Imatinib has proved to be effective in the treatment of chronic myeloid leukemia, but plasma levels above 1,000 ng/mL must be achieved to optimize activity. Therapeutic drug monitoring of imatinib is useful for patients that do not present clinical response. There are several analytical methods to measure imatinib in biosamples, which are mainly based on liquid chromatography with mass spectrometric or diode array spectrophotometric detection. The former is preferred due to its lower cost and wider availability. The present manuscript presents a review of the clinical and analytical aspects of the therapeutic drug monitoring of imatinib in the treatment of chronic myeloid leukemia. The review includes references published over the last 10 y...
Despite the remarkable clinical response rates to imatinib in the treatment of bcr-abl leukemic pati...
Background: As imatinib pharmacokinetics are highly variable, plasma levels differ largely between p...
Besides affecting the systemic bioavailability of the parent drug, drug metabolizing enzymes (DMEs) ...
Imatinib has proved to be effective in the treatment of chronic myeloid leukemia, but plasma levels ...
Measurement of imatinib plasma concentration can be useful to evaluate patient adherence to daily or...
This retrospective multicenter study in patients with chronic myeloid leukemia in chronic phase was ...
OBJECTIVE: The goal of this study was to monitor imatinib mesylate therapeutically in the Tumor Biol...
The widely inter-individual pharmacokinetic variability of the tyrosine-kinase BCR-ABL1 inhibitor im...
This study assessed whether a cycle of "routine" therapeutic drug monitoring (TDM) for imatinib dosa...
Imatinib at 400 mg daily is standard treatment for chronic myeloid leukemia in chronic phase. We her...
Imatinib treatment for chronic myeloid leukemia (CML) could be optimized by Therapeutic Drug Monitor...
The anticancer drug imatinib has transformed the treatment and prognosis of chronic myeloid leukemia...
The LC-ESI-MS was developed and validated for the analysis of imatinib in plasma and bone marrow sam...
Introduction: As imatinib pharmacokinetics are highly variable, plasma levels differ largely between...
Current routine monitoring strategies for chronic myeloid leukemia (CML) incorporate hematologic, cy...
Despite the remarkable clinical response rates to imatinib in the treatment of bcr-abl leukemic pati...
Background: As imatinib pharmacokinetics are highly variable, plasma levels differ largely between p...
Besides affecting the systemic bioavailability of the parent drug, drug metabolizing enzymes (DMEs) ...
Imatinib has proved to be effective in the treatment of chronic myeloid leukemia, but plasma levels ...
Measurement of imatinib plasma concentration can be useful to evaluate patient adherence to daily or...
This retrospective multicenter study in patients with chronic myeloid leukemia in chronic phase was ...
OBJECTIVE: The goal of this study was to monitor imatinib mesylate therapeutically in the Tumor Biol...
The widely inter-individual pharmacokinetic variability of the tyrosine-kinase BCR-ABL1 inhibitor im...
This study assessed whether a cycle of "routine" therapeutic drug monitoring (TDM) for imatinib dosa...
Imatinib at 400 mg daily is standard treatment for chronic myeloid leukemia in chronic phase. We her...
Imatinib treatment for chronic myeloid leukemia (CML) could be optimized by Therapeutic Drug Monitor...
The anticancer drug imatinib has transformed the treatment and prognosis of chronic myeloid leukemia...
The LC-ESI-MS was developed and validated for the analysis of imatinib in plasma and bone marrow sam...
Introduction: As imatinib pharmacokinetics are highly variable, plasma levels differ largely between...
Current routine monitoring strategies for chronic myeloid leukemia (CML) incorporate hematologic, cy...
Despite the remarkable clinical response rates to imatinib in the treatment of bcr-abl leukemic pati...
Background: As imatinib pharmacokinetics are highly variable, plasma levels differ largely between p...
Besides affecting the systemic bioavailability of the parent drug, drug metabolizing enzymes (DMEs) ...