A Non-Myeloablative Conditioning and Transplantation of Partially HLA-Mismatched and HLA-Matched Bone Marrow for Patients With Sickle Cell Disease and Other Hemoglobinopathies
Overview
- Phase
- Not Applicable
- Intervention
- Thymoglobulin
- Conditions
- Sickle Cell Disease
- Sponsor
- Vanderbilt-Ingram Cancer Center
- Enrollment
- 26
- Locations
- 3
- Primary Endpoint
- Transplant-related Mortality (TRM)
- Status
- Active, not recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
Allogeneic blood or marrow transplantation (alloBMT) is a curative therapy for a variety of hematologic disorders, including sickle cell disease and thalassemia. Even when it is clear that alloBMT can give to these patients an improvement in their disease, myeloablative transplants have important toxicities and mortalities associated. The lack of suitable donors continues to be a limit to access to transplantation. Substantial progress has been made recently in the development of pre-treatment regimens that facilitate the sustained engraftment of donor marrow with reduced toxicity. Most of these regimens incorporate highly immunosuppressive drugs, which allow the reduction or elimination of myeloablative agents or total body irradiation without endangering the sustained engraftment of HLA-identical allogeneic stem cells. Preliminary results of non-myeloablative allogeneic stem cell transplantation suggest that the procedure can be performed in patients who are ineligible for myeloablative alloBMT, and that sustained remissions of several hematologic malignancies can be obtained.
Investigators
Adetola A. Kassim
Professor of Medicine; Clinical Director, Sickle Cell Anemia Program; Medical Oncologist
Vanderbilt-Ingram Cancer Center
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Arms & Interventions
Non-Myeloablative Conditioning and Bone Marrow Transplantation
Intervention: Thymoglobulin
Non-Myeloablative Conditioning and Bone Marrow Transplantation
Intervention: Fludarabine
Non-Myeloablative Conditioning and Bone Marrow Transplantation
Intervention: Cyclophosphamide (CTX)
Non-Myeloablative Conditioning and Bone Marrow Transplantation
Intervention: Mesna
Non-Myeloablative Conditioning and Bone Marrow Transplantation
Intervention: Sirolimus
Non-Myeloablative Conditioning and Bone Marrow Transplantation
Intervention: Mycophenolate mofetil (MMF)
Non-Myeloablative Conditioning and Bone Marrow Transplantation
Intervention: Bone marrow transplantation
Non-Myeloablative Conditioning and Bone Marrow Transplantation
Intervention: Total body irradiation
Outcomes
Primary Outcomes
Transplant-related Mortality (TRM)
Time Frame: at 1 year after BMT
Defined as death in the absence of recurrent sickle cell disease or hemoglobinopathy
Secondary Outcomes
- Number of Patients Who Developed Grade I-IV Acute Graft-vs.-Host Disease(2 years)
- Number of Patients With Donor Hematopoietic Chimerism in Peripheral Blood <95% at 6 Months After Mini-haploBMT(Up to approximately 180 after mini-haploBMT)
- Number of Participants With Hematologic and Non-hematologic Toxicities Following minihaploBMT(Day 60 after BMT)