Dasatinib induces durable cytogenetic responses in patients with chronic myelogenous leukemia in chronic phase with resistance or intolerance to imatinib

被引:271
|
作者
Hochhaus, A. [1 ]
Baccarani, M. [2 ]
Deininger, M. [3 ]
Apperley, J. F. [4 ]
Lipton, J. H. [5 ]
Goldberg, S. L. [6 ]
Corm, S. [7 ]
Shah, N. P. [8 ]
Cervantes, F. [9 ]
Silver, R. T. [10 ]
Niederwieser, D. [11 ]
Stone, R. M. [12 ]
Dombret, H. [13 ]
Larson, R. A. [14 ]
Roy, L. [15 ]
Hughes, T. [16 ]
Mueller, M. C.
Ezzeddine, R. [17 ]
Countouriotis, A. M. [17 ]
Kantarjian, H. M. [18 ]
机构
[1] Univ Heidelberg, Med Fak Mannheim, Med Klin 3, Abt Fuer Leukaemieforsch, D-68167 Mannheim, Germany
[2] Univ Bologna, S Orsola Malpighi Hosp, Dept Hematol Oncol L&A Seragnoli, Bologna, Italy
[3] Oregon Hlth & Sci Univ, OHSU Canc Inst, Portland, OR 97201 USA
[4] Hammersmith Hosp, Imperial Coll, Dept Hematol, London, England
[5] Princess Margaret Hosp, Dept Med Oncol & Hematol, Toronto, ON M4X 1K9, Canada
[6] Hackensack Univ, Med Ctr, Ctr Canc, Hackensack, NJ USA
[7] Hop Claude Huriez, Serv Malad Sang, Lille, France
[8] Univ Calif San Francisco, San Francisco Sch Med, Div Hematol Oncol, San Francisco, CA 94143 USA
[9] Hosp Clin Barcelona, Dept Hematol, Barcelona, Spain
[10] Cornell Univ, New York Presbyterian Hosp, Weill Med Coll, Div Hematol Oncol, New York, NY 10021 USA
[11] Univ Leipzig, Dept Hematol Oncol & Coagulat, Leipzig, Germany
[12] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[13] Hop St Louis, Serv Clin Malad Sang, Paris, France
[14] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[15] CHU Poitiers, Clin Res Ctr, Poitiers, France
[16] Inst Med & Vet Sci, Div Hematol, Adelaide, SA 5000, Australia
[17] Bristol Myers Squibb Co, Wallingford, CT 06492 USA
[18] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
关键词
dasatinib; imatinib; chronic myeloid leukemia;
D O I
10.1038/leu.2008.84
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Dasatinib, a potent inhibitor of BCR-ABL in vitro, is effective for patients with chronic myelogenous leukemia (CML) resistant or intolerant to imatinib. To provide a more definitive assessment of dasatinib in chronic-phase (CP)-CML, we report extended follow-up of a phase II trial, presenting data for the entire patient cohort (N=387). Dasatinib (70 mg) twice daily was administered to patients with imatinib-resistant or -intolerant CP-CML. With median follow-up of 15.2 months (treatment duration, < 1-18.4 months), a complete hematologic response was attained or maintained in 91% of patients. A major cytogenetic response (MCyR) was attained or maintained by 59% (52% imatinib resistant and 80% imatinib intolerant); this was complete in 49% of patients (40% imatinib resistant and 75% imatinib intolerant). Of 230 patients achieving an MCyR, 7 experienced disease progression. Fifteen-month progression-free survival was 90% while overall survival was 96%. Grade 3/4 thrombocytopenia and neutropenia were reported in 48 and 49% of patients, respectively. Non-hematologic toxicity ( any grade) consisted primarily of diarrhea (37%), headache (32%), fatigue (31%), dyspnea (30%) and pleural effusion (27%). Pleural effusions were classified as grade 3 in 6% of reported events, with no incidence of grade 4. Dasatinib is associated with high response rates in patients with imatinib-resistant or -intolerant CP-CML.
引用
收藏
页码:1200 / 1206
页数:7
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