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Lakartidningen ; 1182021 Aug 10.
Artigo em Sueco | MEDLINE | ID: mdl-34498246

RESUMO

5-fluorouracil (5-FU) is still a cornerstone in drug treatment for cancer. Some patients starting standard dosed 5-FU will experience severe adverse events (SAEs). One mechanism behind SAEs is impaired dihydropyrimidine dehydrogenase (DPD) activity, resulting in an accumulation of cytotoxic metabolites. Pre-emptive testing of DPD enzyme activity or genetic variation in its gene, DPYD,  is recommended since 2020 in Sweden. We report experience from DPYD testing in 368 patients planned for 5-FU treatment. DPYD variants associated with reduced DPD activity were observed in 28 patients (8%), which is close to the expected frequency. These patients tolerated 5-FU treatment when doses were reduced according to guidelines. However, 4 out of 5 variant allele carriers starting 5-FU at standard dose due to late arrival of test results experienced SAEs. Pre-emptive testing was calculated to be cost saving and thus beneficial from a healthcare economy perspective.


Assuntos
Fluoruracila , Neoplasias , Antimetabólitos Antineoplásicos/efeitos adversos , Redução de Custos , Atenção à Saúde , Di-Hidrouracila Desidrogenase (NADP)/genética , Detecção Precoce de Câncer , Fluoruracila/efeitos adversos , Custos de Cuidados de Saúde , Humanos , Neoplasias/tratamento farmacológico , Neoplasias/genética , Testes Farmacogenômicos , Suécia
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