| Literature DB >> 19266256 |
Mari Sakai1, Yasushi Miyazaki2, Emi Matsuo1, Yukiyoshi Moriuchi3, Tomoko Hata1, Takuya Fukushima1, Yoshitaka Imaizumi1, Daisuke Imanishi1, Jun Taguchi1, Masako Iwanaga1, Hideki Tsushima3, Yoriko Inoue3, Yumi Takasaki3, Takeshi Tsuchiya1, Minori Komoda1, Koji Ando1, Kensuke Horio1, Yuji Moriwaki3, Shinya Tominaga1, Hidehiro Itonaga1, Kazuhiro Nagai1, Kunihiro Tsukasaki1, Chizuko Tsutsumi3, Yasushi Sawayama3, Reishi Yamasaki3, Daisuke Ogawa3, Yasuhisa Kawaguchi3, Shuichi Ikeda3, Shinichiro Yoshida3, Yasuyuki Onimaru3, Masayuki Tawara3, Sunao Atogami3, Satoshi Koida3, Tatsuro Joh3, Masaomi Yamamura3, Yuji Matsuo3, Hisashi Soda3, Hiroaki Nonaka3, Itsuro Jinnai3, Kazutaka Kuriyama3, Masao Tomonaga1.
Abstract
Imatinib has dramatically improved long-term survival of chronic myelogenous leukemia (CML) patients. To analyze its efficacy in a practical setting, we registered most of CML patients in Nagasaki Prefecture of Japan. Of these, 73 patients received imatinib as an initial therapy. The overall survival rate of these patients was 88.7% at 6 years, and the cumulative complete cytogenetic response rate was 82.5% at 18 months. These results are comparable with the data of other reports including the IRIS study; however, the administered imatinib dose was smaller in our study than that in other reports. To address these discrepancies, we measured the trough concentration of imatinib among 35 patients. Although 39% of the patients were administered less than 400 mg/day, the trough level was comparable to those of previous reports. The trough level of imatinib showed a significant relationship with its efficacy, and was clearly related to dose of imatinib administrated and dose of imatinib divided by body surface area (BSA). Considering the smaller BSA of Japanese patients as compared to those of foreign origin, the results suggest that a lower dose of imatinib could maintain enough trough level and provided excellent results for the treatment of CML in our registry.Entities:
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Year: 2009 PMID: 19266256 DOI: 10.1007/s12185-009-0263-z
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490