Dasatinib is an orally available multikinase inhibitor indicated for the treatment of Philadelphia chromosome (Ph)-positive leukemias. Ph is a chromosomal abnormality found in patients with chronic myelogenous leukemia (CML) and acute lymphocytic leukemia (ALL), where the ABL tyrosine kinase and the breakpoint cluster region (BCR) gene transcribe the chimeric protein BCR-ABL. BCR-ABL is associated with the uncontrolled activity of the ABL tyrosine kinase and is involved in the pathogenesis of CML and 15-30% of ALL cases. Dasatinib also inhibits a spectrum of kinases involved in cancer, including several SRC-family kinases.
Unlike imatinib, another tyrosine kinase used for the treatment of CML and Ph-positive ALL, dasatinib inhibits the active and inactive conformations of the ABL kinase domain. Also, mutations in the kinase domain of BCR-ABL may lead to relapse during imatinib treatment. Since dasatinib does not interact with some of the residues involved in those mutations, the use of this drug represents a therapeutic alternative for patients with cancers that have developed imatinib-resistance. The use of dasatinib was first approved by the FDA in 2006.
Dasatinib is indicated for the treatment of newly diagnosed adults with Philadelphia chromosome-positive (Ph+) chronic myeloid leukemia (CML) in chronic phase, as well as adults with chronic, accelerated, or myeloid or lymphoid blast phase Ph+ CML with resistance or intolerance to prior therapy including imatinib, and adults with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) with resistance or intolerance to prior therapy. Dasatinib is also indicated for the treatment of pediatric patients 1 year of age and older with Ph+ CML in chronic phase or newly diagnosed Ph+ ALL in combination with chemotherapy.
Winship Cancer Institute, Emory University, Atlanta, Georgia, United States
Orlando Health, Inc. M.D. Anderson Cancer Center Orlando, Orlando, Florida, United States
Local Institution, Salamanca, Spain
University of Nebraska Medical Center, Internal Medicine Section of Oncology/Hematology, Omaha, Nebraska, United States
Palm Beach Cancer Center Institute, West Palm Beach, Florida, United States
Duke University Medical Center, Durham, North Carolina, United States
Presbyterian Health Care, Charlotte, North Carolina, United States
City of Hope Comprehensive Cancer Center, Duarte, California, United States
City of Hope Medical Group, Pasadena, California, United States
Weill Cornell Medical College - New York Presbyterian Hospital, New York, New York, United States
Emory Winship Cancer Institute, Atlanta, Georgia, United States
The Jones Clinic, Germantown, Tennessee, United States
Local Institution - 0004, Fuzhou, Fujian, China
Local Institution - 0008, Suzhou, Jiangsu, China
Local Institution, Hangzhou, Zhejiang, China
Memorial Hospital of South Bend, South Bend, Indiana, United States
Center for Cancer Therapy at LaPorte Hospital and Health Services, La Porte, Indiana, United States
Rebecca and John Moores UCSD Cancer Center, La Jolla, California, United States
M D Anderson Cancer Center, Houston, Texas, United States
University of Chicago, Chicago, Illinois, United States
University of Texas MD Anderson Cancer Center, Houston, Texas, United States
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.