Single Center Experience Comparing Two Clinically Available Donor Derived Cell Free DNA Tests
1UCLA, Los Angeles, CA, 2Pharmacy, David Geffen School of Medicine at UCLA, Los Angeles, CA, 3David Geffen School of Medicine at UCLA, Los Angeles, CA
Meeting: 2021 American Transplant Congress
Abstract number: 631
Keywords: Kidney transplantation, Monitoring, Rejection
Topic: Clinical Science » Biomarkers, Immune Assessment and Clinical Outcomes
Session Information
Session Name: Biomarkers, Immune Assessment and Clinical Outcomes
Session Type: Poster Abstract
Session Date & Time: None. Available on demand.
Location: Virtual
*Purpose: Donor derived cell-free DNA (dd cf-DNA), this new technology allows for non-invasive monitoring of graft function. Two most commonly used assays are Prospera (Natera®, San Carlos, California) and AlloSure (CareDx®, Brisbane, California). We report our experience in comparing simultaneous use of these tests.
*Methods: A series of 15 paired-samples from individual kidney transplant recipients using Prospera and AlloSure test were included. We used the company cut off of >1% to indicate active rejection for Prospera, and 0.5% or 1% for Allosure. Acute rejections were all defined by kidney histology.
*Results: The paired-results are shown in Table 1. There were concordant results for all 15 paired-samples when using Allosure cut off level of 0.5%. A single discordant result was observed when using Allosure cut off level of 1%. Kidney biopsies were performed in seven of the cases where dd cf-DNA was elevated. Rejection was found in six of biopsy results (see in table 2). When cut off level of 1% was used, Prospera identified 80% (4/5) of T-cell mediated rejections (TCMR) compared to 60% for Allosure (3/5). Both assays recognized the single case of antibody mediated rejection. When using cut off level of 0.5% for Allosure, all 6/6 rejections were identified.
*Conclusions: There were concordant results between the two using cut off of 1% for Prospera and 0.5% for Allosure. The accuracy of the result was confirmed by the kidney biopsy (5 active rejection diagnosis + 1 non-rejection). Prospective, head-to-head trials are needed to compare the accuracy and predictive values of these two clinically available dd-cfDNA assays.
To cite this abstract in AMA style:
Bunnapradist S, Lee S, Homkrailas P, Danovitch G. Single Center Experience Comparing Two Clinically Available Donor Derived Cell Free DNA Tests [abstract]. Am J Transplant. 2021; 21 (suppl 3). https://atcmeetingabstracts.com/abstract/single-center-experience-comparing-two-clinically-available-donor-derived-cell-free-dna-tests/. Accessed November 21, 2024.« Back to 2021 American Transplant Congress