Dasatinib versus imatinib in Japanese patients with newly diagnosed chronic phase chronic myeloid leukemia: a subanalysis of the DASISION 5-year final report

被引:0
作者
Hirohisa Nakamae
Shin Fujisawa
Michinori Ogura
Toshiki Uchida
Yasushi Onishi
Masafumi Taniwaki
Atae Utsunomiya
Kosei Matsue
Yasushi Takamatsu
Kensuke Usuki
Mitsune Tanimoto
Yoji Ishida
Kazuteru Ohashi
Li Li
Masafumi Miyoshi
机构
[1] Osaka City University,Department of Hematology, Graduate School of Medicine
[2] Yokohama City University Medical Center,Department of Hematology
[3] Japanese Red Cross Nagoya Daini Hospital,Department of Hematology and Oncology
[4] Tokai Central Hospital,Department of Hematology
[5] Tohoku University Hospital,Department of Hematology and Rheumatology
[6] Kyoto Prefectural University of Medicine,Department of Hematology, University Hospital
[7] Imamura Bun-in Hospital,Department of Hematology
[8] Kameda Medical Center,Department of Internal Medicine
[9] Fukuoka University Hospital,Division of Medical Oncology, Hematology and Infectious Diseases, Department of Internal Medicine
[10] NTT Medical Center Tokyo,Department of Hematology
[11] Okayama University Hospital,Department of Hematology and Oncology
[12] Iwate Medical University School of Medicine,Department of Hematology and Oncology, Internal Medicine
[13] Tokyo Metropolitan Komagome Hospital,Cancer and Infectious Diseases Center
[14] Bristol-Myers Squibb,undefined
[15] Bristol-Myers Squibb,undefined
来源
International Journal of Hematology | 2017年 / 105卷
关键词
CML; Tyrosine kinase inhibitor; Dasatinib; Imatinib; Japan;
D O I
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摘要
The international phase III DASISION trial demonstrated improved efficacy of dasatinib versus imatinib in treatment-naive patients with chronic myeloid leukemia in the chronic phase (CML-CP). We report efficacy and safety outcomes in a Japanese population from the final, 5-year follow-up of DASISION. At the end of the study, 77% (20/26) of dasatinib-treated and 61% (14/23) of imatinib-treated patients remained on initial therapy. Improved responses were observed in Japanese patients who received dasatinib versus imatinib (complete cytogenetic response: 96 vs 87%; major molecular response: 88 vs 74%; BCR-ABL1 ≤0.0032% International Scale [MR4.5]: 58 vs 52%). In patients who achieved BCR-ABL1 ≤10% at 3 months, 5-year progression-free survival and overall survival rates were high with dasatinib (96 and 96%) and imatinib (88 and 100%). The majority of adverse events were grade 1/2 in Japanese patients. Pleural effusion occurred more frequently in dasatinib-treated Japanese patients versus all patients (42 vs 28%), with no treatment discontinuations. Overall, in Japanese patients, dasatinib maintained its safety profile and had higher or comparable response and survival outcomes compared with imatinib or with all patients in DASISION. These findings demonstrate the long-term efficacy and tolerability of dasatinib and support frontline treatment of Japanese patients with CML-CP with dasatinib.
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页码:792 / 804
页数:12
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