Back to Search
Start Over
Dasatinib, large granular lymphocytosis, and pleural effusion: useful or adverse effect?
- Source :
-
Critical reviews in oncology/hematology [Crit Rev Oncol Hematol] 2014 Feb; Vol. 89 (2), pp. 242-7. Date of Electronic Publication: 2013 Oct 12. - Publication Year :
- 2014
-
Abstract
- Dasatinib is a second generation tyrosine kinase inhibitor approved for clinical use in first line and imatinib-resistant chronic myeloid leukemia and Philadelphia positive (Ph+) acute lymphoblastic leukemia. In addition to BCR-ABL1, dasatinib inhibits TEC kinases and SRC family kinases and is more potent than imatinib in the treatment of Ph+ leukemias. In the last 3 years, increases in cytotoxic T and natural-killer cells in peripheral blood samples have been reported in cases treated by dasatinib. The awareness of the clonal expansion of large granular lymphocytes and beneficial effect of these clonal cells increased the interest to dasatinib in cases receiving this drug. Clonal expansion of large granular lymphocytes is an important effect of dasatinib therapy, shown to be an off-target phenomenon associated with pleural effusion and better clinical response. The benefit of dasatinib-induced lymphocytosis and its underlying mechanism of this are important points for clinicians working in hematology and oncology.<br /> (Copyright © 2013 Elsevier Ireland Ltd. All rights reserved.)
- Subjects :
- Animals
Dasatinib
Humans
Leukemia, Myelogenous, Chronic, BCR-ABL Positive drug therapy
Lymphocytosis chemically induced
Pleural Effusion chemically induced
Protein Kinase Inhibitors adverse effects
Protein Kinase Inhibitors therapeutic use
Pyrimidines adverse effects
Pyrimidines therapeutic use
Thiazoles adverse effects
Thiazoles therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0461
- Volume :
- 89
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Critical reviews in oncology/hematology
- Publication Type :
- Academic Journal
- Accession number :
- 24210599
- Full Text :
- https://doi.org/10.1016/j.critrevonc.2013.10.005