Leukemia
Conditions
Keywords
recurrent adult acute myeloid leukemia, adult acute basophilic leukemia, adult acute eosinophilic leukemia, adult acute megakaryoblastic leukemia (M7), adult acute myeloblastic leukemia with maturation (M2), adult acute myelomonocytic leukemia (M4), adult acute monoblastic leukemia (M5a), adult acute monocytic leukemia (M5b), adult acute myeloblastic leukemia without maturation (M1), adult erythroleukemia (M6a), adult pure erythroid leukemia (M6b), blastic phase chronic myelogenous leukemia, relapsing chronic myelogenous leukemia
Brief summary
RATIONALE: Drugs used in chemotherapy, such as cladribine and cytarabine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Imatinib mesylate may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving cladribine and cytarabine together with imatinib mesylate may kill more cancer cells. PURPOSE: This phase I trial is studying the side effects and best dose of imatinib mesylate when given together with cladribine and cytarabine in treating patients with refractory or relapsed acute myeloid leukemia or blastic phase chronic myelogenous leukemia.
Detailed description
OBJECTIVES: * Determine the safety and feasibility of cladribine, cytarabine, and imatinib mesylate in patients with refractory or relapsed acute myeloid leukemia or blastic phase chronic myelogenous leukemia. * Determine the maximum tolerated dose of imatinib mesylate in patients treated with this regimen. * Correlate the expression of c-kit and the presence of c-kit mutations with clinical response in patients treated with this regimen. * Correlate the in vitro inhibitory effects of imatinib mesylate and cytarabine on the proliferation and survival of leukemic cells with clinical response in patients treated with this regimen. OUTLINE: This is a dose-escalation study of imatinib mesylate. Patients receive oral imatinib mesylate once daily on days 1-15 and cladribine IV over 2 hours and cytarabine IV over 4 hours on days 3-7. Patients also receive filgrastim (G-CSF) subcutaneously on days 2-7. Treatment repeats every 15 days for 2 courses in the absence of disease progression or unacceptable toxicity. Cohorts of 3-6 patients receive escalating doses of imatinib mesylate until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. After completion of study treatment, patients are followed periodically for up to 1 year. PROJECTED ACCRUAL: A total of 12-18 patients will be accrued for this study.
Interventions
BIOLOGICALfilgrastim
DRUGcladribine
DRUGcytarabine
DRUGimatinib mesylate
Sponsors
University of Rochester
Study design
Primary purpose
TREATMENT
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * Diagnosis of acute myeloid leukemia (AML) or blastic phase chronic myelogenous leukemia (CML) * Refractory AML defined as any of the following: * Failure to achieve complete response (CR) after 2 courses of induction chemotherapy * Persistent bone marrow blasts \> 40% after 1 course of induction chemotherapy * Relapse of disease within 3 months since CR * Relapsed AML defined as the following: * Any evidence of disease recurrence after CR (early relapse occurs within 3-12 months and late relapse occurs \> 12 months later) * No acute promyelocytic leukemia (AML-M3 FAB subgroup) PATIENT CHARACTERISTICS: Performance status * ECOG 0-2 Life expectancy * Not specified Hematopoietic * Not specified Hepatic * Bilirubin ≤ 2.0 mg/dL * AST ≤ 2.5 times upper limit of normal * No known chronic liver disease (e.g., chronic active hepatitis or cirrhosis) Renal * Creatinine \< 2.5 mg/dL (if 2.0-2.5 mg/dL, glomerular filtration rate must be measured and dose of cytarabine adjusted if necessary) Cardiovascular * No New York Heart Association grade III-IV heart disease * No congestive heart failure * No myocardial infarction within the past 6 months * Ejection fraction ≥ 30% Other * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective barrier contraception during and for 3 months after completion of study treatment * No uncontrolled systemic active infection * No known HIV infection * No history of allergic reaction attributed to compounds of similar chemical or biological composition to study drugs * No history of other curatively treated malignancy except nonmelanoma skin cancer PRIOR CONCURRENT THERAPY: Biologic therapy * No other concurrent biologic agents Chemotherapy * See Disease Characteristics * No other concurrent chemotherapy Endocrine therapy * No concurrent birth control pills Other * More than 1 week since any prior investigational agent * No other concurrent investigational agents or therapies * No other concurrent anticancer agents * No concurrent therapeutic anticoagulation with warfarin * Low molecular weight heparin or heparin allowed for therapeutic anticoagulation * Mini-dose warfarin (e.g., 1 mg per day) allowed for prophylaxis of central venous catheter thrombosis
Countries
United States
Outcome results
None listed