Dasatinib in the Treatment of Chronic Myeloid Leukemia in Accelerated Phase After Imatinib Failure: The START A Trial

Author:

Apperley Jane F.1,Cortes Jorge E.1,Kim Dong-Wook1,Roy Lydia1,Roboz Gail J.1,Rosti Gianantonio1,Bullorsky Eduardo O.1,Abruzzese Elisabetta1,Hochhaus Andreas1,Heim Dominik1,de Souza Carmino A.1,Larson Richard A.1,Lipton Jeffrey H.1,Khoury H. Jean1,Kim Hyeoung-Joon1,Sillaber Christian1,Hughes Timothy P.1,Erben Philipp1,Van Tornout Jan1,Stone Richard M.1

Affiliation:

1. From the Hammersmith Hospital, Imperial College, London, United Kingdom; The University of Texas M. D. Anderson Cancer Center, Houston, TX; St Mary's Hospital, the Catholic University of Korea, Seoul; Chonnam National University, Hwasun-gun, Jeollanam-do, Korea; Clinical Research Center, Centre Hospitalier Universitaire de Poitiers, Poitiers, France; Weill Medical College of Cornell University, New York Presbyterian Hospital, New York, NY; S Orsola-Malpighi University Hospital, Bologna; Ospedale S....

Abstract

PurposePatients with chronic myelogenous leukemia in accelerated phase (CML-AP) that is resistant or intolerant to imatinib have limited therapeutic options. Dasatinib, a potent inhibitor of BCR-ABL and SRC-family kinases, has efficacy in patients with CML-AP who have experienced treatment failure with imatinib. We now report follow-up data from the full patient cohort of 174 patients enrolled onto a phase II trial to provide a more complete assessment of the efficacy and safety of dasatinib in this population.Patients and MethodsPatients with imatinib-resistant (n = 161) or -intolerant (n = 13) CML-AP received dasatinib 70 mg orally twice daily.ResultsAt a median follow-up of 14.1 months (treatment duration, 0.1 to 21.7 months), major and complete hematologic responses were attained by 64% and 45% of patients, respectively, and major and complete cytogenetic responses were achieved in 39% and 32% of patients, respectively. Responses were achieved irrespective of imatinib status (resistant or intolerant), prior stem-cell transplantation, or the presence of prior BCR-ABL mutation. The 12-month progression-free survival and overall survival rates were 66% and 82%, respectively. Dasatinib was generally well tolerated; the most frequent nonhematologic severe treatment-related adverse event was diarrhea (52%; grade 3 to 4, 8%). Cytopenias were common, including grade 3 to 4 neutropenia (76%) and thrombocytopenia (82%). Pleural effusion occurred in 27% of patients (grade 3 to 4, 5%).ConclusionDasatinib is effective in patients with CML-AP after imatinib treatment failure.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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