Study Correlation Between Blood, Tissue Gene Expression, Donor Derived Cell Free DNA and Histopathology in Kidney Transplant Recipients

Sponsor
Rush University Medical Center (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05811468
Collaborator
(none)
30
24

Study Details

Study Description

Brief Summary

This study will compare the performance of Gene Expression Profile (GEP)/ Donor derived cell free deoxyribonucleic acid (dd-cfDNA) tests, to the following tests: Molecular Microscope (MMDx) and histopathology (study of changes in tissues caused by disease) in their ability to diagnose (exactly identify) various types of injury within the transplanted kidney.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This study will evaluate the performance of the blood-based assays like gene expression panel (GEP), and donor derived cell free DNA (dd-cfDNA) against tissue-based assays like molecular microscope (MMDX) and histopathology in their ability to more accurately detect presence of rejection among kidney transplant recipients deemed at higher than usual risk for immunologic injury i.e., rejection.

    Furthermore, the study should shed light on the ability of the different blood- based assays to accurately discern between the different types of rejection (early cellular versus humoral) against such confirmed by histopathology and molecular microscope.

    The study will also shed light on the ability of these noninvasive biomarkers to be utilized as a tool of immunomodulation in addition to studying their ability to accurately confirm presence of adequately treated rejection among the recipients of kidney transplant.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    30 participants
    Observational Model:
    Case-Only
    Time Perspective:
    Prospective
    Official Title:
    Pilot Study to Evaluate the Correlation Between Peripheral Gene Expression Profile Testing, Tissue-based Gene Expression Profiling, Donor Derived Cell Free DNA, and Histopathology Among High-risk Kidney Transplant Recipients
    Anticipated Study Start Date :
    May 30, 2023
    Anticipated Primary Completion Date :
    May 30, 2024
    Anticipated Study Completion Date :
    May 30, 2025

    Outcome Measures

    Primary Outcome Measures

    1. Quantify the number of rejections in the kidney allograft detected via non invasive blood- based testing as reflected in abnormal laboratory readout of GEP value and dd-CFDNA fraction. [Through study completion, an average of 1 year]

      The number of rejections in the kidney allograft detected via blood- based non invasive testing will be measured and compared to the number of rejection cases detected by histopathology and MMDX to ascertain accuracy of blood based assays to detect rejection among kidney transplant recipients

    2. Quantify the number of rejection cases detected by histopathology and MMDX as reported by respective pathology laboratories/ pathologists [Through study completion, an average of 1 year]

      Measure the number of rejections in the kidney allograft detected by histopathology and MMDX as invasive tests and ascertain concordance of those results with blood based non invasive assays.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 100 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    • Patients undergoing a for cause biopsy due to ongoing or suspected "injury" of the allograft.

    • Patients will be between 3 months and 7 years post-transplant episode.

    • Recipients of both cadaveric and living donor renal transplant are considered eligible.

    Exclusion Criteria:
    • No multi organ transplant recipients will be included.

    • Pregnancy

    • HIV positive recipients

    • Recipients of kidney transplant from an identical sibling

    • Patients with active and biopsy proven BK nephropathy

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Rush University Medical Center

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Vasil Peev, Physician, Rush University Medical Center
    ClinicalTrials.gov Identifier:
    NCT05811468
    Other Study ID Numbers:
    • 22060707
    First Posted:
    Apr 13, 2023
    Last Update Posted:
    Apr 13, 2023
    Last Verified:
    Apr 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Vasil Peev, Physician, Rush University Medical Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 13, 2023