Therapy of Early Chronic Phase CML With Gleevec
Leukemia, Myeloid, Chronic-Phase
About this trial
This is an interventional treatment trial for Leukemia, Myeloid, Chronic-Phase focused on measuring Early Chronic Phase Chronic Myelogenous Leukemia, Leukemia, Gleevec, STI571, Imatinib mesylate
Eligibility Criteria
Inclusion Criteria: Diagnosis of Philadelphia chromosome (Ph)- positive or breakpoint cluster region (bcr)-positive CML in early chronic (diagnosis < 12 months). Age 15 years or above Adequate renal, hepatic, cardiac and performance status (ECOG 0-2) - no psychiatric disability (psychosis) Signed informed consent Exclusion Criteria: Grade 3-4 cardiac Psychiatric problem Pregnant or lactating
Sites / Locations
- UT MD Anderson Cancer Center
Arms of the Study
Arm 1
Experimental
Gleevec
Gleevec 400 mg orally daily. Dose adjustments made at discretion of treating physician within these guidelines: The highest dose acceptable is 800 mg daily. The lowest dose acceptable is 300 mg. No dose adjustment of more than 200 mg at one time is allowed. Dose adjustments to less than 300 mg may be approved after consultation with the principal investigator.