Pregled bibliografske jedinice broj: 1271853
DPYD polymorphism c.496A>G and risk of severe adverse drug reactions in cancer patients treated with fluoropyrimidine-based protocols
DPYD polymorphism c.496A>G and risk of severe adverse drug reactions in cancer patients treated with fluoropyrimidine-based protocols // 8th European virtual congress of pharmacology (EPHAR 2021): From Great Science to better Medicine for Europe
online, 2021. str. /-/ (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1271853 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
DPYD polymorphism c.496A>G and risk of severe
adverse drug reactions in cancer patients treated
with fluoropyrimidine-based protocols
Autori
Ganoci, L. ; Bilić, I. ; Trkulja, V. ; Lešnjaković, L. ; Šimićević, L. ; Mucalo, I. ; pleština, S. ; Božina, N.
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
8th European virtual congress of pharmacology (EPHAR 2021): From Great Science to better Medicine for Europe
Mjesto i datum
Online, 06.12.2021. - 08.12.2021
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
drugs reaction ; cancer ; fluoropyrimidine
Sažetak
Patients with reduced dihydropyrimidine dehydrogenase (DPD) activity are at increased risk of severe fluoropyrimidine (FP)- related adverse events (AE). Several guidelines recommend FP dosing based on genotyping of four clinically relevant DPYD variants to predict DPD activity. We investigated the relationship between three further DPYD polymorphisms and the risk of severe FP-related AES. Study involved FP-treated cancer patients, genotyped for recommended DPYD variants 2A. *13 (c.1679T G). c.2846A T. c.1236G>A/HapB3. as well for c.496A G. c.2194G>A and c.85T>C (TaqMan real-time PCR) and for UGT1A1*28 (LightSNIP) if irinotecan was included. Patients were monitored for occurrence of grade 23 (National Cancer Institute Common Terminology Criteria) vs. grade 0-2 AES. For each tested polymorphisms, variant allele carriers were matched to respective wild type controls. Of 503 included patients (82.3% colorectal cancer), 283 (56.3%) developed grade 23 AES. Odds of grade 23 AEs were higher in c.496A G variant allele carriers (n=127) than in controls (n-376) [OR-5.20 (95%CI 1.88-14.3). Bayesian OR-5, 24 (95% Cri 3.06- 9.12)]. Odds tended to be higher in c.2194G>A variant allele carries (n=58) than in controls (n=432) (OR=1.88 (0.95-3.73), Bayesian OR=1.90 (1.03.3.56), c.8ST-G variant did not appear associated with grade 23 AES. DRYD C496ADG variant might need to be considered for inclusion in the DPYD genotyping pariel.
Izvorni jezik
Engleski
Znanstvena područja
Farmacija
POVEZANOST RADA
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb
Profili:
LIVIJA ŠIMIČEVIĆ
(autor)
Stjepko Pleština
(autor)
Iva Mucalo
(autor)
Lana Ganoci
(autor)
Nada Božina
(autor)
Lucija Lešnjaković
(autor)
Vladimir Trkulja
(autor)