Leukemia
Conditions
Keywords
recurrent childhood acute lymphoblastic leukemia, recurrent childhood acute myeloid leukemia, recurrent adult acute myeloid leukemia, recurrent adult acute lymphoblastic leukemia, adult acute lymphoblastic leukemia in remission, childhood acute lymphoblastic leukemia in remission, acute undifferentiated leukemia, secondary acute myeloid leukemia
Brief summary
RATIONALE: Transplanted peripheral stem cells can sometimes be rejected by the body's tissues. Treating donor peripheral stem cells with filgrastim may increase the number of donor white blood cells. This may help to decrease the rejection of the transplanted cells in patients receiving them as treatment for acute leukemia. PURPOSE: Phase II trial to study the effectiveness of filgrastim-treated donor peripheral stem cells in treating patients with acute leukemia who are undergoing peripheral stem cell transplantation.
Detailed description
OBJECTIVES: * Determine whether filgrastim (G-CSF)-mobilized allogeneic peripheral blood stem cell transplantation reduces the incidence of non-leukemic mortality in patients with acute leukemia. * Determine the kinetics and durability of engraftment after treatment with this regimen in these patients. * Determine the incidence and severity of acute and chronic graft-versus-host disease in patients treated with this regimen. * Determine the leukemia-free survival of patients treated with this regimen. OUTLINE: Donors receive filgrastim (G-CSF) subcutaneously (SC) on days -5 to -1. Donors then undergo leukapheresis on days -1 and 0. Patients undergo total body irradiation twice daily on days -7 to -4. Patients receive 2 doses of intrathecal methotrexate per local guidelines between days -10 and -3. Patients also receive cyclophosphamide IV on days -3 and -2. Patients receive infusion of allogeneic peripheral blood stem cells on day 0. PROJECTED ACCRUAL: A total of 5-60 patients will be accrued for this study within 3 years.
Interventions
DRUGcyclophosphamide
DRUGmethotrexate
PROCEDUREperipheral blood stem cell transplantation
RADIATIONradiation therapy
Sponsors
National Cancer Institute (NCI)
Fred Hutchinson Cancer Center
Study design
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
No minimum to 55 Years
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * One of the following diagnoses: * Primary acute leukemia beyond first remission * High-risk acute myelogenous leukemia * Acute lymphoblastic leukemia in first remission * Must have HLA-matched donor identical for HLA-A, -B, and DRB1 alleles * No HLA-matched identical sibling or haploidentical relative incompatible for 0 or 1 HLA-A, -B, or -DRB1 loci on the non-shared haplotype * No leukoencephalopathy PATIENT CHARACTERISTICS: Age: * 55 and under Performance status: * Not specified Life expectancy: * Not specified Hematopoietic: * Not specified Hepatic: * SGOT no greater than 2 times normal * Hepatitis B surface antigen negative * No prior hepatitis C Renal: * No impaired renal function * Creatinine less than 2 times normal Cardiovascular: * No symptomatic cardiac disease Pulmonary: * No active pulmonary disease * DLCO at least 60% predicted Other: * HIV negative * No disease or other malignancy that severely limits life expectancy * No severe or life-threatening infection within the past 2 weeks * No history of septate fungal infection or disseminated candidiasis PRIOR CONCURRENT THERAPY: Biologic therapy: * No prior bone marrow or peripheral blood stem cell transplantation Chemotherapy: * Not specified Endocrine therapy: * Not specified Radiotherapy: * No prior radiotherapy greater than 3,000 cGy to whole brain * No prior radiotherapy of 1,500 cGy to chest or abdomen * At least 6 months since prior involved-field radiotherapy to chest or abdomen Surgery: * Not specified
Countries
United States
Outcome results
None listed