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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
26
Day 9 before BMT: 0.5mg/kg IV; Days 8 \& 7 before BMT: 2mg/kg IV Days 8 \& 7 - 2mg/kg IV before BMT
Days 6 and 2 before BMT: 30mg/m2/day IV
Days 6 and 5 before BMT: 14.5mg/kg IV; Days 3 and 4 after BMT: 50mg/kg/day
Days 3 \& 4 after BMT: 40 mg/kg IV
Adjusted to maintain a serum trough level of 3-12 ng/mL, taken orally beginning on 5 days after BMT and taken to 1 year after BMT.
15 mg/kg orally with maximum dose 3 mg/day beginning 5 days after BMT and taken to day 35 after BMT
Day 0 - Transplantation of hematopoietic cells derived from bone marrow of a donor to a recipient as treatment for hematologic disorders
200 cGy on the day before BMT. Radiation delivered to the entire body of the recipient to eradicate bone marrow cells in the recipient to prepare the recipient to receive the transplanted
Vanderbilt-Ingram Cancer Center
Nashville, Tennessee, United States
Saint-Louis Hospital
Paris, France
St Mary's Hospital
London, United Kingdom
Transplant-related Mortality (TRM)
Defined as death in the absence of recurrent sickle cell disease or hemoglobinopathy
Time frame: at 1 year after BMT
Number of Patients Who Developed Grade I-IV Acute Graft-vs.-Host Disease
GVHD Severity was graded using the established National Institutes of Health's consensus criteria \[36\].
Time frame: 2 years
Number of Patients With Donor Hematopoietic Chimerism in Peripheral Blood <95% at 6 Months After Mini-haploBMT
Partially human leukocyte antigen (HLA)-mismatched bone marrow from first-degree relatives. Defined in percentages of donor cells in patient's peripheral blood, measured in 4 ways. * Mixed donor chimerism: \> 0% but \< 95% * Complete donor chimerism \> 95% Any amount of donor chimerism after day 60 will be considered as having engrafted
Time frame: Up to approximately 180 after mini-haploBMT
Number of Participants With Hematologic and Non-hematologic Toxicities Following minihaploBMT
Hematologic toxicity: -Absolute neutrophil count (ANC): consecutive values of \< 500/µL on 3 different days after chemotherapy post-BMT Platelet count: consecutive values of \< 20,000 µL on 3 different days after chemotherapy post-BMT Non-hematologic toxicities: -Toxicities necessitating hospitalization Toxicities grade 4 or above Meets the criteria of the following SAE: * Relapse of underlying disease * Grade 3 ocular toxicity not related to ocular GVHD * Grade 3 related non-hematologic toxicity
Time frame: Day 60 after BMT
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