Imatinib trough plasma levels do not correlate with the response to therapy in patients with chronic myeloid leukemia in routine clinical setting
Language English Country Germany Media print-electronic
Document type Evaluation Study, Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Benzamides MeSH
- Blood Chemical Analysis MeSH
- Biomarkers, Pharmacological analysis blood MeSH
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive blood diagnosis drug therapy metabolism MeSH
- Diagnostic Tests, Routine MeSH
- Adult MeSH
- Imatinib Mesylate MeSH
- Clinical Laboratory Techniques MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Piperazines analysis blood pharmacokinetics therapeutic use MeSH
- Predictive Value of Tests MeSH
- Prognosis MeSH
- Antineoplastic Agents analysis blood pharmacokinetics therapeutic use MeSH
- Pyrimidines analysis blood pharmacokinetics therapeutic use MeSH
- Retrospective Studies MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Evaluation Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Benzamides MeSH
- Biomarkers, Pharmacological MeSH
- Imatinib Mesylate MeSH
- Piperazines MeSH
- Antineoplastic Agents MeSH
- Pyrimidines MeSH
Association of trough imatinib plasma levels (IPL) with cytogenetic or molecular response to treatment in patients with chronic myeloid leukemia (CML) was repeatedly reported. We analyzed their value in the routine clinical setting in 131 patients with chronic phase CML in whom imatinib was applied as first- or second-line treatment. A total of 1,118 measurements were obtained by ultra-performance liquid chromatography-tandem mass spectrometry assay in patients treated with daily dose of imatinib ranging from 100 to 800 mg. Samples were obtained from 1 to 96 h after drug ingestion. High inter (36%) and intraindividual variability (9-33%) of IPL was observed. For analysis of correlation of IPL with treatment response, two sets of samples were selected according to the European LeukemiaNet (ELN) criteria. The first set consisted of 241 samples taken 24 ± 2 h after dosing in 54 patients, and the second one consisted of 329 samples taken 24 ± 4 h after imatinib ingestion in 84 patients. In both sets, only patients treated with 400 mg imatinib once daily for at least 18 months were included. From multiple measurements in individual patients, mean IPL were used. In both sets, we were not able to demonstrate a statistically significant correlation between IPL and response to treatment according to the ELN. We believe that this was due to the differences in patients' compliance, leukemia biology, and other variables that are difficult to eliminate in the routine clinical practice. The use of IPL for prognostic estimation in CML treatment outside the clinical trials is probably limited.
References provided by Crossref.org