Combination Chemotherapy and Tipifarnib in Treating Patients With Newly Diagnosed Acute Myeloid Leukemia

Combination Chemotherapy and Tipifarnib in Treating Patients With Newly Diagnosed Acute Myeloid Leukemia

A Phase I Study of R115777 (Zarnestra) in Combination With Induction Chemotherapy in Patients With Newly Diagnosed, High Risk Acute Myeloid Leukemia

RATIONALE: Drugs used in chemotherapy, such as cytarabine, daunorubicin, and etoposide, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Tipifarnib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving combination chemotherapy together with tipifarnib may kill more cancer cells. PURPOSE: This phase I trial is studying the side effects and best dose of tipifarnib when given together with combination chemotherapy in treating patients with newly diagnosed acute myeloid leukemia.

OBJECTIVES: Primary Determine the maximum tolerated dose of tipifarnib when given in combination with induction therapy comprising cytarabine, daunorubicin, and etoposide followed by consolidation therapy comprising high-dose cytarabine in patients with newly diagnosed high-risk acute myeloid leukemia. Secondary Determine the qualitative and quantitative toxic effects of this regimen, in terms of organ specificity, time course, predictability, and reversibility, in these patients. Determine the rate of complete remission in patients treated with this regimen. Determine the remission duration, overall survival, and relapse-free and event-free survival of patients treated with this regimen. Determine the pharmacokinetics of this regimen in these patients. Correlate pharmacodynamic measurements and levels of tumor necrosis factor-alpha with clinical response in patients treated with this regimen. OUTLINE: This is a dose-escalation study of tipifarnib. Induction therapy: Patients receive cytarabine IV continuously on days 1-7; daunorubicin IV and etoposide IV over 2 hours on days 5-7; and oral tipifarnib twice daily on days 5-12. Patients undergo bone marrow biopsy on day 17 OR days 17 and 24 (if day 17 bone marrow biopsy shows suspicious disease). Patients achieving a complete remission (CR) proceed to consolidation therapy. Patients with residual disease, defined as > 5% leukemic blasts in a bone marrow of ≥ 20% cellularity, receive a second course of induction therapy comprising cytarabine IV continuously on days 1-5; daunorubicin IV and etoposide IV over 2 hours on days 4 and 5; and oral tipifarnib twice daily on days 4-9. Patients achieving a CR after a second course of induction therapy proceed to consolidation therapy. Patients not achieving a CR after a second course of induction therapy are removed from the study. Cohorts of 3-6 patients receive escalating doses of tipifarnib 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. An additional 12 patients are treated at the MTD. Consolidation therapy: Patients receive high-dose cytarabine IV twice daily on days 1, 3, and 5. Treatment repeats approximately every 6-8 weeks for 4 courses. After completion of study treatment, patients are followed every 3-6 months for up to 5 years. PROJECTED ACCRUAL: A maximum of 30 patients will be accrued for this study within 10-15 months.

adult acute myeloid leukemia with 11q23 (MLL) abnormalities, adult acute myeloid leukemia with t(16;16)(p13;q22), untreated adult acute myeloid leukemia, secondary acute myeloid leukemia

DISEASE CHARACTERISTICS: Histologically or cytologically confirmed acute myeloid leukemia (AML) according to the WHO classification system High-risk disease Newly diagnosed disease Patients with secondary AML due to prior chemotherapy for a different malignancy are eligible No known inv(16), t(8;21), or t(15;17) cytogenetic abnormality No acute promyelocytic leukemia No CNS leukemia PATIENT CHARACTERISTICS: Age 18 to 59 Performance status ECOG 0-2 Life expectancy More than 6 months Hematopoietic Not specified Hepatic AST and ALT ≤ 2.5 times upper limit of normal Bilirubin normal Renal Creatinine normal OR Creatinine clearance ≥ 60 mL/min Cardiovascular Ejection fraction > 50% by echocardiogram or MUGA No symptomatic congestive heart failure No unstable angina pectoris No cardiac arrhythmia Immunologic No known HIV positivity No history of allergic reactions attributed to compounds of similar chemical or biological composition to tipifarnib No allergy to imidazoles (e.g., clotrimazole, ketoconazole, miconazole, or econazole) No ongoing or active infection Other Not pregnant or nursing Negative pregnancy test Fertile patients must use effective contraception No other uncontrolled illness No psychiatric illness or social situation that would preclude study compliance PRIOR CONCURRENT THERAPY: Biologic therapy No concurrent epoetin alfa Chemotherapy See Disease Characteristics No prior chemotherapy for AML or myelodysplastic syndromes except hydroxyurea Endocrine therapy Not specified Radiotherapy No concurrent palliative radiotherapy Surgery Not specified Other More than 30 days since prior investigational agents No other concurrent investigational or commercial agents or therapies for the malignancy

Arthur G. James Cancer Hospital and Solove Research Institute at Ohio State University Medical Center