Haploidentical Allogeneic Hematopoietic Stem Cell Transplantation (HaploHCT) Following Reduced Intensity Conditioning (RIC) for Selected High Risk Non-Malignant Diseases
Sickle Cell Disease, Thalassemia, High Risk Hematologic Disorders
About this trial
This is an interventional treatment trial for Sickle Cell Disease focused on measuring SCD, cALD
Eligibility Criteria
Inclusion Criteria:
Sickle Cell Disease (SCD)
* If diagnosis of SCD must meet one or more of the following disease characteristics:
- Stroke, CNS hemorrhage or a neurologic event lasting longer than 24 hours, or abnormal cerebral MRI or cerebral arteriogram or MRI angiographic study and impaired neuropsychological testing
- Acute chest syndrome with a history of recurrent hospitalizations or exchange transfusions
- Recurrent vaso-occlusive pain 3 or more episodes per year for 3 years or more years or recurrent priapism,
- Impaired neuropsychological function and abnormal cerebral MRI scan
- Stage I or II sickle lung disease,
- Sickle nephropathy (moderate or severe proteinuria or a glomerular filtration rate [GFR] 30-50% of the predicted normal value)
- Bilateral proliferative retinopathy and major visual impairment in at least one eye
- Osteonecrosis of multiple joints with documented destructive changes
- Requirement for chronic transfusions
- RBC alloimmunization
- Transfusion Dependent Alpha- or Beta-Thalassemia
- Other Non-Malignant Hematologic Disorders:
Transfusion dependent or involve other potential life-threatening cytopenias, including but not limited to Paroxysmal Nocturnal Hemoglobinuria, Glanzmann's Thrombasthenia, Severe Congenital Neutropenia and Shwachman-Diamond Syndrome
cALD
- Diagnosis of ALD by abnormal plasma very long chain fatty acid (VLCFA) profile or ABCD1 gene mutation
- Cerebral disease on MRI
- Absence of a Major Functional Disability (cortical blindness, loss of communication, wheelchair dependence) on the ALD Neurologic Function Scale
- Other inherited metabolic disorders:
Any other inherited metabolic disorder for which alloHCT is indicated and for whom, in the opinion of the treating physician, the patient's best treatment option is with a haploidentical donor following non-myeloablatve conditioning.
Age, Performance Status, Consent
- Age: 0-55 years
- Performance Status: Karnofsky ≥ 70%, Lansky play score ≥ 70
- Consent: voluntary written consent (adult or parental/guardian)
Adequate Organ Function
- Renal: Creatinine <2.0 mg/dl for adults or glomerular filtration rate > 50 ml/min for children
- Hepatic: Bilirubin and ALT <3 times the upper limit of institutional normal
- Cardiac: Absence of decompensated congestive heart failure, or uncontrolled arrhythmia and left ventricular ejection fraction > 40%.
Exclusion Criteria:
- Availability of a suitable HLA-matched related donor
- Uncontrolled infection
- Pregnant or breastfeeding
- HIV positive
Sites / Locations
- Masonic Caner Center at University of Minnesota
Arms of the Study
Arm 1
Experimental
rATG, FLU/CY/TBI, & Thiotepa
Anti-Thymocyte Globulin - Rabbit (rATG), Fludarabine (Fludara), Cyclophosphamide (Cytoxan, Neosar), Total Body Irradiation (TBI), & Thiotepa