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| Sponsor: | Masonic Cancer Center, University of Minnesota |
|---|---|
| Collaborator: |
National Marrow Donor Program |
| Information provided by: | Masonic Cancer Center, University of Minnesota |
| ClinicalTrials.gov Identifier: | NCT00176852 |
Purpose
This study tests the clinical outcomes of one of two preparative regimens (determined by available donor source) in patients with non-malignant hemoglobinopathies. The researchers hypothesize that these regimens will have a positive effect on post transplant engraftment and the incidence of graft-versus-host-disease.
Regimen A2 has replaced Regimen A in this study. Two patients were treated on Regimen A but did not have evidence of initial engraftment thus triggering the stopping rule for that arm of this study.
| Condition | Intervention | Phase |
|---|---|---|
|
Sickle Cell Disease Thalassemia Severe Congenital Neutropenia Diamond-Blackfan Anemia Shwachman-Diamond Syndrome |
Drug: Busulfan, Fludarabine, ATG, TLI Drug: Busulfan, Cyclophosphamide, ATG, GCSF Drug: Campath, Fludarabine, Cyclophosphamide Radiation: Total Body Irradiation Procedure: Stem cell infusion |
Phase II Phase III |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Allogeneic Hematopoietic Stem Cell Transplant for Patients With High Risk Hemoglobinopathy Using a Preparative Regimen to Achieve Stable Mixed Chimerism |
| Estimated Enrollment: | 30 |
| Study Start Date: | June 2002 |
| Estimated Study Completion Date: | June 2014 |
| Estimated Primary Completion Date: | June 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Regimen A - Full Prep (Discontinued)
Full Preparative Regimen for subjects with matched donors. Busulfan 0.8 mg/kg/dose intravenous (IV) Days -8 and -7, Fludarabine 35 mg/m2 IV Days -6 through -2, antithymocyte globulin (ATG) 30 mg/kg IV Days -2 through -1, total lymphoid radiation (TLI) Day -1, stem cell infusion on Day 0.
|
Drug: Busulfan, Fludarabine, ATG, TLI
Busulfan 0.8 mg/kg/dose intravenous (IV) Days -8 and -7 Fludarabine 35 mg/m2 IV Days -6 through -2 Antithymocyte globulin (ATG) 30 mg/kg IV Days -2 and -1 Total lymphoid radiation 300 cGy
Other Names:
|
|
Experimental: Regimen B - Myeloablative
Myeloablative Preparative Regimen for subjects with HLA identical sibling donors. Receives Busulfan 0.8 mg/kg/dose intravenous (IV) Days -9 through -6, Cyclophosphamide 50 mg/kg IV Days -5 through -2, ATG 30 mg/kg IV Day -1, stem cell infusion on Day 0 and G-CSF 5mcg/kg/day IV until ANC >2500 x 2 days.
|
Drug: Busulfan, Cyclophosphamide, ATG, GCSF
Busulfan 0.8 mg/kg/dose intravenous (IV) Days -9 through -6 Cyclophosphamide 50 mg/kg IV Days -5 through -2 ATG 30 mg/kg IV Day -1 GCSF 5 mcg/kg/day IV until ANC >2500 x 2 days.
Other Names:
Radiation: Total Body Irradiation
300 cGY Day -1
Other Name: TBI
Procedure: Stem cell infusion
Given Day 0
Other Name: bone marrow transplant
|
|
Experimental: Regimen A2 - Non-myeloablative
Receives Campath-1H 0.2 mg/kg Days -10 through -6, Cyclophosphamide 50 mg/kg I Day -7, Fludarabine 35 mg/m2 intravenous (IV) Days -6 through -2, total body irradiation (TBI) 300 cGy Day -1, stem cell infusion on Day 0. Regimen A2 will be utilized for patients with sickle cell disease or thalassemia who do not have an HLA-identical sibling donor or for any patient who has pre-existing organ dysfunction making them ineligible for a myeloablative preparative regimen. |
Drug: Campath, Fludarabine, Cyclophosphamide
Receives Campath-1H 0.2 mg/kg Days -10 through -6, Fludarabine 35 mg/m2 intravenous (IV) Days -6 through -2, total body irradiation (TBI) 300 cGy Day -1.
Other Names:
Radiation: Total Body Irradiation
300 cGY Day -1
Other Name: TBI
Procedure: Stem cell infusion
Given Day 0
Other Name: bone marrow transplant
|
Prior to transplantation, subjects will receive either:
Cyclophosphamide, Fludarabine, Campath, Total body irradiation (TBI)
Or
Busulfan, Cyclophosphamide, antithymocyte globulin (ATG), granulocyte colony-stimulating factor (GSCF)
These drugs (and the radiation) are being given to help the new stem cells take and grow. On the day of transplantation, subjects will receive stem cells transfused via intravenous (IV) catheter.
After stem cell transplantation, subjects will be given cyclosporine-A and mycophenolate (MMF)/or Methylprednisone/or Methotrexate to reduce the risk of graft-versus-host disease, the complication that occurs when the donor's stem cells react against the patient.
Eligibility| Ages Eligible for Study: | up to 50 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Patients with Sickle Cell Disease/Thalassemia (SCD/THAL) 0-50 years of age with an acceptable stem cell donor and disease characteristic defined by the following:
Second Transplants
Exclusion Criteria:
Contacts and Locations| Contact: Timothy Krepski, RN | 612-273-2800 | tkrepsk1@fairview.org |
| United States, Minnesota | |
| Masonic Cancer Center, University of Minnesota | Recruiting |
| Minneapolis, Minnesota, United States, 55455 | |
| Contact: Tim Krepski, RN 612-273-2800 tkrepsk1@fairiview.org | |
| Principal Investigator: Angela Smith, MD | |
| Principal Investigator: | Angela Smith, MD | Masonic Cancer Center, University of Minnesota |
More Information
| Responsible Party: | Smith, Angela R, Masonic Cancer Center, University of Minnesota |
| ClinicalTrials.gov Identifier: | NCT00176852 History of Changes |
| Obsolete Identifiers: | NCT00005897 |
| Other Study ID Numbers: | MT2002-07, 0206M26241 |
| Study First Received: | September 12, 2005 |
| Last Updated: | August 16, 2011 |
| Health Authority: | United States: Institutional Review Board |
|
high risk hemoglobinopathy stem cell transplant donor lymphocyte infusion transfusion dependent |
stem cell donor cord blood marrow transfusion dependent non-malignant hematologic disorders |
|
Anemia Anemia, Sickle Cell Hemoglobinopathies Neutropenia Thalassemia Bone Marrow Diseases Lipomatosis Exocrine Pancreatic Insufficiency Anemia, Diamond-Blackfan Hematologic Diseases Anemia, Hemolytic, Congenital Anemia, Hemolytic Genetic Diseases, Inborn Agranulocytosis Leukopenia |
Leukocyte Disorders Skin Diseases Lipid Metabolism Disorders Metabolic Diseases Pancreatic Diseases Digestive System Diseases Anemia, Hypoplastic, Congenital Anemia, Aplastic Red-Cell Aplasia, Pure Antilymphocyte Serum Busulfan Cyclophosphamide Fludarabine monophosphate Lenograstim Fludarabine |