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
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