In vitro Activity of Bcr-Abl Inhibitors AMN107 and BMS-354825 against Clinically Relevant Imatinib-Resistant Abl Kinase Domain Mutants
Howard Hughes Medical Institute · Oregon Health & Science University · +5 more institutions
Abstract
Imatinib, a Bcr-Abl tyrosine kinase inhibitor, is a highly effective therapy for patients with chronic myelogenous leukemia (CML). Despite durable responses in most chronic phase patients, relapses have been observed and are much more prevalent in patients with advanced disease. The most common mechanism of acquired imatinib resistance has been traced to Bcr-Abl kinase domain mutations with decreased imatinib sensitivity. Thus, alternate Bcr-Abl kinase inhibitors that have activity against imatinib-resistant mutants would be useful for patients who relapse on imatinib therapy. Two such Bcr-Abl inhibitors are currently being evaluated in clinical trials: the improved potency, selective Abl inhibitor AMN107 and…
Citation impact
- FWCI
- 39.86
- Percentile
- 100%
- References
- 24
Authors
11Topics & keywords
- Imatinib
- Tyrosine kinase
- Chronic myelogenous leukemia
- Nilotinib
- ABL
- Cancer research
- Tyrosine-kinase inhibitor
- Protein kinase domain