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基于药物遗传学的个性化治疗:法国药物遗传学网络(RNPGx)的证据水平与建议

Pharmacogenetics-based personalized therapy: Levels of evidence and recommendations from the French Network of Pharmacogenetics (RNPGx).

作者信息

Picard Nicolas, Boyer Jean-Christophe, Etienne-Grimaldi Marie-Christine, Barin-Le Guellec Chantal, Thomas Fabienne, Loriot Marie-Anne

机构信息

Service de pharmacologie, toxicologie et pharmacovigilance, centre de biologie et de recherche en santé, CHU de Limoges, 2, avenue Martin-Luther-King, 87042 Limoges, France.

Unité de toxicologie et plateforme de génétique moléculaire des cancers, laboratoire de biochimie, CHU Carémeau, 30900 Nîmes, France.

出版信息

Therapie. 2017 Apr;72(2):185-192. doi: 10.1016/j.therap.2016.09.014. Epub 2017 Jan 30.

Abstract

More than 50 laboratories offer pharmacogenetic testing in France. These tests are restricted to a limited number of indications: prevention of serious adverse drug reactions; choice of most appropriate therapeutic option; dose adjustment for a specific drug. A very small proportion of these tests are mentioned in drug information labeling and the data provided (if any) are generally insufficient to ascertain whether a test is required and if it is useful. This article discusses the rationale for evaluating the performance and clinical usefulness of pharmacogenetics and provides, on behalf of the French national network of pharmacogenetics (RNPGx), three levels of recommendation for testing: essential, advisable, and possibly helpful.

摘要

在法国,有50多个实验室提供药物遗传学检测。这些检测仅限于有限的几种适应症:预防严重药物不良反应;选择最合适的治疗方案;特定药物的剂量调整。药物信息标签中提及的此类检测比例非常小,而且所提供的数据(如果有的话)通常不足以确定是否需要进行检测以及检测是否有用。本文讨论了评估药物遗传学性能和临床实用性的基本原理,并代表法国国家药物遗传学网络(RNPGx)提供了三个检测推荐级别:必要、建议和可能有用。

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