RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. PURPOSE: Phase II trial to study the effectiveness of 506U78 in treating patients who have recurrent or refractory acute lymphocytic leukemia.
OBJECTIVES: * Assess the complete remission rate in patients with recurrent or refractory non-T-cell acute lymphocytic leukemia when treated with 506U78. * Determine the frequency and severity of toxic effects of this drug in these patients. OUTLINE: This is a multicenter study. Patients receive 506U78 IV over 2 hours on days 1, 3, and 5. Treatment continues every 21 days for up to 4 courses in the absence of disease progression or unacceptable toxicity. Patients are followed every month for 6 months, every 3 months for 1 year, and then every 6 months for 3.5 years. PROJECTED ACCRUAL: A total of 20-35 patients will be accrued for this study within 18 months.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
35
1.5 gm/m2 IV over 2 hours days 1, 3, 5 q21 days
CR
Time frame: After induction therapy is completed
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