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◆ JACC Heart Failure2026-06-05· Medicine

Donor-Derived Cell-Free DNA as a Prognostic Biomarker After Heart Transplantation

Palak Shah, Paul J. Kim, Kelly H. Schlendorf, David A. Baran, Monica M. Colvin, Adam D. DeVore, Howard J. Eisen, Kambiz Ghafourian, Michael M. Givertz, Eileen Hsich, Jaime L.W. Kennedy, E V A N Kransdorf, José Nativi-Nicolau, Jignesh Patel, Eleni Tseliou, Omar Wever-Pinzon, Andrew Doud, Michelle S. Bloom, Sandra Carey, Navchetan Kaur, D. Giovanni Biagini, Kyle E. Marshall, Michael Olympios, Mandeep R. Mehra, J Stehlik

原始摘要(英文原文)· Original abstract
BACKGROUND: Measurement of donor-derived cell-free DNA fraction (dd-cfDNA%) and donor quantity score (DQS) is a noninvasive biomarker of acute rejection in heart transplantation (HT). Its prognostic value beyond histopathology remains uncertain. OBJECTIVES: This study sought to evaluate associations between donor-derived cell-free DNA (dd-cfDNA) and clinically meaningful outcomes using a composite endpoint of treated rejection, graft dysfunction, retransplantation, or death within 1 year post-HT. METHODS: The DEFINE-HT (Development of Noninvasive Cell-free DNA to Supplant Invasive Biopsy in Heart Transplantation) was a prospective, observational study following adult HT recipients at 10 U.S. centers for 1-year post-HT; blood was collected for dd-cfDNA testing (Prospera Heart) during surveillance and for-cause evaluations, independent of clinical decision-making. Treated rejection included biopsy-positive or biopsy-negative rejection requiring augmented immunomodulation. Graft dysfunction was defined as >10% decline in left ventricular ejection fraction from baseline to <50%. Time-varying Andersen-Gill models assessed associations between dd-cfDNA and events. RESULTS: Among 110 patients (median age 55 years, 25.5% female, 22% Black), 38 (34.5%) met the primary composite endpoint: treated rejection (20%), graft dysfunction (10.9%), death (3.6%), and retransplantation (0%). Furthermore, 4.6% of endomyocardial biopsies demonstrated rejection and 90% of dd-cfDNA results were below threshold. dd-cfDNA% and DQS were higher in treated vs untreated biopsy-positive rejection (0.23% vs 0.085%; P = 0.045, and 27 vs 9 copies/mL; P = 0.012, respectively). No patients with graft dysfunction had biopsy-positive rejection despite elevated dd-cfDNA. One-intrapatient-SD increases in dd-cfDNA% and DQS were associated with 19% and 12% higher risk of the primary endpoint (P < 0.001). Above-threshold dd-cfDNA levels also conferred 4.42-fold increased risk of the composite endpoint (P < 0.001). CONCLUSIONS: DEFINE-HT supports the potential role of dd-cfDNA as a prognostic biomarker of graft health and informs a randomized trial comparing dd-cfDNA and biopsy-based monitoring. (Development of Noninvasive Cell-free DNA to Supplant Invasive Biopsy in Heart Transplantation [DEFINE-HT]; NCT05309382).
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