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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00587574
Other study ID # 488/2007
Secondary ID EK Nr 488/2007
Status Recruiting
Phase N/A
First received December 21, 2007
Last updated January 4, 2008
Start date October 2007
Est. completion date December 2011

Study information

Verified date October 2007
Source Medical University of Vienna
Contact Hildegard T Greinix, Professor
Phone +43140400
Email hildegard.greinix@meduniwien.ac.at
Is FDA regulated No
Health authority Austria: Ethikkommission
Study type Observational

Clinical Trial Summary

Allogeneic hematopoietic cell transplantation offers high cure rates for patients with hematological and oncological diseases. Graft-versus-host disease (attack of donor's white blood cells on patient's tissues) is a serious complication also affecting the patient's immune system. Therefore, patients in the early phase after allogeneic cell transplantation are at high risk for severe infectious complications. So far, no predictive biomarkers for the development of the chronic form of graft-versus-host disease are available. By analysing serially immune cell populations of the peripheral blood we will investigate whether certain subsets of cells are associated with development of chronic graft-versus-host disease. In addition, the patients' immune regeneration will be evaluated by serial analyses of peripheral blood immune cell populations 3 months to 2 years after allogeneic cell transplantation.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date December 2011
Est. primary completion date December 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Receiving grafts from either HLA-identical sibling donors or HLA-matched unrelated donors

- Receiving grafts from HLA-mismatched sibling donors or HLA-mismatched unrelated donors

- Receiving either bone marrow, peripheral blood stem cells or cord blood grafts

- Alive on day 100 after transplant

- Age 18 years or above

- Signed written informed consent

Exclusion Criteria:

- Lymphocytopenia not allowing immunophenotyping

- Treatment with rituximab after HSCT until study entry

- Hepatitis B and C, HIV infection

- Secondary posttransplant malignancies including EBV-lymphoproliferative disease

- Karnofsky score of 30 or below

- Absence of informed consent

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Austria Medical University of Vienna Vienna
Czech Republic Institute of Hematology and Blood Transfusions Prague Prague

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Countries where clinical trial is conducted

Austria,  Czech Republic, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation of perturbed B cell homeostasis with chronic graft-versus-host disease activity of immune system October 2007 until December 2010 No
Secondary Difference of time-dependent pattern of immune reconstitution after allogeneic cell transplantation between patients with and without chronic graft-versus-host disease October 2010 until December 2010 No
Secondary Compare number of clinically defined bacterial, viral and fungal infectious episodes between patients with and without chronic graft-versus-host disease October 2007 until December 2010 No
Secondary Compare the number of circulating T, DC, NK subsets in patients with and without chronic GVHD to identify their respective role in development and prolongation of chronic GVHD October 2007 until December 2010 No
Secondary Investigate the impact of different immunosuppressive/immunomodulatory treatments for chronic GVHD on various immune cell populations October 2007 until December 2010 No
Secondary Assess the chimerism of antigen-presenting cells in circulation and tissue specimens and correlate it with occurrence of chronic GVHD October 2007 until December 2010 No