Acquired Aplastic Anemia Clinical Trial
Official title:
Haploidentical Stem Cell Transplantation With Fixed Dose of T Cells After in Vitro T Cell Depletion Using CD3 Monoclonal Antibody for Children With Acquired Severe Aplastic Anemia
Rationale: Fludarabine, cyclophosphamide, anti-thymocyte globulin and low-dose total body
irradiation (LD-TBI) may induce the engraftment cross the immunologic barrier in the setting
of HLA-haploidentical allogeneic hematopoietic cell transplantation. In addition, depletion
of CD3 cells may contribute to prevent developing severe acute graft versus host disease
(GVHD) in haploidentical transplantation.
Purpose: Phase II trials to evaluate the efficacy of haploidentical stem cell
transplantation with fixed dose of T cells after in vitro T cell depletion using CD3
monoclonal antibody for children with acquired severe aplastic anemia
Status | Recruiting |
Enrollment | 10 |
Est. completion date | December 2015 |
Est. primary completion date | December 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A to 21 Years |
Eligibility |
Inclusion Criteria: - Diagnosis of life-threatening marrow failure (severe aplastic anemia) of nonmalignant etiology meeting 2 of the following criteria: - Granulocyte count < 500/mm3, - Corrected reticulocyte count < 1%, - Platelet count < 20,000/mm3 - No HLA-identical family member or closely matched (8 of 8 HLA-locus match) unrelated marrow donor available - HLA-haploidentical related donor available Exclusion Criteria: - Paroxysmal nocturnal hemoglobinuria or Fanconi anemia - Clonal cytogenetic abnormalities or myelodysplastic syndromes - Active fungal infections - HIV positive - Severe disease other than aplastic anemia that would severely limit the probability of survival during the graft procedure - Pregnant or nursing |
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Asan Medical Center | Seoul |
Lead Sponsor | Collaborator |
---|---|
Asan Medical Center |
Korea, Republic of,
Burroughs LM, Woolfrey AE, Storer BE, Deeg HJ, Flowers ME, Martin PJ, Carpenter PA, Doney K, Appelbaum FR, Sanders JE, Storb R. Success of allogeneic marrow transplantation for children with severe aplastic anaemia. Br J Haematol. 2012 Jul;158(1):120-8. doi: 10.1111/j.1365-2141.2012.09130.x. Epub 2012 Apr 26. — View Citation
Koh KN, Im HJ, Kim BE, Choi ES, Jang S, Kwon SW, Park CJ, Seo JJ. Haploidentical haematopoietic stem cell transplantation using CD3 or CD3/CD19 depletion and conditioning with fludarabine, cyclophosphamide and antithymocyte globulin for acquired severe ap — View Citation
Tolar J, Deeg HJ, Arai S, Horwitz M, Antin JH, McCarty JM, Adams RH, Ewell M, Leifer ES, Gersten ID, Carter SL, Horowitz MM, Nakamura R, Pulsipher MA, Difronzo NL, Confer DL, Eapen M, Anderlini P. Fludarabine-based conditioning for marrow transplantation from unrelated donors in severe aplastic anemia: early results of a cyclophosphamide dose deescalation study show life-threatening adverse events at predefined cyclophosphamide dose levels. Biol Blood Marrow Transplant. 2012 Jul;18(7):1007-11. doi: 10.1016/j.bbmt.2012.04.014. Epub 2012 Apr 27. — View Citation
Xu LP, Liu KY, Liu DH, Han W, Chen H, Chen YH, Zhang XH, Wang Y, Wang FR, Wang JZ, Huang XJ. A novel protocol for haploidentical hematopoietic SCT without in vitro T-cell depletion in the treatment of severe acquired aplastic anemia. Bone Marrow Transplant. 2012 Dec;47(12):1507-12. doi: 10.1038/bmt.2012.79. Epub 2012 May 28. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To assess engraftment rate and survival of haploidentical stem cell transplantation with fixed dose of T cells after in vitro T cell depletion using CD3 monoclonal antibody for children with acquired severe aplastic anemia | 2 years posttransplant | Yes | |
Secondary | To assess engraftment and graft failure | Number of patients who failed to engraft by 28 days | 28 days posttransplant | Yes |
Secondary | To estimate the risk of acute GVHD | Number of patients with acute GVHD. | 100 days posttransplant | Yes |
Secondary | To assess treatment related mortality | Number of death after transplantation | 100 days posttransplant | Yes |
Secondary | To estimate overall survival and failure free survival | 1 year posttransplant | No |
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