Pilot Study of Total Body Irradiation in Combination With Cyclophosphamide, Anti-thymocyte Globulin, and Autologous CD34-Selected Peripheral Blood Stem Cell Transplantation in Children With Refractory Autoimmune Disorders
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Purpose
OBJECTIVES: I. Determine the safety and long term complications of total body irradiation in combination with cyclophosphamide, anti-thymocyte globulin, and autologous CD34-selected peripheral blood stem cell (PBSC) transplantation in children with refractory autoimmune disorders.
II. Determine the efficacy of this treatment regimen in these patients. III. Determine the reconstitution of immunity after autologous CD34-selected PBSC transplantation in these patients.
IV. Determine engraftment of autologous CD34-selected PBSC in these patients.
| Condition | Intervention | Phase |
|---|---|---|
|
Systemic Sclerosis Systemic Lupus Erythematosus Dermatomyositis Juvenile Rheumatoid Arthritis Autoimmune Diseases |
Procedure: Stem Cell Transplantation |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Pilot Study of High-Dose Immunosuppression Followed by Infusion of CD34-Selected Autologous or Syngeneic Peripheral Blood Stem Cells for Treatment of Refractory Autoimmune Disorders |
- Mortality [ Time Frame: Annually for 5 years and then every 5 years thereafter ] [ Designated as safety issue: Yes ]
- Immune reconstitution, engraftment, efficacy, late-effects [ Time Frame: Annually for 5 years and then every 5 years thereafter ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 20 |
| Study Start Date: | November 2000 |
| Study Completion Date: | May 2011 |
| Primary Completion Date: | July 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
Participants will receive a stem cell transplant.
|
Procedure: Stem Cell Transplantation
Participants will receive a stem cell transplantation along with irradiation and the drugs anti-thymocyte globulin, cyclophosphamide, and filgrastim as noted in the text of this record.
|
Detailed Description:
PROTOCOL OUTLINE: This is a multicenter study. Patients receive filgrastim (G-CSF) subcutaneously daily until peripheral blood stem cell (PBSC) collection is completed. CD34+ cells are separated from the rest of the PBSCs.
Patients undergo total body irradiation twice daily on days -5 and -4. Patients receive anti-thymocyte globulin IV on days -5, -3, -1, 1, 3, and 5 and cyclophosphamide IV on days -3 and -2. CD34-selected PBSCs are reinfused on day 0. Patients receive G-CSF IV daily beginning on day 0 and continuing until blood counts recover.
Patients are followed annually for 5 years and then every 5 years thereafter.
Eligibility| Ages Eligible for Study: | 2 Years to 18 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
PROTOCOL ENTRY CRITERIA:
--Disease Characteristics--
- Diagnosis of 1 of the following based on American College of Rheumatology (ACR) Criteria: Severe juvenile rheumatoid arthritis (systemic onset or polyarticular course) Juvenile systemic lupus erythematosus Systemic sclerosis Dermatomyositis
- Refractory to standard or aggressive therapy OR unacceptable toxicity from standard therapy
- Reasonable expectation of possible improvement as evidenced by a good potential for rehabilitation therapy and adequate social factors
- No serious CNS damage that would preclude significant functional recovery
--Prior/Concurrent Therapy--
- Chemotherapy: At least 4 weeks since prior methotrexate or cyclophosphamide
- Endocrine therapy: At least 4 weeks since prior intra-arterial steroids Juvenile rheumatoid arthritis patients should continue steroids without taper throughout mobilization and harvest of stem cells If receiving corticosteroids, must be continued without taper
Other:
- At least 4 weeks since prior anti-inflammatory agents such as non-steroidal anti-inflammatory drugs (NSAIDs) or sulfasalazine
- At least 4 weeks since prior cyclosporine, tacrolimus, mycophenolate mofetil, azathioprine, penicillamine, or etanercept
--Patient Characteristics--
- Life expectancy: At least 30 days
- Hematopoietic: Absolute neutrophil count at least 1,000/mm3 OR Platelet count at least 100,000/mm3 No bone marrow aspirate or biopsy consistent with production defect (depletion of neutrophil precursors or megakaryocytes) No myelodysplasia
- Hepatic: Bilirubin no greater than 2.5 mg/dL AST no greater than 300 U/L on two sequential tests No severe liver dysfunction within past month No active hepatitis A, B, or C
- Renal: No end-stage glomerulonephritis or renal disease Creatinine clearance at least 40 mL/min
- Cardiovascular: No uncontrolled malignant arrhythmia No New York Heart Association class III or IV congestive heart failure Ejection fraction at least 50%
- Pulmonary: DLCO at least 45% (DLCO at least 70% for patients with pulmonary disease caused by documented processes other than primary autoimmune disorder, such as infectious pneumonia or aspiration pneumonia) No severe pulmonary hypertension (PAP greater than 50) without potential for significant improvement
Other:
- No medical or psychosocial reasons that would make hematopoietic stem cell collection intolerable
- No increased anesthetic risks
- No fever higher than 39 degrees C
- No positive serology for toxoplasmosis
- No active life threatening infection not responsive to therapy
- No other disease or organ dysfunction that would limit survival
- No known hypersensitivity to murine or equine proteins
- No known primary immunodeficiency disease HIV negative
Contacts and Locations| United States, Washington | |
| Fred Hutchinson Cancer Research Center | |
| Seattle, Washington, United States, 98109 | |
| Study Chair: | Ann Woolfrey | Fred Hutchinson Cancer Research Center |
| Principal Investigator: | Carol A. Wallace, MD | Fred Hutchinson Cancer Research Center |
More Information
No publications provided
| Responsible Party: | Ann E. Woolfrey, MD / Associate Member, Fred Hutchinson Cancer Research Center |
| ClinicalTrials.gov Identifier: | NCT00010335 History of Changes |
| Other Study ID Numbers: | 1353.00, FHCRC-1353.00, 199/15575 |
| Study First Received: | February 2, 2001 |
| Last Updated: | May 25, 2011 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Fred Hutchinson Cancer Research Center:
|
arthritis & connective tissue diseases dermatomyositis immunologic disorders and infectious disorders juvenile rheumatoid arthritis |
rare disease systemic lupus erythematosus systemic sclerosis |
Additional relevant MeSH terms:
|
Arthritis Arthritis, Rheumatoid Autoimmune Diseases Dermatomyositis Lupus Erythematosus, Systemic Scleroderma, Systemic Scleroderma, Diffuse Sclerosis Arthritis, Juvenile Rheumatoid Joint Diseases Musculoskeletal Diseases Rheumatic Diseases Connective Tissue Diseases Immune System Diseases Myositis |
Muscular Diseases Polymyositis Neuromuscular Diseases Nervous System Diseases Skin Diseases Pathologic Processes Antilymphocyte Serum Cyclophosphamide Immunosuppressive Agents Immunologic Factors Physiological Effects of Drugs Pharmacologic Actions Antirheumatic Agents Therapeutic Uses Antineoplastic Agents, Alkylating |
ClinicalTrials.gov processed this record on May 19, 2013