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Lethal toxicity following standard dose of 5-FU in patients carrying DPYD c.1905+1G>A mutation (CROSBI ID 608349)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Božina, Nada ; Goršić, Irma ; Pejnović, Lana ; Badžek, Saša ; Pleština, Stjepko Lethal toxicity following standard dose of 5-FU in patients carrying DPYD c.1905+1G>A mutation // Pharmacogenomics and Theranostics in practice. 2013

Podaci o odgovornosti

Božina, Nada ; Goršić, Irma ; Pejnović, Lana ; Badžek, Saša ; Pleština, Stjepko

engleski

Lethal toxicity following standard dose of 5-FU in patients carrying DPYD c.1905+1G>A mutation

Dihydropyrimidine dehydrogenase (DPD) is the key enzyme in the detoxification of 5-fluorouracil (5-FU). Patients with DPD deficiency are at increased risk of severe toxicity from 5-FU. UGT1A1 is important for the irinotecan pharmacokinetic. DPYD c.1905+1AA mutation is known to result in DPD deficiency which is the cause of severe adverse and sometimes lethal reactions to 5-FU. UGT1A1 is also important for the irinotecan pharmacokinetic. The genotyping of cancer patients for DPYD and irinotecan gene variants prior to administration of 5-FU would be desirable for identification of increased risk of severe toxicity.

DPYD; 5-FU; toxicity

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Podaci o prilogu

2013.

objavljeno

Podaci o matičnoj publikaciji

Pharmacogenomics and Theranostics in practice

Podaci o skupu

EUROMEDLAB Milano 2013 - Post-Congress Satellite Meetings Florence: Pharmacogenomics and Theranostics in practice

poster

24.05.2013-24.05.2013

Firenca, Italija

Povezanost rada

Kliničke medicinske znanosti