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Efficacy and Safety of Imatinib Mesylate for Patients in the First Chronic Phase of Chronic Myeloid Leukemia: Results of a Japanese Phase II Clinical Study
Authors:Yasuo Morishima  Michinori Ogura  Miki Nishimura  Fumiharu Yazaki  Masami Bessho  Hideaki Mizoguchi  Shigeru Chiba  Hisamaru Hirai  Tetsuzo Tauchi  Akio Urabe  Masatomo Takahashi  Kazunori Ohnishi  Toshiya Yokozawa  Nobuhiko Emi  Masami Hirano  Chihiro Shimazaki  Shinji Nakao  Yasukazu Kawai  Masahiro Fujimoto  Hirokuni Taguchi  Itsuro Jinnai  Ryuzo Ohno
Affiliation:Department of Hematology and Cell Therapy, Aichi Cancer Center Hospital, Nagoya, Japan. ymorisim@aichi-cc.jp
Abstract:
Imatinib mesylate is a relatively new drug that targets the BCR-ABL chimeric protein, the molecular basis of chronic myeloid leukemia (CML). A phase II clinical trial in 39 Japanese patients in the first chronic phase of CML was conducted with imatinib mesylate at a dose of 400 mg/day. Hematologic complete response was obtained in 92.3% of the patients, complete cytogenetic response (CR) was obtained in 43.6%, and major partial CR was obtained in 20.5% of the patients. Although 29 of 39 patients required an adjustment of dosing because of grade 3 or 4 adverse events, most of the events were reversible, and 25 of the 29 patients were able to resume therapy. Between day 15 and day 35, grade 3 or 4 neutropenia and/or leukocytopenia occurred in 13 patients, and grade 3 thrombocytopenia occurred in 5 patients. Overall, nonhematologic grade 3 adverse events occurred in 28.2% of the patients. These data support the use of imatinib mesylate as the treatment of choice for chronic-phase CML patients.
Keywords:Imatinib mesylate  Chronic myeloid leukemia  Phase II clinical study
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