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Hematopoietic Stem Cell Support in Patients With Autoimmune Bullous Skin Disorders

Primary Purpose

Pemphigus

Status
Terminated
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Hematopoietic stem cell transplantation
Sponsored by
Richard Burt, MD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pemphigus

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Less than chronologic age 60 years at the time of pre-transplant evaluation. An established diagnosis of an autoimmune skin disorder that includes any of the following: pemphigus vulgaris pemphigus foliaceus Diagnosis of bullous skin lesions will be based on history and physical, skin biopsy (light microscopy and indirect fluorescence), indirect immunofluorescence titer, BP 180 and 230 titers, Desmolglein-3 and Desmoglein-1 antibody, and photograph. Patients who failed corticosteroids (equivalent dosage of prednisone 0.5 mg/kg/day for more than 3 months), and at least two of the following: azathioprine, mycophenolate mofetil, gold, tetracycline (or minocycline), cyclosporin, methotrexate, gold, or plasmapheresis. Failure is defined as the inability to wean steroids to less than 0.5 mg/kg/day. Potential candidates must have involvement of more than 10% of skin body surface area, involvement of one or more mucosal lesions, or recurrent infections requiring more than two hospitalizations in which the source of the infection was due to bullous skin disease. All candidates must be evaluated by two dermatologists, Dr. Joan Guitart and Dr. Joaquin Brieva, who must concur that the patient has refractory disease that may, in their clinical judgement, be associated with a 5-10% mortality if not controlled. A minimum of 2.0 x 106 CD34+ cells/kg after selection are necessary to proceed to transplant. Exclusion Criteria: Individuals less than 18 years of age. Significant end organ damage such as: LVEF <40% or deterioration of LVEF during exercise test on MUGA or echocardiogram. Untreated life-threatening arrhythmia. Active ischemic heart disease or heart failure. DLCO <45% or FEV1/FEV < 50%. Serum creatinine > 2.5 mg/dl. Liver cirrhosis, transaminases >3x of normal limits or bilirubin >2.0 unless due to Gilberts disease. HIV positive. Uncontrolled diabetes mellitus, or any other illness that in the opinion of the investigators would jeopardize the ability of the patient to tolerate aggressive treatment. Prior history of malignancy except localized basal cell or squamous skin cancer. Other malignancies for which the patient is judged to be cured by local surgical therapy, such as (but not limited to) head and neck cancer, or stage I or II breast cancer will be considered on an individual basis. Positive pregnancy test, inability or unable to pursue effective means of birth control, or failure to willingly accept or comprehend irreversible sterility as a side effect of therapy. Psychiatric illness or mental deficiency making compliance with treatment or informed consent impossible. Inability to give informed consent. Major hematological abnormalities such as platelet count less than 100,000/ul, or ANC less than 1000/ul. Presence of infected skin lesions. All skin lesions should be free of suppurative exudate.

Sites / Locations

  • Northwestern University, Feinberg School of Medicine

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

stem cell transplantation

Arm Description

Outcomes

Primary Outcome Measures

Percent surface area involved New skin or mucosal blister development Immune suppressive medication requirements Survival

Secondary Outcome Measures

Full Information

First Posted
January 16, 2006
Last Updated
April 4, 2013
Sponsor
Richard Burt, MD
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1. Study Identification

Unique Protocol Identification Number
NCT00278642
Brief Title
Hematopoietic Stem Cell Support in Patients With Autoimmune Bullous Skin Disorders
Official Title
High Dose Cyclophosphamide & ATG With Hematopoietic Stem Cell Support in Patients With Autoimmune Bullous Skin Disorders: A Phase I Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2013
Overall Recruitment Status
Terminated
Why Stopped
sponsor stopped the study because of lack of elligible participants
Study Start Date
September 2002 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
September 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Richard Burt, MD

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Autoimmune Bullous Skin Disorders are believed to be due to immune cells, cells that normally protect the body and are now causing damage to the body. This study is designed to examine whether treating patients with high dose cyclophosphamide (a drug which reduces the function of the immune system) together with anti-thymocyte globulin (a protein that kills the immune cells that are thought to be causing your disease), followed by return of the previously collected special blood cells (stem cells) will result in improvement of this disease. 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 intense chemotherapy is to destroy the cells in the immune system which may be causing this skin disease. The purpose of the stem cell infusion is to restore the body's blood production, which will be severely impaired by the high dose chemotherapy and anti-thymocyte globulin.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pemphigus

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
1 (Actual)

8. Arms, Groups, and Interventions

Arm Title
stem cell transplantation
Arm Type
Experimental
Intervention Type
Biological
Intervention Name(s)
Hematopoietic stem cell transplantation
Intervention Description
Autologous hematopoietic stem cell transplantation
Primary Outcome Measure Information:
Title
Percent surface area involved New skin or mucosal blister development Immune suppressive medication requirements Survival
Time Frame
5 years after transplant

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Less than chronologic age 60 years at the time of pre-transplant evaluation. An established diagnosis of an autoimmune skin disorder that includes any of the following: pemphigus vulgaris pemphigus foliaceus Diagnosis of bullous skin lesions will be based on history and physical, skin biopsy (light microscopy and indirect fluorescence), indirect immunofluorescence titer, BP 180 and 230 titers, Desmolglein-3 and Desmoglein-1 antibody, and photograph. Patients who failed corticosteroids (equivalent dosage of prednisone 0.5 mg/kg/day for more than 3 months), and at least two of the following: azathioprine, mycophenolate mofetil, gold, tetracycline (or minocycline), cyclosporin, methotrexate, gold, or plasmapheresis. Failure is defined as the inability to wean steroids to less than 0.5 mg/kg/day. Potential candidates must have involvement of more than 10% of skin body surface area, involvement of one or more mucosal lesions, or recurrent infections requiring more than two hospitalizations in which the source of the infection was due to bullous skin disease. All candidates must be evaluated by two dermatologists, Dr. Joan Guitart and Dr. Joaquin Brieva, who must concur that the patient has refractory disease that may, in their clinical judgement, be associated with a 5-10% mortality if not controlled. A minimum of 2.0 x 106 CD34+ cells/kg after selection are necessary to proceed to transplant. Exclusion Criteria: Individuals less than 18 years of age. Significant end organ damage such as: LVEF <40% or deterioration of LVEF during exercise test on MUGA or echocardiogram. Untreated life-threatening arrhythmia. Active ischemic heart disease or heart failure. DLCO <45% or FEV1/FEV < 50%. Serum creatinine > 2.5 mg/dl. Liver cirrhosis, transaminases >3x of normal limits or bilirubin >2.0 unless due to Gilberts disease. HIV positive. Uncontrolled diabetes mellitus, or any other illness that in the opinion of the investigators would jeopardize the ability of the patient to tolerate aggressive treatment. Prior history of malignancy except localized basal cell or squamous skin cancer. Other malignancies for which the patient is judged to be cured by local surgical therapy, such as (but not limited to) head and neck cancer, or stage I or II breast cancer will be considered on an individual basis. Positive pregnancy test, inability or unable to pursue effective means of birth control, or failure to willingly accept or comprehend irreversible sterility as a side effect of therapy. Psychiatric illness or mental deficiency making compliance with treatment or informed consent impossible. Inability to give informed consent. Major hematological abnormalities such as platelet count less than 100,000/ul, or ANC less than 1000/ul. Presence of infected skin lesions. All skin lesions should be free of suppurative exudate.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard Burt, MD
Organizational Affiliation
Northwestern University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern University, Feinberg School of Medicine
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States

12. IPD Sharing Statement

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Hematopoietic Stem Cell Support in Patients With Autoimmune Bullous Skin Disorders

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