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药物治疗个体化:历史、现状与未来机遇。

Individualization of drug therapy: history, present state, and opportunities for the future.

机构信息

Center for Pharmacometrics and Systems Pharmacology, Department of Pharmaceutics, University of Florida, Lake Nona, Florida, USA.

出版信息

Clin Pharmacol Ther. 2012 Oct;92(4):458-66. doi: 10.1038/clpt.2012.113. Epub 2012 Sep 5.

Abstract

Individualization of drug therapy, described as tailoring drug selection and drug dosing to a given patient, has been an objective of physicians and other health-care providers for centuries. An understanding of the pathogenesis of the disease, the mechanism of action of the drug, and exposure-response relationships provides the framework for individualization. There are many approaches to individualization: selecting an antibiotic based on minimum effective concentrations and bacterial sensitivity, population (sparse sample) pharmacokinetics, therapeutic drug monitoring and, more recently, pharmacogenomics. The goal of individualization is to optimize the efficacy of a drug, minimize its toxicity, or both. With the growth of technology and databases, drug-disease-trial models and simulation have become useful for integrating information from many different domains. Physiology-based pharmacokinetic (PBPK) models have provided a mechanistic approach to individualization, and clinical trial designs such as those involving enrichment have also enabled individualization. In the future, "-omics" technologies, vaccines, ex vivo gene therapy, and the so-called "diseases-in-a-dish" will provide additional strategies to achieve individualization.

摘要

个体化药物治疗,即根据特定患者来选择药物和调整药物剂量,是医生和其他医疗保健提供者数个世纪以来的目标。对疾病发病机制、药物作用机制和暴露-反应关系的了解为个体化治疗提供了框架。个体化治疗有许多方法:根据最小有效浓度和细菌敏感性、群体(稀疏样本)药代动力学、治疗药物监测以及最近的药物基因组学来选择抗生素。个体化治疗的目的是优化药物疗效,降低其毒性,或两者兼而有之。随着技术和数据库的发展,药物-疾病-试验模型和模拟已成为整合来自许多不同领域信息的有用工具。基于生理学的药代动力学(PBPK)模型为个体化治疗提供了一种机制方法,而涉及富集的临床试验设计也使个体化治疗成为可能。在未来,“组学”技术、疫苗、离体基因治疗和所谓的“盘中疾病”将为实现个体化治疗提供额外的策略。

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