society of Pharmacometrics.
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