Leukemia, Myeloid, Acute
Conditions
Brief summary
The main objective is to determine the safety and tolerability of combination decitabine and bexarotene during four cycles of therapy.
Detailed description
The investigators are seeking to study the combination of decitabine and bexarotene. These two agents have each shown efficacy in decreasing leukemic blast counts and restoring normal hematopoiesis via different mechanisms of action and with non-overlapping side-effect profiles. By combining these agents, the investigators hope to improve overall response rates. The investigators further hope to improve platelet and neutrophil counts in an even greater number of patients, thus treating two of the most important sources of morbidity and mortality in this patient population.
Interventions
DRUGDecitabine
DRUGBexarotene
Sponsors
Washington University School of Medicine
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* AML with bone marrow blasts ≥ 20%. * Relapsed disease after 1 or more lines of prior salvage chemotherapy and any FAB-AML, or * Diagnosis of AML and age ≥ 60 and not a candidate for cytotoxic chemotherapy and any FAB-AML except FAB-M3. * Performance status ≤ 2. * Age ≥ 18 years.
Exclusion criteria
* Peripheral white blood cell count (WBC) \> 10,000/microliter. * Total bilirubin \> 1.5 x normal. * AST/ALT \> 2.5 x normal. * Serum creatinine \> 2 x normal. * Fasting serum triglyceride \> 1,000 mg/dL. * Active or poorly controlled graft vs host disease (GVHD). * Pregnant or nursing. * Known CNS leukemia. * History of positive HIV serology. * History of positive Hepatitis C serology. * Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, congestive heart failure of NYHA class 3 or 4, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situation that would limit compliance with study requirements. * Chemotherapy within 21 days of enrollment. * Radiation therapy within 14 days of enrollment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Toxicity of combination decitabine and bexarotene during four cycles of therapy | After 4 cycles of therapy |
Secondary
| Measure | Time frame |
|---|---|
| To determine the rates of hematological improvement, transfusion independence, time to progression, cytogenetic response, and survival. | Every 2 months for 2 years after first dose of study drug |
| To perform correlative studies defining transcriptional response to bexarotene in primary AML bone marrow cells. | Baseline, C1D3, Day 25 of even cycles, and End of Study treatment |
| To determine the complete remission (CR) and partial remission (PR) rate after four cycles of therapy. | After 4 cycles of therapy |
| To perform correlative studies comparing the self-renewal of morphologically differentiated neutrophils and leukemic blasts by colony forming assays in patients with improved neutrophil counts. | Baseline, C1D3, Day 25 of even cycles, and End of Study treatment |
| To perform correlative studies of platelet function by PFA100 in patients with platelet counts improved to >100,000/microliter | Baseline, C1D3, Day 25 of even cycles, and End of Study treatment |
| To perform correlative studies examining the clonality of morphologically differentiated neutrophils by fluorescence in situ hybridization (FISH) in patients with improved neutrophil counts. | Baseline, C1D3, Day 25 of even cycles, and End of Study treatment |
Countries
United States
Outcome results
None listed