Clinical Efficacy and Safety of First-Line Dasatinib Therapy and the Relevance of Velocity of BCR-ABL1 Transcript Decline for Achievement of Molecular Responses in Newly Diagnosed Chronic-Phase Chronic Myeloid Leukemia: Report from the Juntendo Yamanashi Cooperative Study Group

被引:8
作者
Takaku, Tomoiku [1 ]
Iriyama, Noriyoshi [2 ]
Mitsumori, Toru [3 ]
Sato, Eriko [4 ]
Gotoh, Akihiko [1 ]
Kirito, Keita [3 ]
Noguchi, Masaaki [5 ]
Koike, Michiaki [6 ]
Sakamoto, Junichi [7 ]
Oba, Koji [8 ]
Komatsu, Norio [1 ]
机构
[1] Juntendo Univ, Sch Med, Dept Hematol, Tokyo, Japan
[2] Nihon Univ, Sch Med, Dept Med, Div Hematol & Rheumatol, Tokyo, Japan
[3] Univ Yamanashi, Dept Hematol Oncol, Chou Ku, Tokyo, Japan
[4] Juntendo Univ, Nerima Hosp, Dept Hematol, Tokyo, Japan
[5] Juntendo Univ, Urayasu Hosp, Dept Hematol, Urayasu, Japan
[6] Juntendo Univ, Shizuoka Hosp, Dept Hematol, Izunokuni, Japan
[7] Tokai Cent Hosp, Kakamigahara, Japan
[8] Univ Tokyo, Grad Sch Med, Sch Publ Hlth, Dept Biostat, Tokyo, Japan
关键词
Dasatinib; Newly diagnosed chronic myeloid leukemia; Molecular response; Halving time; Lymphocytosis; CHRONIC MYELOGENOUS LEUKEMIA; KINASE INHIBITOR THERAPY; FOLLOW-UP; IMATINIB; CML; LYMPHOCYTOSIS; RECOMMENDATIONS; PREDICTOR; EXPANSION; DASISION;
D O I
10.1159/000481945
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The use of tyrosine kinase inhibitors led to an improvement in the prognoses of patients with chronic myeloid leukemia (CML). The aims of this study were to investigate the efficacy and safety of dasatinib in Japanese patients and to explore the factors that affect the achievement of molecular responses. Methods: The primary endpoint was a major molecular response (MMR) by 12 months. The halving time for BCR-ABL1 transcripts was calculated using transcript levels. Results: Thirty-two patients with chronic-phase CML (CML-CP) were enrolled and 30 received 100 mg dasatinib once daily. At 24 months of follow-up, 21 (72%) and 24 (83%) patients achieved an MMR by 12 and 24 months, respectively; the rates of a deep molecular response (DMR) by 12 and 24 months were 48 and 59%, respectively. A shorter halving time of BCR-ABL1 transcripts (<= 10.6 days) accurately predicted both an MMR and a DMR. The incidence of pleural effusion was 50%. Our study reconfirmed the efficacy and safety of dasatinib treatment in Japanese patients with newly diagnosed CML-CP. In addition, the usefulness of the halving time of BCR-ABL1 transcripts was validated. Conclusion: These data emphasize the significance of an early treatment response in achieving a DMR during dasatinib therapy. (C) 2017 S. Karger AG, Basel
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收藏
页码:85 / 91
页数:7
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