RATIONALE: Drugs used in chemotherapy, such as idarubicin and cytarabine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Pravastatin may help idarubicin and cytarabine work better by making cancer cells more sensitive to the drugs. Giving pravastatin together with idarubicin and cytarabine may kill more cancer cells.

PURPOSE: This phase I trial is studying the side effects and best dose of pravastatin when given together with idarubicin and cytarabine in treating patients with acute myeloid leukemia.

Condition	Treatment or Intervention	Phase
adult acute myeloid leukemia	Drug: cytarabine  Drug: idarubicin  Drug: pravastatin  Procedure: chemosensitization/potentiation  Procedure: chemotherapy  Procedure: high-dose chemotherapy	Phase I

Further Study Details: 

OBJECTIVES:

• Determine the biological efficacy of pravastatin in leukemia cells, in terms of measuring surrogate endpoints, including cellular cholesterol, messenger RNA encoding cholesterol synthesis, cholesterol import regulators, and specific protein farnesylation, in patients with acute myeloid leukemia.
• Determine whether increasing doses of pravastatin, when administered with idarubicin and high-dose cytarabine, produce increased apoptosis in leukemia cells of these patients.
• Determine the maximum tolerated dose (MTD) of pravastatin when administered with idarubicin and high-dose cytarabine in these patients.
• Determine whether the MTD of pravastatin is required to achieve the maximal biological effect on cholesterol metabolism in leukemia cells of these patients.

OUTLINE: This is an open-label, multicenter, dose-escalation study of pravastatin.

Patients receive oral pravastatin once daily on days 1-8, idarubicin IV over 30 minutes on days 4-6, and high-dose cytarabine IV continuously on days 4-7. Treatment repeats every 28-42 days for up to 6 courses in the absence of disease progression or unacceptable toxicity. Patients achieving a complete remission (CR) may receive additional treatment with the same doses of study drugs over fewer days. These patients receive oral pravastatin once daily on days 1-6 and idarubicin IV over 30 minutes and high-dose cytarabine IV continuously on days 4 and 5. Patients experiencing disease response with severe side effects may receive additional treatment at a lower dose of the study drug causing the side effects.

Cohorts of 3 patients receive escalating doses of pravastatin until the maximum tolerated dose (MTD)* is determined or a predetermined maximum dose is reached.

NOTE: *Patients achieving a CR with a dose of pravastatin that is subsequently determined to be above the MTD receive pravastatin at the MTD for all subsequent courses.

After completion of study treatment, patients are followed at least every 3 months for 2 years.

PROJECTED ACCRUAL: A total of 36 patients will be accrued for this study within 2 years.

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

DISEASE CHARACTERISTICS:

• Diagnosis of acute myeloid leukemia (AML) meeting 1 of the following criteria:
• Newly diagnosed disease
• In first or second relapse AND scheduled to receive first salvage therapy
• Primary refractory disease after prior induction therapy for newly diagnosed disease

PATIENT CHARACTERISTICS: Age

• Over 18

Performance status

• Zubrod 0-2

Life expectancy

• Not specified

Hematopoietic

• Not specified

Hepatic

• AST or ALT ≤ 2 times normal
• Alkaline phosphatase ≤ 2 times normal
• Bilirubin < 2.0 mg/dL
• No acute or chronic hepatic impairment

Renal

• Creatinine < 1.5 times normal (unless secondary to acute myeloid leukemia)

Cardiovascular

• Ejection fraction (EF) ≥ 45% by MUGA or 2-D echocardiogram
• Patients who have an EF < 45% OR cardiac symptoms must be evaluated and cleared by cardiology to be eligible for study entry
• No cardiac contraindication to idarubicin

Other

• Not pregnant or nursing
• Fertile patients must use effective contraception
• HIV negative
• No uncontrolled or life threatening infection
• No known intolerance to study drugs
• Must be able to safely tolerate the 3-day delay between the start of pravastatin and the start of chemotherapy

PRIOR CONCURRENT THERAPY: Biologic therapy

• Not specified

Chemotherapy

• Not specified

Endocrine therapy

• Not specified

Radiotherapy

• Not specified

Surgery

• Not specified

Other

• No other concurrent HMG-CoAR inhibitors, including any of the following:
• Atorvastatin
• Fluvastatin
• Lovastatin
• Rosuvastatin
• Simvastatin
• No concurrent non-HMG-CoAR inhibitors to lower cholesterol
• No concurrent use of any of the following medications:
• Bezafibrate
• Clofibrate
• Fenofibrate
• Gemfibrozil
• Cholestipol
• Cholestyramine resin
• Colesevelam
• Ezetimibe
• Biphenabid
• Niacin

Texas
      MD Anderson Cancer Center at University of Texas, Houston,  Texas,  77030-4009,  United States; Recruiting
Washington
      Fred Hutchinson Cancer Research Center, Seattle,  Washington,  98109-1024,  United States; Recruiting

Study chairs or principal investigators

Stephen H. Petersdorf, MD,  Principal Investigator,  Fred Hutchinson Cancer Research Center   

Study ID Numbers:  CDR0000419678; FHCRC-1945.00; MDA-2004-0185
Record last reviewed:  March 2005
Last Updated:  April 5, 2005
Record first received:  April 5, 2005
ClinicalTrials.gov Identifier:  NCT00107523
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08