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[Phenotype- or genotype test for dihydropyrimidin dehydrogenase deficiency before treatment with a fluoropyrimidine].
Andersen, Stig Ejdrup; Paulsen, Niels Herluf; Pfeiffer, Per; Qvortrup, Camilla; Damkier, Per.
Afiliación
  • Andersen SE; seja@regionsjaelland.dk.
Ugeskr Laeger ; 183(6)2021 02 08.
Article en Da | MEDLINE | ID: mdl-33570023
Some patients may have partial or complete deficiency of dihydropyrimidin dehydrogenase (DPD) and be more likely to experience severe toxicity with 5-fluorouracil. Since the spring of 2020, the Danish Medicines Agency has recommended genotype or phenotype testing before treatment with a fluoropyrimidine, but the most appropriate test strategy is debated. In this review, we present polymorphisms in the genes coding for DPD and summarise the evidence for DPD-enzyme deficiency testing and pharmacokinetic guided dosing.
Asunto(s)
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Banco de datos: MEDLINE Asunto principal: Deficiencia de Dihidropirimidina Deshidrogenasa Límite: Humans Idioma: Da Revista: Ugeskr Laeger Año: 2021 Tipo del documento: Article
Buscar en Google
Banco de datos: MEDLINE Asunto principal: Deficiencia de Dihidropirimidina Deshidrogenasa Límite: Humans Idioma: Da Revista: Ugeskr Laeger Año: 2021 Tipo del documento: Article