Efficacy and Safety Study of Allogenic Mesenchymal Stem Cells for Patients With Chronic Graft Versus Host Disease (MSCsTcGVHD)
Primary Purpose
Chronic Graft Versus Host Disease
Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Biological: mesenchymal stem cell
Cyclosporine and Glucocorticoid
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Graft Versus Host Disease focused on measuring cGVHD
Eligibility Criteria
Inclusion Criteria:
- Extensive cGVHD with skin and/or liver damage developed after allogeneic hematopoietic stem cell transplantation
- cGVHD that do not response to conventional immunosuppressant treatment for two months
- KPS>= 30
- informed consent from the patient
Exclusion Criteria:
- Extensive cGVHD without skin or liver damage
- With other acute severe complications
- In pregnancy or lactation
- Disease relapses
- With non-hematological malignancy
- Have a history of mental disorder, drug or alcohol abuse over the past five years
- Allergic
- Participate in other clinical trial within three months before the start of this trial
- With bone marrow fibrosis
- Have undergone hematopoietic stem cell transplantation to treat solid tumor
Sites / Locations
- Zhejiang UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
allogenic mesenchymal stem cells (MSCs)
Control group
Arm Description
patients who have developed an extensive chronic graft versus host disease (with skin and/or liver damage) after HSCs transplantation and do not respond to standard first-line regimen including cyclophosphamide and prednisolone.
patients who have developed an extensive chronic graft versus host disease (with skin and/or liver damage) after HSCs transplantation and do not respond to standard first-line regimen including cyclophosphamide and prednisolone.
Outcomes
Primary Outcome Measures
The total Response rate defined as patients with complete and partial response
Secondary Outcome Measures
one-year survival rate
disease relapse
quality of life
Full Information
NCT ID
NCT01526850
First Posted
February 1, 2012
Last Updated
August 1, 2012
Sponsor
Chinese Academy of Medical Sciences
Collaborators
Zhejiang University, Chinese PLA General Hospital, 307 Hospital of PLA, Peking Union Medical College
1. Study Identification
Unique Protocol Identification Number
NCT01526850
Brief Title
Efficacy and Safety Study of Allogenic Mesenchymal Stem Cells for Patients With Chronic Graft Versus Host Disease
Acronym
MSCsTcGVHD
Official Title
Phase Ⅱ/Ⅲ Clinical Trial, Multicenter, Randomized, Controlled, for the Evaluation of Efficacy and Safety of Therapy With Allogenic Mesenchymal Stem Cells in Patients With Chronic Graft Versus Host Disease
Study Type
Interventional
2. Study Status
Record Verification Date
February 2012
Overall Recruitment Status
Unknown status
Study Start Date
February 2012 (undefined)
Primary Completion Date
December 2013 (Anticipated)
Study Completion Date
June 2014 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese Academy of Medical Sciences
Collaborators
Zhejiang University, Chinese PLA General Hospital, 307 Hospital of PLA, Peking Union Medical College
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The primary purpose of the study is to evaluate the safety and efficacy of mesenchymal stem cells (MSC) for the treatment of patients who have developed an extensive chronic graft versus host disease (with skin and/or liver damage) after HSCs transplantation and do not respond to first-line therapy.
The secondary purpose of the study is to evaluate the effect of mesenchymal stem cells (MSC) on one-year survival rate, long-term survival rate, life quality and recurrence of patients who have developed an extensive chronic graft versus host disease (with skin and/or liver damage) after HSCs transplantation and do not respond to hormone treatment.
Detailed Description
Chronic Graft-versus-host disease (GVHD), with the incidence of 30%-60%, is a serious late complication of allogeneic hematopoietic stem cell transplantation (HSCT) and is the major cause of death in the late stage of transplantation. According to targeted organs, cGVHD is divided into two types, limited cGVHD and extensive cGVHD. Extensive cGVHD needs systemic immunosuppressant treatment. However, currently standard first-line regimen including cyclophosphamide and prednisolone is only effective for some patients. Novel treatment is urgently needed. Our previous study has shown that mesenchymal stem cells (MSCs) are effective for cGVHD patients with multiple skin damage. To further explore the therapeutic effect of MSCs for extensive cGVHD, we plan to conduct a multi-center clinical trial. Patients who developed an extensive cGVHD (with skin and/or liver damage) after HSCs transplantation and do not respond to first-line therapy are enrolled. They will be randomly divided into two groups which will receive MSCs and routine second-line drugs respectively. We will evaluate the efficacy and safety of MSCs for extensive cGVHD by comparison of symptom improvement, survival rate, recurrence as well as side effects in the two groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Graft Versus Host Disease
Keywords
cGVHD
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
allogenic mesenchymal stem cells (MSCs)
Arm Type
Experimental
Arm Description
patients who have developed an extensive chronic graft versus host disease (with skin and/or liver damage) after HSCs transplantation and do not respond to standard first-line regimen including cyclophosphamide and prednisolone.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
patients who have developed an extensive chronic graft versus host disease (with skin and/or liver damage) after HSCs transplantation and do not respond to standard first-line regimen including cyclophosphamide and prednisolone.
Intervention Type
Biological
Intervention Name(s)
Biological: mesenchymal stem cell
Other Intervention Name(s)
Regenerative medicine: MSCs
Intervention Description
Mesenchymal stem cells, 1-2×107, bone marrow injection, once a week for the first four weeks; whether to continue after four weeks depends on patients' symptoms.
Intervention Type
Drug
Intervention Name(s)
Cyclosporine and Glucocorticoid
Other Intervention Name(s)
Calmodulin inhibitors combined with Glucocorticoid
Intervention Description
Calmodulin inhibitors such as cyclosporine, combined with Glucocorticoid 0.5-1mg/kg/d ,to the end of the study.
Primary Outcome Measure Information:
Title
The total Response rate defined as patients with complete and partial response
Time Frame
1 year after MSCs administration.
Secondary Outcome Measure Information:
Title
one-year survival rate
Time Frame
1 year after MSCs administration
Title
disease relapse
Time Frame
2 years after MSCs administration
Title
quality of life
Time Frame
2 years after MSCs administration
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Extensive cGVHD with skin and/or liver damage developed after allogeneic hematopoietic stem cell transplantation
cGVHD that do not response to conventional immunosuppressant treatment for two months
KPS>= 30
informed consent from the patient
Exclusion Criteria:
Extensive cGVHD without skin or liver damage
With other acute severe complications
In pregnancy or lactation
Disease relapses
With non-hematological malignancy
Have a history of mental disorder, drug or alcohol abuse over the past five years
Allergic
Participate in other clinical trial within three months before the start of this trial
With bone marrow fibrosis
Have undergone hematopoietic stem cell transplantation to treat solid tumor
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
He Huang, MD
Phone
86-0571-87236706
Email
hehuangyu@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
He Huang, MD
Organizational Affiliation
Zhejiang University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Chunhua Zhao, MD,PHD
Organizational Affiliation
Peking Union Medical College
Official's Role
Principal Investigator
Facility Information:
Facility Name
Zhejiang University
City
Hangzhou
State/Province
Zhejiang
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
He Huang, MD
Phone
86-0571-87236706
Email
hehuangyu@126.com
12. IPD Sharing Statement
Citations:
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21235326
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Efficacy and Safety Study of Allogenic Mesenchymal Stem Cells for Patients With Chronic Graft Versus Host Disease
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