Allogeneic Bone Marrow Transplantation for the Treatment of Genetic Disorders of Erythropoiesis

Clinical Trial
Study Details
Enrollment
25
Interventions
Description

Busulfan 0.8 or 1 mg/Kg/day Days 8-6 Cyclophosphamide 50 mg/Kg/day Days 2-5 BMT Day 0

Name
Busulfan, Cyclophosphamide, BMD
Type
Procedure
Phase
Phase 2
Status
COMPLETED
Study ID #
NCT00578435
Study Type
Interventional
Summary

The purpose of this study is to determine and confirm the role of bone marrow transplantation in the treatment of disorders of the red cell and hemoglobin including sickle cell anemia, thalassemia and diamond blackfan anemia.

Study Overview
Description

The trial proposed is a single armed phase II treatment protocol designed to examine the engraftment,toxicity and graft-versus-host disease following a novel cytoreductive regimen including cyclophosphamide and Busulfan for the treatment of patients with Severe Sickle Cell Anemia,Thalassemia, and Diamond Blackfan Anemia using stem cell transplants derived from HLA-genotypically identical siblings.

Patients will be conditioned for transplantation with cyclophosphamide (50 mg/kg/day x 4 days), and busulfan \[(if \< 4 years of age 1 mg/kg 4 times per day x 4 days), (if \> 4 years of age 0.8 mg/kg 4 times per day x 4 days)\]. Patients will receive Methotrexate \& Cyclosporin-A for prophylaxis against GvHD and GCSF to promote engraftment.

The preferred source of stem cells from related HLA-matched related donors will be unmodified bone marrow stem cells.

Contacts and Locations
Locations
Facility

Memorial Sloan-Kettering Cancer Center
New York, New York 10065
United States

GeoPoint
40.71427, -74.00597