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Correlation of UGT1A1(*)28 and (*)6 polymorphisms with irinotecan-induced neutropenia in Thai colorectal cancer patients.

Authors :
Atasilp C
Chansriwong P
Sirachainan E
Reungwetwattana T
Chamnanphon M
Puangpetch A
Wongwaisayawan S
Sukasem C
Source :
Drug metabolism and pharmacokinetics [Drug Metab Pharmacokinet] 2016 Feb; Vol. 31 (1), pp. 90-94. Date of Electronic Publication: 2015 Dec 31.
Publication Year :
2016

Abstract

UDP-glucuronosyltransferase1A1 (UGT1A1) polymorphisms have been related with irinotecan toxicity. The purpose of this study was to determine the associations between UGT1A1(*)28 and (*)6 polymorphisms and irinotecan toxicity in Thai patients with metastatic colorectal cancer. 44 metastatic colorectal cancer patients received irinotecan-based chemotherapy. Hematologic toxicities were determined in the first and second cycles of treatment. The genotypes of UGT1A1(*)28 and (*)6 were analyzed by pyrosequencing technique. The frequencies of genetic testing for UGT1A1(*)28 and (*)6 polymorphisms were 22.8% (TA6/TA7; 20.5%, TA7/TA7; 2.3%) and 15.9% (GA), respectively. No patients had the homozygous UGT1A1(*)6 (AA). Neither UGT1A1(*)28 nor UGT1A1(*)6 polymorphisms were significantly associated with severe hematologic toxicities. However, analysis of UGT1A1(*)28 and (*)6 in combination revealed an association with severe neutropenia in the first and second cycles (P = 0.044, P = 0.017, respectively). Both UGT1A1(*)28 and (*)6 polymorphisms may have an increased risk of irinotecan-induced neutropenia in Thai colorectal cancer patients.<br /> (Copyright © 2015 The Japanese Society for the Study of Xenobiotics. Published by Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1880-0920
Volume :
31
Issue :
1
Database :
MEDLINE
Journal :
Drug metabolism and pharmacokinetics
Publication Type :
Academic Journal
Accession number :
26830078
Full Text :
https://doi.org/10.1016/j.dmpk.2015.12.004