Study of Stem Cell Transplant for Leukemia and Myelodysplastic Syndromes Using Clofarabine and Busulfan Regimen

Baylor Scott and White Health (BSWH)

Status and phase

Completed

Phase 2

Conditions

Myelodysplastic Syndrome

Leukemia

Treatments

Drug: Clofarabine with Busulfan

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00852163

006-150

Details and patient eligibility

About

The purpose of this study is to determine whether Clofarabine in combination with Busulfan is effective as a preparative transplant regimen for the treatment of leukemia and myelodysplastic syndromes

Full description

The success of allogeneic hematopoietic transplantation in the treatment of myeloid malignancies is determined by two main factors: the limiting of regimen-related toxicity and the prevention of recurrent leukemia. Over the past 10 years, considerable clinical research has been devoted to the reduction of regimen-related toxicity through the use of reduced-intensity (nonmyeloablative) transplants. However, leukemic relapse has remained a difficult obstacle. Thus, the need for highly effective, yet non-toxic regimens persists, particularly for elderly patients for whom very little overall progress has been made. Clofarabine is a chemotherapeutic agent with novel myelotoxic properties and proven low toxicity in older patients. These qualities suggest clofarabine may be a useful component of conditioning regimens for stem cell transplantation.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Disease Criteria:

Acute myelogenous leukemia (AML)
Acute lymphocytic leukemia (ALL)
Myelodysplastic syndromes (MDS) Refractory anemia (RA) with adverse cytogenetics (SWOG criteria) or beyond (RAEB, RAEB-T, AML)
Other Myeloproliferative Disorders Myelofibrosis, Agnogenic Myeloid Metaplasia, Chronic Myelomonocytic Leukemia (CMML)
Chronic lymphocytic leukemia (CLL) High risk or advanced disease

Other Inclusion Criteria:

18 years of age or older
Related or unrelated donor with HLA criteria as follows:
- Related donors: a serologic equivalent HLA Class I (A, B, and C) and Class II DRB1 or DQB1 matched donor OR a donor who is a single 1 antigen mismatched for A, B, C, DRB1, or DQB1 loci
- Unrelated donors: sequence-based typing fully matched A, B, C, DRB1, and DQB1 allele-matched donor OR a donor who is no greater than 1 antigen mismatched for A, B, C, DRB1, or DQB1 loci
Able to provide valid informed consent.
Female patients must have a negative serum pregnancy test within 2 weeks prior to enrollment.
Male and female patients must use an effective contraceptive method during the study and for up to 12 months after study treatment.

Exclusion criteria

Organ Function Criteria:

Cardiac: symptomatic coronary artery disease or ejection fraction <45% or uncontrolled cardiac failure
Pulmonary: FEV1 or DLCO (corrected) <50% of predicted values and/or receiving continuous supplementary oxygen
Hepatic: Bilirubin ≥ 1.2 mg/dL or AST/ALT ≥ 3x upper limit of normal (ULN) unless the liver is involved with malignant disease
Renal: creatinine clearance < 60 mL/min (24-hour urine collection) or <50 mL/min (Glofil test)
Karnofsky score <60%
Active CNS disease
Prior hematopoietic transplantation (autologous or allogeneic) <6 months prior to study entry
Use of investigational agents less than or equal to 30 days before study entry.
Life threatening, or clinically significant infection
Any significant concurrent disease, illness, or psychiatric disorder that would compromise patient safety or compliance, interfere with consent, study participation, follow up, or interpretation of study results.
Female patients who are pregnant or breast feeding
HIV-positive