Recurrent Adult Acute Myeloid Leukemia Clinical Trial
Official title:
A Phase II Trial of Clofarabine and Cytarabine to Treat Minimal Residual Disease (MRD) in Acute Myeloid Leukemia
RATIONALE: Drugs used in chemotherapy, such as clofarabine and cytarabine, work in different
ways to stop the growth of cancer cells, either by killing the cells or by stopping them
from dividing. Giving clofarabine together with cytarabine may kill more cancer cells.
PURPOSE: This pilot phase II trial is studying how well giving clofarabine together with
cytarabine works in treating patients with acute myeloid leukemia with minimal residual
disease
PRIMARY OBJECTIVES:
I. To test the ability of clofarabine + ara-C (cytarabine) to eliminate minimal residual
(MRD) in acute myeloid leukemia (AML) patients whose bone marrows exhibit complete remission
by morphology.
SECONDARY OBJECTIVES:
I. To determine the duration of complete remission after this treatment to minimize MRD.
OUTLINE:
Patients receive filgrastim (G-CSF) subcutaneously (SC) once daily (QD) on days 1-5 and
clofarabine intravenously (IV) over 1 hour and cytarabine IV on days 2-5. Beginning
approximately 1 month later, patients may receive one additional course of treatment in the
absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up every 3 months for 2 years,
and then annually for 3 years.
;
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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