A Phase 1/2 interventional study of Autologous hematopoietic stem cell transplantation and Allogeneic stem cell transplantation in Sarcoidosis, sponsored by Northwestern University. Terminated at 1 site in United States. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2018-08-31.
Sponsored by Northwestern University · Phase 1/2, Interventional, and Treatment
Sarcoidosis is a disease believed to be due to immune cells, cells which normally protect the body, but are now attacking lungs, heart, nerves, or other organs or systems within the body. As a result, the affected organs or systems fail to work properly causing difficulty breathing; heart failure; inability of the nerves to respond properly causing numbing, tingling, pain, and progressive muscle weakness; or other symptoms depending on the organ or body system involved. The likelihood of progression of this disease is high. This study is designed to examine whether treating patients with high dose cyclophosphamide (a drug which reduces the function of the immune system) and ATG (a protein that kills the immune cells that are thought to be causing this disease), followed by return of the previously collected blood stem cells will stop the progression of sarcoidosis. Stem cells are undeveloped cells that have the capacity to grow into mature blood cells, which normally circulate in the blood stream. The purpose of the high dose cyclophosphamide and ATG is to destroy the cells in the immune system. The purpose of the stem cell infusion is to evaluate whether this treatment will produce a normal immune system that will no longer attack the body.
Method of Harvesting Stem Cells
Based on the experience of the pilot studies, the current protocol will mobilize stem cells with granulocyte-colony stimulating factor (G-CSF) and collect stem cells by apheresis, with subsequent bone marrow harvest performed only if needed to supplement the peripheral blood stem cells (PBSC). Based on experience of autoimmune flares in patients receiving G-CSF alone for mobilization, patients will be mobilized with cyclophosphamide 2.0 g/m2 and G-CSF 10 mcg/kg.
Cyclophosphamide
Cyclophosphamide (CY) is an active agent in patients with a wide variety of malignancies. It is used frequently in the therapy of lymphoid malignancies and has potent immunosuppressive activity. It is frequently used as a cytotoxic and immunosuppressive agent in patients undergoing marrow transplants and as a treatment for patients with autoimmune diseases. It is an alkylating agent that requires hepatic metabolism to the active metabolites, phosphoramide mustard and acrolein. These active metabolites react with nucleophilic groups. It is available as an oral or intravenous preparation. Bioavailability is 90% when given orally. The half-life of the parent compound is 5.3 hours in adults, and the half-life of the major metabolite phosphoramide mustard is 8.5 hours. Liver or renal dysfunction will lead to prolonged serum half-life. CY is administered intravenously at a dosage of 60 mg/kg on each of 2 successive days (use adjusted ideal body weight if patient's actual body weight is greater than 100% ideal body weight). The major dose limiting side effect at high doses is cardiac necrosis. Hemorrhagic cystitis can occur and is mediated by the acrolein metabolite. This can be prevented by co-administration of MESNA or bladder irrigation. Other notable side effects include nausea, vomiting, alopecia, myelosuppression and SIADH. Refer to institutional manuals for more information about administration, toxicity and complications.
Rabbit-Derived Anti-Thymocyte Globulin (ATG)
Rabbit-derived anti-human thymocyte globulin (ATG) is a gamma globulin preparation obtained from hyperimmune serum of rabbits immunized with human thymocytes. ATG has been used predominately in solid organ transplant immunosuppressive regimens. ATG is a predominantly lymphocyte-specific immunosuppressive agent. It contains antibodies specific to the antigens commonly found on the surface of T cells. After binding to these surface molecules, ATG promotes the depletion of T cells from the circulation through mechanisms, which include opsonization and complement-assisted, antibody-dependent, cell-mediated cytotoxicity. The plasma half-life ranges from 1.5 12 days. ATG is administered intravenously at a dose of 0.5-mg/kg recipient body weight on day -6 and at a dose of 1.0 mg/kg recipient body weight on days -5 to -1. Unlike equine ATG, rabbit ATG does not require a pre-infusion skin test to check for hypersensitivity. Methylprednisolone 250mg (dose adjusted based on patient's condition) will be given before every dose of ATG. Additional medications such as diphenhydramine may be given at the discretion of the attending physician. Although rare, the major toxicity is anaphylaxis; chills, fever, pruritus or serum sickness may occur.
Fludarabine
Fludarabine phosphate is rapidly dephosphorylated to 2-fluoro-ara-A and then phosphorylated intracellularly by deoxycytidine kinase to the active triphosphate, 2-fluoro-ara-ATP. This metabolite appears to act by inhibiting DNA polymerase alpha, ribonucleotide reductase and DNA primase, thus inhibiting DNA synthesis. The mechanism of action of this antimetabolite is not completely characterized and may be multi-faceted.
Phase I studies in humans have demonstrated that fludarabine phosphate is rapidly converted to the active metabolite, 2-fluoro-ara-A, within minutes after intravenous infusion. Consequently, clinical pharmacology studies have focused on 2-fluoro-ara-A pharmacokinetics. After the five daily doses of 25 mg 2-fluoro-ara-AMP/m2 to cancer patients infused over 30 minutes, 2-fluoro-ara-A concentrations show a moderate accumulation. During a 5-day treatment schedule, 2-fluoro-ara-A plasma trough levels increased by a factor of about 2. The terminal half-life of 2-fluoro-ara-A was estimated as approximately 20 hours. In vitro, plasma protein binding of fludarabine ranged between 19% and 29%.
CAMPATH
Campath-1H is a humanized fusion protein that is directed to CD52 antigen that is expressed on all lymphocytes, monocytes and macrophages. It has very potent immunosuppressive property and is effective for prevention of graft-versus-host disease. 30 mg/day of CAMPATH will be given intravenously over 2 hours on days -4, -3 and -2. The most commonly reported adverse reactions are infusion reactions fever, chills, hypotension, urticaria, nausea, rash, tachycardia, dyspnea), cytopenias (neutropenia, lymphopenia, thrombocytopenia, anemia), and infections (CMV viremia, CMV infection, other infections). In clinical trials, the frequency of infusion reactions was highest in the first week of treatment. Other commonly reported adverse reactions include vomiting, abdominal pain, insomnia and anxiety. The most commonly reported serious adverse reactions are cytopenias, infusion reactions, and immunosuppression/infections. About 30 minutes before the patient gets Campath, he/she will be given other medications (such as acetaminophen or diphenhydramine, given orally, not IV) to help reduce side effects.
278 studies on the registry are indexed under Sarcoidosis; 57 are open to participants now.
This study's enrollment of 2 is below the median of 54 across 154 interventional studies indexed under Sarcoidosis.
Browse Sarcoidosis studies →Northwestern University is the lead sponsor of 1,396 studies on the registry; 199 are open to participants now.
Of its 102 completed or terminated interventional studies of FDA-regulated products, 73 (72%) have results posted.
Counted across the registry records on this site, refreshed daily.
Failure of therapy defined by (not caused by unrelated conditions) any one of following:
Persistent peripheral neuropathy (one of following):
Exclusion Criteria:
Significant end organ damage such as:
Autologous stem cells will be injected after conditioning
Biological: Autologous hematopoietic stem cell transplantation
Allogeneic stem cells will be injected after conditioning
Biological: Allogeneic stem cell transplantation
Autologous hematopoietic stem cells will be injected after conditioning
Also known as: Autologous stem cell injection
Allogeneic stem cells will be injected after conditioning
Presence of Toxicity
Daily assessment will be made with regards to toxicity by one of the protocol investigators.National Cancer Institute Common Toxicity Criteria will be used to grade all non-hematologic toxicities. Toxicity grades as follows: 1 = Mild; 2 = Moderate; 3 = Severe and undesirable; 4 = life threatening or disabling ; 5 = Death
Time frame: For length of hospital stay (until discharge).
Survival
Patient has not died.
Time frame: Participants are to be followed at 6 months and then yearly until 5 years
Time to Disease Progression
Worsening symptoms, pulmonary function studies, cardiac function and arrhythmia including EKG assessments, and neurological symptoms.
Time frame: Participants are to be followed at 6 months and then yearly until 5 years
| Milestone | Autologous Hematopoietic Stem Cell Transplantation | Allogeneic Stem Cell Transplantation |
|---|---|---|
| Started | 1 | 1 |
| Completed | 0 | 0 |
| Not completed | 1 | 1 |
| Withdrew: Lack of efficacy | 1 | 0 |
| Withdrew: Death | 0 | 1 |
Daily assessment will be made with regards to toxicity by one of the protocol investigators.National Cancer Institute Common Toxicity Criteria will be used to grade all non-hematologic toxicities. Toxicity grades as follows: 1 = Mild; 2 = Moderate; 3 = Severe and undesirable; 4 = life threatening or disabling ; 5 = Death
| participants | Autologous Hematopoietic Stem Cell Transplantation | Allogeneic Stem Cell Transplantation |
|---|---|---|
| Presence of Toxicity | 1 | 1 |
Patient has not died.
| Participants | Autologous Hematopoietic Stem Cell Transplantation | Allogeneic Stem Cell Transplantation |
|---|---|---|
| Survival | 1 | 0 |
Worsening symptoms, pulmonary function studies, cardiac function and arrhythmia including EKG assessments, and neurological symptoms.
| months | Autologous Hematopoietic Stem Cell Transplantation | Allogeneic Stem Cell Transplantation |
|---|---|---|
| Time to Disease Progression | 4 | 0 |
Collected over Adverse event data was collected from time of first transplant 4/25/2012 until patient death 6/27/2015. Study closure effective 8/17/2015.. Non-serious events are listed at a 0% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Autologous Hematopoietic Stem Cell Transplantation | — | 0/1 (0%) | 0/1 (0%) |
| Allogeneic Stem Cell Transplantation | — | 1/1 (100%) | 0/1 (0%) |
| Event | Autologous Hematopoietic Stem Cell Transplantation | Allogeneic Stem Cell Transplantation |
|---|---|---|
| DeathInfections and infestations | 0/1 | 1/1 |
| SepsisInfections and infestations | 0/1 | 1/1 |
| Age, Categorical(Participants) | Autologous Hematopoietic Stem Cell Transplantation | Allogeneic Stem Cell Transplantation | Total |
|---|---|---|---|
| <=18 years | 0 | 0 | 0 |
| Between 18 and 65 years | 1 | 1 | 2 |
| >=65 years | 0 | 0 | 0 |
| Age, Continuous(years) | Autologous Hematopoietic Stem Cell Transplantation | Allogeneic Stem Cell Transplantation | Total |
|---|---|---|---|
| Mean | 54 ± NA | 49 ± NA | 51.5 ± 2.5 |
| Sex: Female, Male(Participants) | Autologous Hematopoietic Stem Cell Transplantation | Allogeneic Stem Cell Transplantation | Total |
|---|---|---|---|
| Female | 0 | 1 | 1 |
| Male | 1 | 0 | 1 |
| Region of Enrollment(participants) | Autologous Hematopoietic Stem Cell Transplantation | Allogeneic Stem Cell Transplantation | Total |
|---|---|---|---|
| United States | 1 | 1 | 2 |
Plan to share: Undecided
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