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Phase 3 N=22 Treatment

Stem Cell Transplant for Hemoglobinopathy

Sickle Cell Disease · Thalassemia · Severe Congenital Neutropenia · Diamond-Blackfan Anemia · Shwachman-Diamond Syndrome

Enrolled (actual)
22
Serious AEs
9.1%
Results posted
May 2017
Primary outcome: Primary: Number of Patients Who Experienced Grade 3-5 Treatment Related Toxicity — 0; 0; 2 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Busulfan, Fludarabine, ATG, TLI (Drug); Busulfan, Cyclophosphamide, ATG, GCSF (Drug); Campath, Fludarabine, Cyclophosphamide (Drug); Total Body Irradiation (Radiation); Stem cell infusion (Procedure)
Age
Pediatric, Adult
Sex
All
Sponsor
Masonic Cancer Center, University of Minnesota
Primary completion
Mar 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Patients Who Experienced Grade 3-5 Treatment Related Toxicity
0; 0; 2
SECONDARY
The Incidence of Chimerism at 100 Days
1; 5; 11
SECONDARY
The Incidence of Chimerism at 6 Months
1; 5; 8
SECONDARY
The Incidence of Chimerism at 1 Year
1; 5; 8
SECONDARY
The Incidence of Grade 2-4 Acute Graft Versus Host Disease (Acute GVHD)
0; 0; 0
SECONDARY
The Incidence of Grade 3-4 Acute Graft Versus Host Disease (Acute GVHD)
0; 0; 0
SECONDARY
The Incidence of Chronic Graft Versus Host Disease (Chronic GVHD)
0; 0; 0
SECONDARY
The Incidence of Chronic Graft Versus Host Disease (Chronic GVHD)
0; 0; 0
SECONDARY
Change in the Patient's Quality of Life as Compared to the Pre-Transplant Assessment
100; 100; 100
SECONDARY
Change in the Patient's Quality of Life as Compared to the Pre-Transplant Assessment
100; 100; 100
SECONDARY
Change in the Patient's Quality of Life as Compared to the Pre-Transplant Assessment
100; 100; 100
SECONDARY
Determine Physical Characteristics and Biologic Effects of Mixed Populations of Donor and Host Red Blood Cells
SECONDARY
Determine the Concentration of Campath in the Serum
SECONDARY
Overall Survival
3; 5; 12
SECONDARY
Overall Survival
3; 5; 12
SECONDARY
Disease Free Survival
3; 5; 11
SECONDARY
Disease Free Survival
3; 5; 11

Summary

This study tests the clinical outcomes of one of two preparative regimens (determined by available donor source) in patients with non-malignant hemoglobinopathies. The researchers hypothesize that these regimens will have a positive effect on post transplant engraftment and the incidence of graft-versus-host-disease. Regimen A2 has replaced Regimen A in this study. Two patients were treated on Regimen A but did not have evidence of initial engraftment thus triggering the stopping rule for that arm of this study.

Eligibility Criteria

Inclusion Criteria

  • Patients with Sickle Cell Disease/Thalassemia (SCD/THAL) 0-50 years of age with an acceptable stem cell donor and disease characteristic defined by the following:
  • Stroke, central nervous system (CNS) hemorrhage or a neurologic event lasting longer than 24 hours, or abnormal cerebral magnetic resonance imaging (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 but with red blood cell (RBC) alloimmunization >2 antibodies during long term transfusion therapy
  • Patients with transfusion dependent alpha- or beta-thalassemia 0-35 years of age with an acceptable stem cell donor as defined in the criteria in section above.
  • Patients with other non-malignant hematologic disorders that are transfusion-dependent or involve other potentially life-threatening cytopenias (including but not limited to Severe Congenital Neutropenia, Diamond-Blackfan Anemia and Shwachman-Diamond Syndrome) who are 0-35 years of age with an acceptable stem cell donor
  • Second Transplants
  • Patients with sickle cell disease or thalassemia who have failed to engraft or have autologous recovery after a myeloablative SCT regimen or non-myeloablative regimen are eligible for this protocol.
  • Regimen A2 will be utilized for patients with sickle cell disease or thalassemia who do not have an HLA-identical sibling donor or for any patient who has pre-existing organ dysfunction making them ineligible for a myeloablative preparative regimen.
  • Regimen B will be utilized for patients with sickle cell disease or thalassemia who have an HLA-identical sibling donor.
  • Patients must meet above criteria.
  • If the patient has received prior radiation therapy, eligibility to receive additional radiation therapy must be determined by Dr. Dusenbery
  • If first transplant was a non-myeloablative regimen, the second transplant can occur at any time
  • If the first transplant was a myeloablative regimen, then the second transplant must be > 6 months from the first transplant

Exclusion Criteria

  • Patients with one or more of the following:
  • Karnofsky or Lansky performance score <70
  • Acute hepatitis or evidence of moderate or severe portal fibrosis or cirrhosis on biopsy
  • Stage III-IV lung disease
  • GFR<30% predicted
  • Pregnant or lactating females
  • Active serious infection whereby patient has been on intravenous antibiotics for one week prior to study entry. Any patient with AIDS or ARC or HIV seropositivity
  • Psychologically incapable of undergoing bone marrow transplant (BMT) with associated strict isolation or documented history of medical non-compliance
  • Patients not able to receive total lymphocytic irradiation (TLI) due to prior radiation therapy
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00176852). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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