This is a Phase II pilot study to evaluate engraftment and toxicity of patients with non-malignant diseases using a reduced intensity conditioning regimen in the setting of allogeneic transplant for non malignant diseases. Bone Marrow or cord blood will be acceptable as a stem cell source. Recently, reduced intensity conditioning (RIC) regimens have been used for both adult patients with leukemias and pediatric patients with non-malignant diseases. These regimens are better tolerated, resulting in less transplant related morbidity and mortality. Stable mixed chimerism, while insufficient for eradication of leukemias, may be sufficient to cure patients with non-malignant diseases.
There are two conditioning regimens in this protocol for children \>6 months. Alemtuzumab (Campath), Fludarabine and Melphalan are used. The regimens differ by the timing and dosing of Alemtuzumab (Campath). The two timings are distal and intermediate. * Distal campath is initiated 22 days prior to the allogeneic transplant. * Intermediate campath is initiated 14 days prior to allogeneic transplant. The conditioning regimen for children with immunodeficiencies \<6 months omits melphalan, and substitutes two days of busulfan. This regimen is successfully used in the United Kingdom, and has been successful in a 3 month old infant at the Children's Hospital of Philadelphia (CHOP) who engrafted with a haploidentical donor.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
75
Campath, Fludarabine, Melphalan, Cyclosporine, Cellcept (MMF)
Campath, Fludarabine, Melphalan, Cyclosporine, Cellcept (MMF)
Campath, Fludarabine, Busulfan, Cyclosporine, Cellcept (MMF)
The Children's Hospital of Philadelphia
Philadelphia, Pennsylvania, United States
Engraftment
engraftment of patients with non-malignant disorders will be evaluated using a reduced-intensity conditioning regimen
Time frame: Post Transplant -100 days
Survival
Event free survival will be evaluated by the time interval to either the primary or late graft failure, disease recurrence or death.
Time frame: 1 year post transplant
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