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群体药代动力学在抗逆转录病毒药物治疗评估中的应用及影响

Application and impact of population pharmacokinetics in the assessment of antiretroviral pharmacotherapy.

作者信息

Barrett Jeffrey S, Labbé Line, Pfister Marc

机构信息

Children's Hospital of Philadelphia and University of Pennsylvania, 19104, USA.

出版信息

Clin Pharmacokinet. 2005;44(6):591-625. doi: 10.2165/00003088-200544060-00003.

Abstract

Population pharmacokinetics has been an important technique used to explore and define relevant sources of variation in drug exposure and response in patient populations. This has been especially true in the area of antiretroviral therapy where the assurance of adequate and sustained drug exposure of multiple agents is highly correlated with therapeutic success. Population pharmacokinetic analyses across the four drug classes and 20 US FDA-approved products used to treat HIV have been published to date. The published reports were predominantly based on actual clinical trials conducted in HIV-infected patients with one or more agents administered. Modelling and simulation approaches have been used in the evaluation of antiretroviral agent outcomes incorporating problematic design and analysis factors such as sparse plasma sampling, data imbalance and censored data. Additional benefits of population modelling approaches applied to the investigation of antiretroviral agents include the ability to assess dosing compliance, understanding and quantifying drug-drug interactions in order to select dosing regimens and the screening of new drug candidates. Pharmacokinetic/pharmacodynamic models have been used to characterise the relationship between drug exposure and virological and immunological response, and to predict clinical outcome. These models offer the best opportunity for individualising and optimising patient therapy, particularly when adjusted for adherence/compliance. The impact of population pharmacokinetics in the area of antiretroviral therapy can be directly assessed by its role in the validation of surrogate markers such as viral RNA load, therapeutic drug monitoring and the management of individual patient outcomes via exposure-toxicity relationships. Each of these population pharmacokinetic outcomes has contributed to the current regulatory environment, specifically in the area of accelerated approval of new antiretroviral agents.

摘要

群体药代动力学一直是用于探索和确定患者群体中药物暴露和反应相关变异来源的重要技术。在抗逆转录病毒治疗领域尤其如此,在该领域中,确保多种药物有足够且持续的药物暴露与治疗成功高度相关。迄今为止,已发表了针对用于治疗HIV的四类药物和20种美国食品药品监督管理局(FDA)批准产品的群体药代动力学分析。已发表的报告主要基于在感染HIV的患者中进行的实际临床试验,这些试验使用了一种或多种药物。建模和模拟方法已用于评估抗逆转录病毒药物的结果,其中纳入了诸如血浆采样稀疏、数据不平衡和删失数据等有问题的设计和分析因素。应用于抗逆转录病毒药物研究的群体建模方法的其他好处包括评估给药依从性的能力、理解和量化药物相互作用以选择给药方案以及筛选新的候选药物。药代动力学/药效学模型已用于表征药物暴露与病毒学和免疫学反应之间的关系,并预测临床结果。这些模型为个体化和优化患者治疗提供了最佳机会,尤其是在根据依从性/顺应性进行调整时。群体药代动力学在抗逆转录病毒治疗领域的影响可以通过其在替代标志物验证中的作用直接评估,这些替代标志物如病毒RNA载量、治疗药物监测以及通过暴露-毒性关系管理个体患者结果。这些群体药代动力学结果中的每一个都对当前的监管环境做出了贡献,特别是在新抗逆转录病毒药物加速批准领域。

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