Simplifying procedure for prediction of resistance risk in CML patients - Test of sensitivity to TKI ex vivo
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
27067491
DOI
10.1016/j.bcmd.2016.03.005
PII: S1079-9796(16)30019-5
Knihovny.cz E-resources
- Keywords
- Chronic myeloid leukemia, Early predictors, Resistance,
- MeSH
- Antineoplastic Agents pharmacology therapeutic use MeSH
- Cell Death drug effects MeSH
- Drug Resistance, Neoplasm * MeSH
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive drug therapy pathology MeSH
- Dasatinib pharmacology therapeutic use MeSH
- Imatinib Mesylate pharmacology therapeutic use MeSH
- Protein Kinase Inhibitors pharmacology therapeutic use MeSH
- Leukocytes drug effects pathology MeSH
- Humans MeSH
- Cell Line, Tumor MeSH
- Pyrimidines pharmacology therapeutic use MeSH
- Cell Survival drug effects MeSH
- Treatment Outcome MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Antineoplastic Agents MeSH
- Dasatinib MeSH
- Imatinib Mesylate MeSH
- Protein Kinase Inhibitors MeSH
- nilotinib MeSH Browser
- Pyrimidines MeSH
Tyrosine kinase inhibitors (TKIs) targeting BCR-ABL have dramatically improved chronic myeloid leukemia therapy. While imatinib remains to be the first line therapy, about 30% of patients develop resistance or intolerance to this drug and are recommended to switch to other TKIs. Nilotinib and dasatinib are currently implemented into the first line therapy and other inhibitors have already entered the clinical practice. This opens further questions on how to select the best TKI for each patient not only during the therapy but also at diagnosis. The individualized therapy concept requires a reliable establishment of prognosis and prediction of response to the available TKIs. We tested the ex vivo sensitivity of patient primary leukocytes to imatinib, nilotinib and dasatinib - two concentrations of each inhibitor for 48h incubation - and we evaluated the usefulness of such tests for the clinical practice. Besides reflecting the actual sensitivity to the therapy, our optimized simple tests were able to predict the outcome in 90/87% of patients, for the next 12/24months, respectively. According to these results, the presented ex vivo testing could help clinicians to select the appropriate drug for each patient at diagnosis and also at any time of the therapy.
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