TY - JOUR
T1 - Efficacy and safety of dasatinib versus imatinib in Japanese patients with newly diagnosed chronic-phase chronic myeloid leukemia (CML-CP)
T2 - Subset analysis of the DASISION trial with 2-year follow-up.
AU - Fujisawa, Shin
AU - Nakamae, Hirohisa
AU - Ogura, Michinori
AU - Ishizawa, Ken ichi
AU - Taniwaki, Masafumi
AU - Utsunomiya, Atae
AU - Matsue, Kosei
AU - Takamatsu, Yasushi
AU - Usuki, Kensuke
AU - Tanimoto, Mitsune
AU - Ishida, Yoji
AU - Akiyama, Hideki
AU - Onishi, Shintaro
N1 - Funding Information:
Conflict of interest Shin Fujisawa has no conflict of interest to disclose. Hirohisa Nakamae has served as a consultant and lecturer for Novartis and Bristol-Myers Squibb and received from both: grants and payment for travel/accommodations/meeting expenses unrelated to activities listed. Michinori Ogura has received research funding from Bristol-Myers Squibb, Eisai, Kyowa Hakko Kirin Co., Ltd, Chugai, Pfizer, Novartis, Solasia, Celgene, SymBio, GlaxoSmithK-line, Otsuka, Dainippon Sumitomo, MSD, and Janssen Pharma. Ken-ichi Ishizawa has no conflict of interest to disclose. Masafumi Tani-waki has no conflict of interest to disclose. Atae Utsunomiya has received consulting fees or honorarium from Bristol-Myers K.K. and Kyowa Hakko Kirin Co., Ltd. Kosei Matsue has no conflict of interest to disclose. Yasushi Takamatsu has no conflict of interest to disclose. Kensuke Usuki has no conflict of interest to disclose. Mitsune Tan-imoto has no conflict of interest to disclose. Yoji Ishida has no conflict of interest to disclose. Hideki Akiyama has no conflict of interest to disclose. Shintaro Onishi is employed by Otsuka, and was formerly employed by Bristol-Myers Squibb throughout the manuscript development.
Funding Information:
Acknowledgments The authors would like to thank all participating study sites for this Bristol-Myers Squibb-sponsored study. The authors would like to particularly thank the patients who participated in this study and acknowledge the efforts of study staff at the study centers in Japan: Osaka City University Hospital, Nagoya Daini Red Cross Hospital, Yokohama City University Medical Center, Tohoku University Hospital, University Hospital, Kyoto Prefectural University of Medicine, Imamura Bun-in Hospital, Kameda Clinic of Medical Corporation Tesshokai, Fukuoka University Hospital, Kanto Medical Center NTT EC, Okayama University Hospital, Iwate Medical University Hospital, and Tokyo Metropolitan Komagome Hospital. StemScientific, funded by Bristol-Myers Squibb, provided writing and editorial support. The authors did not receive financial compensation for authoring the manuscript.
PY - 2014/2
Y1 - 2014/2
N2 - Dasatinib is a highly potent BCR-ABL kinase inhibitor with established efficacy and safety in imatinib-resistant or -intolerant patients with chronic myeloid leukemia (CML) and Philadelphia chromosome-positive acute lymphoblastic leukemia. In the global phase III DASISION trial in patients with newly diagnosed chronic phase CML (CML-CP), dasatinib was found to have an acceptable safety profile and demonstrated significantly faster and higher rates of complete cytogenetic response (CCyR) and major molecular response (MMR) compared with imatinib. Here, we report the results of a subset analysis of Japanese patients enrolled in the DASISION trial, showing safety and efficacy profiles generally consistent with patients enrolled worldwide, including higher response rates (CCyR, MMR) with dasatinib compared with imatinib and similar high rates of progression-free and overall survival with both therapies. However, the small sample size of the present study limits the strength of these conclusions, and further exploration is needed to confirm any differences observed in Japanese patients compared with the total treated population. These findings support the use of dasatinib 100 mg QD as a first-line treatment in Japanese patients with newly diagnosed CML-CP.
AB - Dasatinib is a highly potent BCR-ABL kinase inhibitor with established efficacy and safety in imatinib-resistant or -intolerant patients with chronic myeloid leukemia (CML) and Philadelphia chromosome-positive acute lymphoblastic leukemia. In the global phase III DASISION trial in patients with newly diagnosed chronic phase CML (CML-CP), dasatinib was found to have an acceptable safety profile and demonstrated significantly faster and higher rates of complete cytogenetic response (CCyR) and major molecular response (MMR) compared with imatinib. Here, we report the results of a subset analysis of Japanese patients enrolled in the DASISION trial, showing safety and efficacy profiles generally consistent with patients enrolled worldwide, including higher response rates (CCyR, MMR) with dasatinib compared with imatinib and similar high rates of progression-free and overall survival with both therapies. However, the small sample size of the present study limits the strength of these conclusions, and further exploration is needed to confirm any differences observed in Japanese patients compared with the total treated population. These findings support the use of dasatinib 100 mg QD as a first-line treatment in Japanese patients with newly diagnosed CML-CP.
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U2 - 10.1007/s12185-013-1470-1
DO - 10.1007/s12185-013-1470-1
M3 - Article
C2 - 24357015
AN - SCOPUS:84906929521
SN - 0925-5710
VL - 99
SP - 141
EP - 153
JO - International Journal of Hematology
JF - International Journal of Hematology
IS - 2
ER -