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:34
|
作者
Nakamae, Hirohisa [1 ]
Fujisawa, Shin [2 ]
Ogura, Michinori [3 ,4 ]
Uchida, Toshiki [3 ]
Onishi, Yasushi [5 ]
Taniwaki, Masafumi [6 ]
Utsunomiya, Atae [7 ]
Matsue, Kosei [8 ]
Takamatsu, Yasushi [9 ]
Usuki, Kensuke [10 ]
Tanimoto, Mitsune [11 ]
Ishida, Yoji [12 ]
Ohashi, Kazuteru [13 ]
Li, Li [14 ]
Miyoshi, Masafumi [15 ]
机构
[1] Osaka City Univ, Grad Sch Med, Dept Hematol, Abeno Ku, 1-4-3 Asahi Machi, Osaka 5458585, Japan
[2] Yokohama City Univ, Dept Hematol, Med Ctr, Yokohama, Kanagawa, Japan
[3] Japanese Red Cross Nagoya Daini Hosp, Dept Hematol & Oncol, Nagoya, Aichi, Japan
[4] Tokai Cent Hosp, Dept Hematol, Gifu, Japan
[5] Tohoku Univ Hosp, Dept Hematol & Rheumatol, Sendai, Miyagi, Japan
[6] Kyoto Prefectural Univ Med, Univ Hosp, Dept Hematol, Kyoto, Japan
[7] Imamura Bun In Hosp, Dept Hematol, Kagoshima, Japan
[8] Kameda Med Ctr, Dept Internal Med, Chiba, Japan
[9] Fukuoka Univ Hosp, Div Med Oncol Hematol & Infect Dis, Dept Internal Med, Fukuoka, Japan
[10] NTT Med Ctr Tokyo, Dept Hematol, Tokyo, Japan
[11] Okayama Univ Hosp, Dept Hematol & Oncol, Okayama, Japan
[12] Iwate Med Univ, Dept Hematol & Oncol, Internal Med, Sch Med, Morioka, Iwate, Japan
[13] Tokyo Metropolitan Komagome Hosp, Canc & Infect Dis Ctr, Tokyo, Japan
[14] Bristol Myers Squibb, Princeton, NJ USA
[15] Bristol Myers Squibb, Tokyo, Japan
关键词
CML; Tyrosine kinase inhibitor; Dasatinib; Imatinib; Japan; MOLECULAR RESPONSE; FOLLOW-UP; INTERFERON; TRIAL; SURVIVAL; EFFICACY; THERAPY; SAFETY;
D O I
10.1007/s12185-017-2208-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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 ae<currency>0.0032% International Scale [MR4.5]: 58 vs 52%). In patients who achieved BCR-ABL1 ae<currency>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.
引用
收藏
页码:792 / 804
页数:13
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