University Institute of Clinical Chemistry, Inselspital Bern University Hospital, University of Bern, Bern, Switzerland.
Department of Clinical Pharmacology, Division of Medical Oncology and Division of Pharmacology, the Netherlands Cancer Institute, Amsterdam, the Netherlands.
Clin Pharmacol Ther. 2018 Feb;103(2):210-216. doi: 10.1002/cpt.911. Epub 2017 Nov 20.
The purpose of this guideline is to provide information for the interpretation of clinical dihydropyrimidine dehydrogenase (DPYD) genotype tests so that the results can be used to guide dosing of fluoropyrimidines (5-fluorouracil and capecitabine). Detailed guidelines for the use of fluoropyrimidines, their clinical pharmacology, as well as analyses of cost-effectiveness are beyond the scope of this document. The Clinical Pharmacogenetics Implementation Consortium (CPIC ) guidelines consider the situation of patients for which genotype data are already available (updates available at https://cpicpgx.org/guidelines/guideline-for-fluoropyrimidines-and-dpyd/).
本指南的目的是提供有关二氢嘧啶脱氢酶 (DPYD) 基因型检测临床解读的信息,以便将结果用于指导氟嘧啶类药物(5-氟尿嘧啶和卡培他滨)的剂量调整。氟嘧啶类药物的使用详细指南、其临床药理学以及成本效益分析均不在本文件范围内。临床药物遗传学实施联盟 (CPIC) 指南考虑了已获得基因型数据的患者情况(更新信息可在 https://cpicpgx.org/guidelines/guideline-for-fluoropyrimidines-and-dpyd/ 上获取)。
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Clin Pharmacol Ther. 2017-10