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Clinical Trials/NCT00578435
NCT00578435
Completed
Phase 2

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

Memorial Sloan Kettering Cancer Center1 site in 1 country25 target enrollmentJanuary 1994

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Genetic Disorders
Sponsor
Memorial Sloan Kettering Cancer Center
Enrollment
25
Locations
1
Primary Endpoint
Define the role of bone marrow transplantation for the treatment of sickle cell disease and the reversibility of sickle cell vasculopathy and organ damage, good risk thalassemia major and Diamond-Blackfan Anemia.
Status
Completed
Last Updated
17 years ago

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
January 1994
End Date
August 2008
Last Updated
17 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Patients with severe HOMOZYGOUS SICKLE CELL ANEMIA or SICKLE/BETA THALASSEMIA
  • Neurologic event (stroke or hemorrhage).
  • Abnormal cerebral MRI scan and cerebral arteriogram or MRI angiographic study (MRA) and impaired neuropsychologic testing.
  • Recurrent acute chest syndrome (\> 2 episodes)
  • Stage I-II sickle chronic lung disease
  • Sickle cell nephropathy (moderate or severe proteinuria or GFR 30-50% of predicted for age.
  • Major visual impairment in at least one eye with bilateral proliferative retinopathy.
  • Osteonecrosis of multiple bones
  • Chronic debilitating pain secondary to vasoocclusive crisis (\>= 3 episodes per year for \>= 3 years) Recurrent priapism
  • Allo-immunization with the development of antibodies following chronic transfusion therapy

Exclusion Criteria

  • Patients whose life expectancy is less than 8 weeks. Patients with a Karnofsky or Lansky performance score of \< 70%
  • Patients with severe major organ dysfunction:
  • Patients with severe renal impairment. This will be determined by a creatinine clearance \< 70 ml/min/1.73 m2 (or serum creatinine \> 1.5 x Normal) or by a glomerular filtration rate \< 30% of predicted normal for age
  • Inadequate cardiac function as determined by fractional shortening \< 28% on echocardiogram, and/or ejection fraction of \< 50% on echocardiogram or RNCA.
  • Patients with FS of 23-28% who show an increase in FS in response to stress on the supine bicycle ergometer are eligible
  • Major liver dysfunction: SGOT \> 3 x upper limit of normal. Hyperbilirubinemia will not be used as an exclusion criteria because of the hemolytic component of the bilirubin. Patients with active hepatitis or severe liver fibrosis will also be excluded
  • Severe residual functional neurologic impairment
  • Stage III-IV sickle chronic lung disease
  • Pregnant or lactating women are excluded

Outcomes

Primary Outcomes

Define the role of bone marrow transplantation for the treatment of sickle cell disease and the reversibility of sickle cell vasculopathy and organ damage, good risk thalassemia major and Diamond-Blackfan Anemia.

Time Frame: 2 years

Study Sites (1)

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