Markers of Inflammation in Hematopoietic Stem Cell Transplant

NCT ID: NCT00579397

Last Updated: 2019-08-30

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 30 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2007-04-30
• Study Completion Date: 2012-12-12

Brief Summary

Objectives:

1. To show feasibility and reproducibility of performing a multiplex ligation-dependent amplification procedure (RT-MLPA)

2. To describe the profile of changes in inflammatory gene products, using RT-MLPA, in pediatric patients receiving stem cell transplant

3. To determine if changes in a specific inflammatory product, or a combination of inflammatory products, can predict grade 2-4 acute graft-versus-host disease

Detailed Description

Allogeneic Hematopoietic Stem Cell Transplantation (HSCT) is a successful treatment option for multiple malignant diseases (i.e. leukemia) and non-malignant disorders (i.e. metabolic disorders, genetic disorders, immunodeficiencies). Unfortunately, transplantation from an HLA-related family member is only available in 30-40% of stem cell transplant recipients. The other patients requiring HSCT must then receive their stem cells from either a matched-unrelated donor (MUD) or from cord blood. One major limitation upon receiving these unrelated stem cells are acute and chronic graft-versus-host disease. Specifically looking at acute graft-versus-host disease (aGVHD), up to 30% of the recipients of stem cells from an HLA-identical related donor will develop greater or equal to grade 2 of aGVHD despite immunosuppressive prophylaxis. The percentages of patients who develop aGVHD from unrelated donors are even higher.

The current standard treatment for aGVHD is corticosteroids. Unfortunately, only 40% of matched-siblings HSCT cases and 25% of MUD SCT cases show a complete response to these steroids. Those patients who do not respond to corticosteroids can show a dismal outcome. Given the poor outcome with refractory GVHD, there has been a lot of interest in trying to predict who will get GVHD. These findings could lead to augmentation of GVHD prophylaxis.

The purpose of this study is to look at a series of identified biomarkers to predict aGVHD. Once blood is drawn from the SCT recipient, a multiplex ligation-dependent probe amplification (MLPA) will test different biomarkers in the blood to result in about 30-45 target sequences being examined simultaneously.

Conditions

Acute Graft Versus Host Disease

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

1

For Objective #1:

• Healthy adult volunteers

No interventions assigned to this group

2

For Objectives #2 & #3:

• Recipients undergoing an allogeneic stem cell transplant

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Objective #1:
• Healthy adult volunteers, affiliated to Children's Memorial Hospital
• Male or female
• Objective #2 & #3:
• Recipient undergoing an allogeneic stem cell transplant
• Receiving related or unrelated cord blood, related or unrelated bone marrow or peripheral blood stem cells
• Any pre-transplant regimen
• Ages of 0-21 years old
• Male or female

Exclusion Criteria

• Inability for subject/parent to understand study and therefore unable to consent
• Children under 7.0 kgs

• Maximum Eligible Age: 21 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Ann & Robert H Lurie Children's Hospital of Chicago

OTHER

Sponsor Role: lead

Responsible Party

Reggie E Duerst, MD

Clinical Director - Stem Cell Transplant

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Reggie Duerst, MD

Role: PRINCIPAL_INVESTIGATOR

Ann & Robert H Lurie Children's Hospital of Chicago

Locations

Lurie Children's Hospital

Chicago, Illinois, United States

Countries

United States

Other Identifiers

SCT 0407

Identifier Type: -

Identifier Source: org_study_id