Phase 3
N=22
Stem Cell Transplant for Hemoglobinopathy
Sickle Cell Disease · Thalassemia · Severe Congenital Neutropenia · Diamond-Blackfan Anemia · Shwachman-Diamond Syndrome
Bottom Line
View on ClinicalTrials.gov: NCT00176852 ↗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
| Outcome | Result | p-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
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.