Abstract |
Recent pharmacogenetic studies on irinotecan have revealed the impact of UDP glucuronosyltransferase (UGT) 1A1*28 on severe irinotecan toxicities. Although the clinical role of UGT1A1*6, which is specifically detected in East Asian patients, in irinotecan toxicities is suggested, clear evidence remains limited. To examine the impact of *6, the association of UGT1A1 genotypes with severe irinotecan toxicities was retrospectively investigated in Japanese cancer patients. A significant *6-dependent increase in the incidence of grade 3 or 4 neutropenia was observed in 49 patients on irinotecan monotherapy (p=0.012). This study further clarifies the clinical importance of *6 in irinotecan therapy in East Asians.
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Authors | Kimie Sai, Yoshiro Saito, Hiromi Sakamoto, Kuniaki Shirao, Koichi Kurose, Mayumi Saeki, Shogo Ozawa, Nahoko Kaniwa, Setsuo Hirohashi, Nagahiro Saijo, Jun-ichi Sawada, Teruhiko Yoshida |
Journal | Cancer letters
(Cancer Lett)
Vol. 261
Issue 2
Pg. 165-71
(Mar 18 2008)
ISSN: 0304-3835 [Print] Ireland |
PMID | 18082937
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents, Phytogenic
- Irinotecan
- UGT1A1 enzyme
- Glucuronosyltransferase
- Bilirubin
- Camptothecin
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Topics |
- Adult
- Aged
- Antineoplastic Agents, Phytogenic
(adverse effects)
- Asian People
(genetics)
- Bilirubin
(blood)
- Camptothecin
(adverse effects, analogs & derivatives)
- Female
- Genotype
- Glucuronosyltransferase
(genetics, metabolism)
- Humans
- Incidence
- Irinotecan
- Japan
(epidemiology)
- Male
- Middle Aged
- Neoplasms
(drug therapy, genetics, pathology)
- Polymorphism, Genetic
- Retrospective Studies
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