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Mesenchymal Stem Cells as a Treatment for Oral Complications of Graft-versus-host Disease

Primary Purpose

Graft -Versus-host-disease

Status
Withdrawn
Phase
Phase 1
Locations
Sweden
Study Type
Interventional
Intervention
Mesenchymal stromal cells
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Graft -Versus-host-disease focused on measuring Graft-versus-host-disease, Immune system diseases, Oral

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Chronic graft-versus-host disease and oral manifestations grade 3 exhibiting severe symptoms, according to the NIH Consensus Working Group for Diagnosis and Staging of cGVHD and have failed frontline therapy

Exclusion Criteria:

  • Active malignancy
  • Fulfilling criteria for previously initiated study for treatment of chronic graft-versus-host disease

Sites / Locations

  • Oral and Maxillofacial Surgery, Karolinska Univeristy Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Mesenchymal stromal cell treatment

Arm Description

Biological: Mesenchymal stromal cells

Outcomes

Primary Outcome Measures

Change in disease activity according to National Institutes of Health criteria for oral graft-versus-host disease

Secondary Outcome Measures

Change in self-assessed disease activity and quality of life
Safety
Frequency of complications, infections and relapse

Full Information

First Posted
February 4, 2014
Last Updated
August 12, 2019
Sponsor
Karolinska Institutet
Collaborators
Region Stockholm
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1. Study Identification

Unique Protocol Identification Number
NCT02055625
Brief Title
Mesenchymal Stem Cells as a Treatment for Oral Complications of Graft-versus-host Disease
Official Title
Treatment of Oral Mucosa in Patients With Graft-versus-host Disease Following Injection of Mesenchymal Stem Cells - Human Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Withdrawn
Study Start Date
January 2014 (undefined)
Primary Completion Date
August 2019 (Actual)
Study Completion Date
August 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Region Stockholm

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Graft-versus-host disease (GVHD) is a major complication of allogeneic hematopoietic stem cell transplantation (HSCT), and is classified as acute (aGVHD) or chronic (cGVHD). aGVHD onsets within the first 100 days after transplant or with clinical features including erythema, liver dysfunction and oral mucositis, whilst cGVHD or persistent GVHD occurs in approximately 30-60% of transplant patients who survive their first year . Long-term five-year prognosis for cGVHD patients is poor with a 70% mortality rate. cGVHD manifests as an autoimmune-like disease affecting multiple sites, including skin, mouth, eyes, gastrointestinal tract, liver, and joints. The oral cavity is the second most common site to be affected with symptoms in 45-83% of cases. In the mouth a diverse spectrum of clinical features can be found for example mucosal lesions can affect almost any site, salivary gland dysfunction and restricted mouth opening. Short-term patients can experience mucosal sensitivity, malnutrition, problems speaking, increased caries risk, xerostomia, oral pain and a diminished quality-of-life. Long-term complications include secondary malignancies and perhaps early death. Clinical management seeks to alleviate the symptoms and improve quality-of-life but 50% of patients fail front-line systemic steroid therapy. Oral cGVHD can be treated with topical high potency corticosteroids and oral rinses, however these treatments are not always effective and carry a risk of systemic absorption. Mesenchymal stem/stromal cells (MSCs) resident in adult and fetal tissues, such as the bone marrow have the capacity to form bone, cartilage, stroma, muscle and fat, are known to exhibit immunosuppressive and immunoregulatory properties both in vivo and in vitro. MSC infusions have been used to treat disorders such as osteogenic imperfecta, cardiovascular disease and to heal large bony defects. Indeed, the immunosuppressive capacity of MSCs have led to infusions being used as a second-line treatment for GVHD patients, and our group has shown within a Phase II clinical trial, 55% aGVHD patients who failed front-line steroid treatment responded to MSC infusion these studies are going with cGVHD patients. The goal of this project is to perform a pilot study to determine whether MSC injections directly into mucosal lesions in patients with oral cGVHD are able to alleviate the symptoms and facilitate the reparative process.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Graft -Versus-host-disease
Keywords
Graft-versus-host-disease, Immune system diseases, Oral

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mesenchymal stromal cell treatment
Arm Type
Experimental
Arm Description
Biological: Mesenchymal stromal cells
Intervention Type
Biological
Intervention Name(s)
Mesenchymal stromal cells
Intervention Description
Allogenous mesenchymal stromal cells will be injected directly underneath the mucosal lesions at one side under local anesthetic at 2.5-4 million cells/ml. A total of approximately 1.7 ml will be injected divided in 2-3 injections around the lesion. Patients will be followed every second day up to 7 days afterwards and then routinely at 14 days, 1 month, 2 months and 6 months to assess the healing process.
Primary Outcome Measure Information:
Title
Change in disease activity according to National Institutes of Health criteria for oral graft-versus-host disease
Time Frame
Baseline to 6 months
Secondary Outcome Measure Information:
Title
Change in self-assessed disease activity and quality of life
Time Frame
Baseline to 6 months
Title
Safety
Description
Frequency of complications, infections and relapse
Time Frame
Baseline to 21 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Chronic graft-versus-host disease and oral manifestations grade 3 exhibiting severe symptoms, according to the NIH Consensus Working Group for Diagnosis and Staging of cGVHD and have failed frontline therapy Exclusion Criteria: Active malignancy Fulfilling criteria for previously initiated study for treatment of chronic graft-versus-host disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Katarina Le Blanc, Professor
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Karin Garming-Legert, DDS, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rachael Sugars, BSc, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oral and Maxillofacial Surgery, Karolinska Univeristy Hospital
City
Stockholm
State/Province
Huddinge
ZIP/Postal Code
14186
Country
Sweden

12. IPD Sharing Statement

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Mesenchymal Stem Cells as a Treatment for Oral Complications of Graft-versus-host Disease

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