Bexarotene and GM-CSF in Treating Patients With Myelodysplastic Syndrome or Acute Myeloid Leukemia

OBJECTIVES:

Primary

- Assess the clinical response in patients with myelodysplastic syndromes or acute myeloid
leukemia treated with bexarotene and sargramostim (GM-CSF).

Secondary

- Determine the clinical activity of this regimen, in terms of transfusion requirements,
in these patients.

- Determine the biological activity of this regimen, in terms of biological markers and
cytogenetic abnormalities, in these patients.

- Assess the toxicity profile of this regimen in these patients.

OUTLINE: Patients receive oral bexarotene and sargramostim (GM-CSF) subcutaneously on days
1-28. Treatment repeats every 28 days for up to 6 courses in the absence of disease
progression or unacceptable toxicity.

Blood and bone marrow samples are collected at baseline and after 1 or 2 courses of study
therapy. Samples are examined by flow cytometry for laboratory studies, including biological
markers, and by fluorescent in situ hybridization (FISH) for cytogenetic changes.

After completion of study treatment, patients are followed periodically for 6 months.

PROJECTED ACCRUAL: A total of 18 patients will be accrued for this study.

DISEASE CHARACTERISTICS:

- Diagnosis (confirmed by bone marrow aspirate and/or biopsy) of 1 of the following:

- Myelodysplastic syndromes of 1 of the following cell types:

- Refractory anemia (RA) with ringed sideroblasts

- Refractory cytopenia with multilineage dysplasia (RCMD)

- RCMD and ringed sideroblasts

- RA with excess blasts-1

- RA with excess blasts-2

- Myelodysplastic syndromes, unclassified

- Chronic myelomonocytic leukemia

- Relapsed or refractory acute myeloid leukemia (AML), meeting 1 of the following
criteria:

- Recurrent genetic abnormalities (11q23 [MLL] abnormalities)

- Multilineage dysplasia

- Therapy-related AML

- Not otherwise categorized, including any of the following:

- M0 minimally differentiated

- M1 without maturation

- M2 with maturation

- M4 myelomonocytic leukemia

- M5 monoblastic/monocytic leukemia

- M6 erythroid leukemia

- M7 megakaryoblastic leukemia

- Newly diagnosed untreated AML allowed provided patient does not qualify for or refused
potentially curative intensive chemotherapeutic regimens

- No RA with 5q-syndrome

- No peripheral leukemia with blast count > 30,000/mm³ (uncontrolled with hydroxyurea)

- Relatively stable bone marrow function for > 7 days (i.e., no WBC doubling to >
10,000/mm^3)

- No acute promyelocytic leukemia

- No clinical symptoms of active CNS disease (if CNS disease is suspected, patient must
have lumbar puncture with negative cytology)

PATIENT CHARACTERISTICS:

- ECOG performance status 0-2

- Creatinine ≤ 2.0 mg/dL

- Bilirubin ≤ 1.6 mg/dL (unless secondary to hemolysis)

- AST and ALT ≤ 4 times upper limit of normal (unless disease related)

- Hemoglobin ≥ 8 g/dL (transfusions allowed)

- Not pregnant or nursing

- Negative pregnancy test

- Fertile patients must use effective barrier contraception

- No untreated positive blood cultures or progressive infection as assessed by
radiographic studies

- No history of intolerance to sargramostim (GM-CSF)

PRIOR CONCURRENT THERAPY:

- Recovered from prior therapy

- At least 2 weeks since prior treatment for myeloid disorder, including any of the
following:

- Chemotherapy

- Hematopoietic growth factors

- Biologic therapy (e.g., monoclonal antibodies)

- Hydroxyurea for patients with WBC > 10,000/mm^3 allowed

- No concurrent vitamin A supplementation

- No concurrent gemfibrozil