Fludarabine Phosphate, Radiation Therapy, and Rituximab in Treating Patients Who Are Undergoing Donor Stem Cell Transplant Followed by Rituximab for High-Risk Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma
Part of paid clinical trials in Rochester, Minnesota.
- Sponsor
- Fred Hutchinson Cancer Center
- Study ID
- NCT00104858
- Phase
- PHASE2
- Status
- Completed
Conditions
- Chronic Lymphocytic Leukemia
- Prolymphocytic Leukemia
- Recurrent Small Lymphocytic Lymphoma
- Refractory Chronic Lymphocytic Leukemia
- Stage III Chronic Lymphocytic Leukemia
- Stage III Small Lymphocytic Lymphoma
- Stage IV Chronic Lymphocytic Leukemia
- Stage IV Small Lymphocytic Lymphoma
- T-Cell Large Granular Lymphocyte Leukemia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Allogeneic Hematopoietic Stem Cell Transplantation — PROCEDUREUndergo HSCT
- Cyclosporine — DRUGGiven PO
- Fludarabine Phosphate — DRUGGiven IV
- Laboratory Biomarker Analysis — OTHERCorrelative studies
- Mycophenolate Mofetil — DRUGGiven PO
- Peripheral Blood Stem Cell Transplantation — PROCEDUREUndergo HSCT
- Pharmacological Study — OTHERCorrelative studies
- Rituximab — BIOLOGICALGiven IV
- Total-Body Irradiation — RADIATIONUndergo TBI
Study Details
This phase II trial studies how well fludarabine phosphate with radiation therapy and rituximab followed by donor stem cell infusions work in treating patients with high-risk chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) with low side effects. Nonmyeloablative stem cell transplants use low doses of chemotherapy (fludarabine phosphate) and radiation to suppress the patient's immune system enough to prevent rejection of the donor's stem cells. Following infusion of donor stem cells, a mixture of the patient's and the donor's stem cells will exist and is called "mixed chimerism". Donor cells will attack the patient's leukemia. This is called the "graft-versus-leukemia" effect. Rituximab will be given 3 days before and three times after infusing stem cells to help in controlling CLL early after transplant till the "graft-versus-leukemia" takes control. Further, rituximab could augment the "graft-versus-leukemia" effect by activating donor immune cells and hence improve disease control. Sometimes the transplanted cells from a donor can also attack the body's normal cells. Giving cyclosporine and mycophenolate mofetil after the transplant may stop this from happening.
Key Dates
- Start date
- Dec 31, 2004
- Status verified
- Jun 2019
- Primary completion
- Mar 30, 2018
- Completion
- Mar 30, 2018
Study Design
- Enrollment
- 66 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: TreatmentPatients receive a conditioning regimen comprising fludarabine IV on days -4 to -2 and rituximab IV on days -3, 10, 24, and 38. Patients undergo single fraction low-dose TBI on day 0. After completion of TBI, patients undergo allogeneic hematopoietic stem cell transplantation on day 0. Patients then receive rituximab IV on days 10, 24, and 38. Patients receive an immunosuppressive regimen comprising cyclosporine PO BID on days -3 to 56 followed by a taper to day 180 (related recipients) or on days -3 to 100 followed by a taper to day 180 (unrelated recipients). Patients also receive mycophenolate mofetil PO BID on days 0-27 (related recipients) or TID on days 0-40 followed by a taper to day 96 (unrelated recipients).
Primary Outcome Measure
Overall Survival [ Time Frame: At 18 months ]
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Mayo Clinic | Rochester | Minnesota | 55905 | - |
| Fred Hutch/University of Washington Cancer Consortium | Seattle | Washington | 98109 | - |
| VA Puget Sound Health Care System | Seattle | Washington | 98101 | - |
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