FR901228 in Treating Patients With Myelodysplastic Syndrome, Acute Myeloid Leukemia, or Non-Hodgkin's Lymphoma

Memorial Sloan Kettering Cancer Center (MSK)

Status and phase: Completed; Phase 2

Conditions: Lymphoma; Leukemia; Myelodysplastic Syndromes; Myelodysplastic/Myeloproliferative Neoplasms

Treatments: Drug: romidepsin

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00042822

CDR0000069473

MSKCC-00116

NCI-1715

Details and patient eligibility

About

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 FR901228 in treating patients who have myelodysplastic syndrome, acute myeloid leukemia, or non-Hodgkin's lymphoma.

Full description

OBJECTIVES:

• Determine the pattern of adverse clinical experience in patients with myelodysplastic syndrome, acute myeloid leukemia, or intermediate-grade or follicular non-Hodgkin's lymphoma treated with FR901228 (depsipeptide).
• Determine the disease response in patients treated with this drug.
• Determine the pharmacokinetic and pharmacodynamic correlates of this drug, including measurement of serum plasma levels, H3 and H4 acetylation, apoptosis induction, differentiation, and multidrug-resistant (MDR) phenotype expression in these patients.

OUTLINE: Patients receive FR901228 (depsipeptide) IV over 4 hours on days 1 and 5. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Patients are followed monthly.

PROJECTED ACCRUAL: A total of 12 patients will be accrued for this study within 1 year.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• One of the following diagnoses:

  • Histologically confirmed refractory or relapsed acute myeloid leukemia (AML)

    • Failed anthracycline-based chemotherapy
    • Ineligible for or refused allogeneic stem cell transplantation

  • Elderly patients with newly diagnosed AML

    • Ineligible for or refused standard chemotherapy

  • Histologically confirmed high-risk myelodysplastic syndromes

    • Eligible subtypes include:

      • Refractory anemia with excess blasts (RAEB)
      • RAEB in transformation
      • Chronic myelomonocytic leukemia

    • Ineligible for or refused allogeneic bone marrow transplantation

  • Histologically confirmed intermediate-grade non-Hodgkin's lymphoma (NHL)

    • Relapsed after high-dose therapy OR
    • Ineligible for allogeneic or autologous stem cell transplantation
    • Evaluable lesions by radiologic study or physical examination

  • Histologically confirmed follicular NHL

    • Progressed after anthracycline-based chemotherapy and rituximab
    • Evaluable lesions by radiologic study or physical examination NOTE: A new classification scheme for adult non-Hodgkin's lymphoma has been adopted by PDQ. The terminology of "indolent" or "aggressive" lymphoma will replace the former terminology of "low", "intermediate", or "high" grade lymphoma. However, this protocol uses the former terminology.

PATIENT CHARACTERISTICS:

Age

• 18 and over

Performance status

• Karnofsky 60-100%

Life expectancy

• Not specified

Hematopoietic

• Not specified

Hepatic

• Bilirubin no greater than 1.5 mg/dL (unless due to Gilbert's syndrome)
• SGOT and SGPT less than 2 times upper limit of normal

Renal

• Creatinine no greater than 1.5 mg/dL OR
• Creatinine clearance at least 60 mL/min

Cardiovascular

• Cardiac ejection fraction greater than 50%
• No cardiac hypertrophy
• No known conduction heart disease
• No New York Heart Association class III or IV heart disease that would make it difficult to assess patient during study participation
• No significant prior heart disease
• No significant prior secondary or tertiary heart block
• No significant prior atrial or ventricular arrhythmia requiring therapeutic intervention or antiarrhythmics for rate control

Pulmonary

• No severe debilitating pulmonary disease that would make it difficult to assess patient during study participation

Other

• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception during and for 1 month after study participation
• Potassium ≥ 4.0 mmol/L (supplementation allowed)
• Magnesium ≥ 2.0 mg/dL (supplementation allowed)
• No other concurrent active malignancy except basal cell skin cancer
• No other concurrent significant co-morbidity that would make it difficult to assess patient during study participation

PRIOR CONCURRENT THERAPY:

Biologic therapy

• See Disease Characteristics
• At least 2 weeks since prior epoetin alfa or filgrastim (G-CSF)
• At least 4 weeks since prior cytokines
• No concurrent immunotherapy

Chemotherapy

• See Disease Characteristics
• At least 4 weeks since prior systemic chemotherapy
• No other concurrent chemotherapy

Endocrine therapy

• Not specified

Radiotherapy

• At least 4 weeks since prior radiotherapy
• No concurrent radiotherapy

Surgery

• Not specified

Other

• No other concurrent investigational agents

• No concurrent drugs that may prolong the QTc interval

  • FR901228 (depsipeptide) may be administered after a 5-half-life washout period following the use of these drugs