Alemtuzumab: Alemtuzumab, Day -7 to -3. Dose: 0.2mg/kg/dose SC once daily x 5 days
Total Body Irradiation: TBI 300 cGy on Day -2
Sirolimus: Sirolimus is used for GVHD prophylaxis
Study summary
The aim of this study to evaluate the safety and efficacy of a nonmyeloablative conditioning regimen for allogeneic hematopoietic stem cell transplantation (HSCT) in pediatric patients with sickle cell disease (SCD) who have a matched related major ABO-incompatible donor. The nonmyeloablative regimen will use alemtuzumab, total body irradiation (TBI) and sirolimus for immune suppression. This study will expand the access of HSCT for patients with SCD who are currently not eligible because of donor restrictions.
Eligibility
Sex
ALL
Min age
1 Year
Max age
19 Years
Healthy volunteers
No
Inclusion Criteria:
* Patients must be ≥ 12 months and \< 19 years of age at the time of study enrollment.
* Patients must have sickle cell disease as defined by hemoglobin electropheresis, as follows:
* homozygous Hb S disease (HbSS),
* sickle-Hb C disease (HbSC),
* sickle beta-plus-thalassemia (HbS/β+), or
* sickle beta-null-thalassemia (HbS/βo)
* Patients must meet standard eligibility criteria to undergo HSCT, including but not limited to one or more of the following:
* history of repeated (more than 1) bony (vaso-occlusive) crisis
* history of stroke
* elevated transcranial Doppler velocity not eligible for hydroxyurea, as per TWiTCH trial (ie. severe vasculopathy)
* history of acute chest crisis or splenic sequestration crisis
* history of priapism in males
* history of osteonecrosis
* pulmonary hypertension as documented by tricuspid regurgitation jet velocity (TRV) \> 2.5 m/s on echocardiogram
* red cell allo-immunization (≥ 2 antibodies) during long term transfusion therapy
* Sickle complications should be present despite the use of hydroxyurea, but this is not an absolute requirement, if the treating team considers the patient to be at high risk for further crisis episodes.
Exclusion Criteria:
* Patients who are unable to comply with or follow the study protocol.
* Patients with known hypersensitivity to sirolimus, its derivatives or to any of its components.
Primary outcome measure(s)
Incidence of pure red cell aplasia (PRCA) — 6 months from enrollment Clinical definition: reticulocytopenia \< 10x109/L (\< 1%) lasting more than 60 days after HSCT, or Pathological definition: the absence of erythroid precursors in the marrow in the setting of adequate myeloid, lymphoid and megakaryocytic precursors
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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