Pharmacokinetics of Dasatinib
Language English Country Czech Republic Media print
Document type Journal Article, Review
Grant support
SVV 260373
Univerzita Karlova v Praze
PubMed
31586504
DOI
10.14712/23362936.2019.10
PII: pmr_2019120020052
Knihovny.cz E-resources
- Keywords
- Dasatinib, Drug interaction, Pharmacokinetics, pH-dependent absorption,
- MeSH
- Drug Resistance, Neoplasm MeSH
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive drug therapy metabolism MeSH
- Dasatinib pharmacokinetics therapeutic use MeSH
- Protein Kinase Inhibitors pharmacokinetics therapeutic use MeSH
- Hydrogen-Ion Concentration MeSH
- Humans MeSH
- Cytochrome P-450 Enzyme System MeSH
- Gastric Acid MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Names of Substances
- Dasatinib MeSH
- Protein Kinase Inhibitors MeSH
- Cytochrome P-450 Enzyme System MeSH
Tyrosine kinase inhibitors have recently become an essential tool in management of chronic myeloid leukaemia (CML). Dasatinib, a representative of those drugs, acts by inhibiting key proteins included in CML development, predominantly Bcr-Abl and Src. Its advantage is that it shows activity in many cases where other agents bring no improvement due to resistance. Pharmacokinetics of dasatinib has specific characteristics that may play an important role in achieving sufficient exposure in patients. Therefore, the key pharmacokinetic properties are summarized in this report. For example, dasatinib absorption is significantly influenced by gastric pH and its modulation can be a source of serious interactions, as well as simultaneous administration of drugs affecting cytochrome P450.
References provided by Crossref.org