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

被引:0
|
作者
A Hochhaus
M Baccarani
M Deininger
J F Apperley
J H Lipton
S L Goldberg
S Corm
N P Shah
F Cervantes
R T Silver
D Niederwieser
R M Stone
H Dombret
R A Larson
L Roy
T Hughes
M C Müller
R Ezzeddine
A M Countouriotis
H M Kantarjian
机构
[1] III Medizinische Klinik,Department of Hematology–Oncology ‘L and A Seràgnoli,’ S Orsola
[2] Medizinische Fakultät Mannheim,Malpighi Hospital
[3] Universität Heidelberg,Department of Haematology
[4] University of Bologna,Department of Medical Oncology and Hematology
[5] OHSU Cancer Institute,Division of Hematology/Oncology
[6] Oregon Health & Science University,Department of Hematology
[7] Hammersmith Hospital,Division of Hematology/Oncology
[8] Imperial College,Department of Hematology
[9] Princess Margaret Hospital,Department of Medical Oncology
[10] The Cancer Center,Department of Medicine
[11] Hackensack University Medical Center,Division of Hematology
[12] Service des Maladies du Sang,Department of Leukemia
[13] Hôpital Claude Huriez,undefined
[14] San Francisco School of Medicine,undefined
[15] University of California,undefined
[16] Hospital Clinic i Provincial,undefined
[17] New York Presbyterian Hospital,undefined
[18] Weill Medical College of Cornell University,undefined
[19] Oncology and Coagulation,undefined
[20] University of Leipzig,undefined
[21] Dana-Farber Cancer Institute,undefined
[22] Service Clinique des Maladies du Sang,undefined
[23] Hôpital Saint-Louis,undefined
[24] University of Chicago,undefined
[25] Clinical Research Center,undefined
[26] CHU de Poitiers,undefined
[27] Institute of Medical and Veterinary Science,undefined
[28] Bristol–Myers Squibb,undefined
[29] MD Anderson Cancer Center,undefined
来源
Leukemia | 2008年 / 22卷
关键词
dasatinib; imatinib; chronic myeloid leukemia;
D O I
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学科分类号
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.
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页码:1200 / 1206
页数:6
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