Adult Acute Promyelocytic Leukemia (M3), Blastic Phase Chronic Myelogenous Leukemia, Childhood Myelodysplastic Syndromes, Previously Treated Myelodysplastic Syndromes, Recurrent Adult Acute Lymphoblastic Leukemia, Recurrent Adult Acute Myeloid Leukemia, Recurrent Childhood Acute Lymphoblastic Leukemia, Recurrent Childhood Acute Myeloid Leukemia, Refractory Anemia With Excess Blasts, Refractory Anemia With Excess Blasts in Transformation, Relapsing Chronic Myelogenous Leukemia
Conditions
Brief summary
Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Phase I trial to study the effectiveness of BMS-214662 in treating patients who have acute leukemia, myelodysplastic syndrome, or chronic myeloid leukemia in blast phase
Detailed description
PRIMARY OBJECTIVES: I. Determine the maximum tolerated dose and dose limiting toxicity of BMS-214662 in patients with acute leukemia, myelodysplastic syndrome, or chronic myeloid leukemia in blast phase. II. Determine any preliminary evidence of antileukemia activity of this drug in these patients. OUTLINE: This is a dose escalation study. Patients receive BMS-214662 IV over 1 hour weekly for 4 weeks. Treatment continues every 4 weeks for a maximum of 12 courses in the absence of unacceptable toxicity or disease progression. Cohorts of 3-6 patients receive escalating doses of BMS-214662 until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 6 patients experience dose limiting toxicities. PROJECTED ACCRUAL: A maximum of 30 patients will be accrued for this study within 10 months.
Interventions
DRUGBMS-214662
Given IV
OTHERpharmacological study
Correlative studies
OTHERlaboratory biomarker analysis
Correlative studies
Sponsors
National Cancer Institute (NCI)
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients must have: * AML, ALL, or high-risk MDS (RAEB or RAEB-t) that has: * Not responded (no CR) to initial induction chemotherapy, or * Recurred after an initial CR of \< 1 year, or * Recurred after an initial CR of \> 1 year and failed to respond to an initial reinduction attempt, or * Recurred more than once, or * Chronic myeloid leukemia in myeloid blast phase * Patients with CML blast phase may receive BMS-214662 as their first therapy for blast phase or after failing other treatments for blast phase * Patients with refractory or relapsed acute promyelocytic leukemia are eligible provided they have failed an ATRA-containing regimen * Performance status of =\< 0-2 * Signed informed consent indicating that patients are aware of the investigational nature of this study in keeping with the policies of the hospital * Patients must have been off chemotherapy for the 4 weeks prior to entering this study and recovered from the toxic effects of that therapy; patients with evidence of rapidly progressive disease (i.e., absolute peripheral blood blast count \>= 5 x 10\^9/L and increasing by \>= 1 x 10\^9/L/24 hours) may receive treatment before 4 weeks from the previous treatment providing they have recovered from all toxic effects of that therapy; use of hydroxyurea on patients with rapidly proliferative disease is allowed up to 24 hours prior to the start of therapy * Bilirubin =\< 1.5 mg/dL * Creatinine =\< 1.5 mg/dL or creatinine clearance \>= 60 mL/hr * Patients who are likely to benefit from allogeneic bone marrow transplantation (i.e., age \< 60 years of physiological age with histocompatible donor) should be excluded from this study unless such therapy is not feasible
Exclusion criteria
* Pregnant and nursing females will be excluded; patients of childbearing potential should practice effective methods of contraception * Patients with prolonged QTc interval on EKG are excluded
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| MTD defined as the dose preceding that at which 2 of 6 patients experience DLT assessed using NCI CTC version 2.0 | 4 weeks | Non-parametric tests will be used to study the relationship between baseline and post-therapy values at different dose levels and times. |
Countries
United States
Outcome results
None listed