Leukemia Clinical Trial
Official title:
Fludarabine, Campath, TBI T-Cell Deplete NMSCT With Post-Transplant T-Cell Infusions for CML Failing Imatinib Therapy With Imatinib (STI571)
RATIONALE: Giving low doses of chemotherapy, such as fludarabine, and total-body irradiation
(TBI) before a donor stem cell transplant helps stop the growth of cancer cells. It also
stops the patient's immune system from rejecting the donor's stem cells. The donated stem
cells may replace the patient's immune system and help destroy any remaining cancer cells
(graft-versus-tumor effect). Giving an infusion of the donor's T cells (donor lymphocyte
infusion) that have been treated in the laboratory after the transplant may help increase
this effect. Sometimes the transplanted cells from a donor can also make an immune response
against the body's normal cells. Giving cyclosporine and alemtuzumab, and removing the T
lymphocyte cells(T cells) from the donor cells before transplant, may stop this from
happening.
PURPOSE: This clinical trial is studying how well giving fludarabine, alemtuzumab, and
total-body irradiation together with donor stem cell transplant and donor white blood cell
(WBC) infusion works in treating patients with chronic phase chronic myelogenous leukemia
(CML) that did not respond to previous imatinib mesylate.
OBJECTIVES:
- Determine the treatment-related mortality in patients with imatinib mesylate-resistant
chronic phase chronic myelogenous leukemia treated with nonmyeloablative conditioning
comprising fludarabine, alemtuzumab, and total-body irradiation followed by
T-cell-depleted allogeneic stem cell transplantation and post-transplantation allogeneic
T-cell infusion.
- Determine if donor engraftment can be safely established using partial T-cell depletion
with additional T-cell infusions in these patients.
OUTLINE: Patients receive alemtuzumab IV over 5-6 hours on day -8 and fludarabine IV on days
-4 to -2. Patients undergo total-body irradiation followed by T-cell-depleted (CD34+
selected) allogeneic stem cell transplantation on day 0. Patients receive allogeneic T-cell
infusion on days 30 and 60. Patients also receive cyclosporine twice daily beginning on day
-3 and continuing until day 100 followed by a taper until day 177.
PROJECTED ACCRUAL: Not specified.
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