2018
The significance of enzyme and transporter polymorphisms for imatinib plasma levels and achieving an optimal response in chronic myeloid leukemia patients
BELOHLAVKOVA, Petra, Filip VRBACKY, Jaroslava VOGLOVA, Zdeněk RÁČIL, Daniela ŽÁČKOVÁ et. al.Základní údaje
Originální název
The significance of enzyme and transporter polymorphisms for imatinib plasma levels and achieving an optimal response in chronic myeloid leukemia patients
Autoři
BELOHLAVKOVA, Petra (203 Česká republika, garant), Filip VRBACKY (203 Česká republika), Jaroslava VOGLOVA (203 Česká republika), Zdeněk RÁČIL (203 Česká republika, domácí), Daniela ŽÁČKOVÁ (203 Česká republika, domácí), Katerina HROCHOVA (203 Česká republika), Jana MALAKOVA (203 Česká republika), Jiří MAYER (203 Česká republika, domácí) a Pavel ZAK (203 Česká republika)
Vydání
Archives of Medical Science, Poland, Termedia Publishing House, 2018, 1734-1922
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30204 Oncology
Stát vydavatele
Polsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.380
Kód RIV
RIV/00216224:14110/18:00105953
Organizační jednotka
Lékařská fakulta
UT WoS
000448045000023
Klíčová slova anglicky
clinical response; imatinib; chronic myeloid leukemia; genetic polymorphisms
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 11. 2. 2019 14:21, Soňa Böhmová
Anotace
V originále
Introduction: Imatinib mesylate is the drug of choice for patients with chronic myeloid leukemia (CML). Imatinib pharmacokinetics is affected by a number of transport proteins and enzymes. Material and methods: In the present study we evaluated the association of eight polymorphisms in the seven genes CYP3A5*3 (rs776746), CYP3A4*1 (rs2740574), CYP2C9*3 (rs1057910), SLC22A1 (rs683369), ABCB1 (rs1045642, rs1128503), ABCG2 (rs2231142) and ABCC2 (rs717620) with imatinib plasma level and achieving an optimal clinical response in 112 CML patients (53 men and 59 women). Results: No association was found between the examined polymorphisms in rs776746, rs2740574, rs1057910, rs683369, rs1045642, rs1128503, rs2231142, rs717620 and the achieved imatinib plasma level. The influence of rs776746 (CYP3A5*3) on the achievement of a complete cytogenetic response (CCyR) at 6 months was borderline non-significant (p = 0.06). Furthermore, no association was demonstrated between rs776746 polymorphisms and the achievement of a major molecular response (MMR) at 12 or 18 months. Polymorphisms rs776746, rs2740574, rs1057910, rs683369, rs1045642, rs1128503, rs2231142, rs717620 showed no impact on the optimal therapeutic response. Conclusions: Despite the results of some other studies, no other polymorphism we analyzed was associated with imatinib plasma level or clinical response. The treatment outcomes cannot be predicted using the candidate gene approach and treatment decisions cannot be made according to the polymorphisms investigated in this study.