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Clinical Significance of UDP-Glucuronosyltransferase 1A1*6 for Toxicities of Combination Chemotherapy with Irinotecan and Cisplatin in Gynecologic Cancers

Authors :
Masashi Takano
Harushige Yokota
Michiko Takahashi
Tsunekazu Kita
Naoki Sasaki
Nao Kino
Tomoyuki Yoshikawa
Keiichi Fujiwara
Kenichi Furuya
Tomoko Goto
Koji Horie
Yoshihiro Kikuchi
Masafumi Kato
Kenji Ishii
Junko Hirata
Source :
Oncology. 76:315-321
Publication Year :
2009
Publisher :
S. Karger AG, 2009.

Abstract

Background: To investigate the effects of UDP-glucuronosyltransferase 1A1 (UGT1A1) *28, *6 and *27 in patients with gynecologic cancer who received chemotherapy with irinotecan and cisplatin. Methods: Patients eligible for this study had cervical or ovarian cancer treated with chemotherapy; a course of the regimen consisted of 60 mg/m2 of irinotecan on days 1, 8 and 15, and 60 mg/m2 of cisplatin on day 1 every 4 weeks. UGT1A1 polymorphisms and toxicities were analyzed. Results: From March 2007 to December 2007, 30 Japanese patients were enrolled; 24 ovarian carcinoma patients and 6 cervical cancer patients. The following genotypes of UGT1A1 were found: wild type in 17 patients (57%), *28 in 4 patients (13%), *6 in 8 patients (27%), *28*6 in 1 case (3%) and no case of *27 (0%). Grade 3/4 neutropenia, thrombocytopenia and diarrhea were significantly more frequent in *6 patients compared with wild-type patients. Also, in *6 patients irinotecan administration on days 8 or 15 was significantly more often omitted due to toxicities. In patients with *28 or *28*6, side effects were similar to those in patients with *6. Conclusion: In addition to UGT1A1*28, UGT1A1*6 might also be a key candidate to determine the dose of combination chemotherapy with irinotecan and cisplatin.

Details

ISSN :
14230232 and 00302414
Volume :
76
Database :
OpenAIRE
Journal :
Oncology
Accession number :
edsair.doi...........81360472297ab04522a2809e1151f11f
Full Text :
https://doi.org/10.1159/000209335