Donor-Derived Cell-Free DNA Stratifies Risk of Mortality and Graft Dysfunction in Severe Acute Cardiac Allograft Rejection
Safiullah, Z.; Su, H.; Kong, H.; Jang, M. K.; Shah, K.; Berry, G. J.; Shah, P.; Valantine, H. A.; Tian, X.; Agbor-Enoh, S.
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BackgroundCardiac acute rejection (AR) is a risk factor for poor outcomes, however there are limited risk prediction models to stratify patients for death or sustained LV dysfunction. This study assesses the prognostic utility of percentage donor-derived cell-free DNA (%dd-cfDNA) at the diagnosis of AR for poor outcomes. MethodsThe prospective multicenter GRAfT study enrolled heart transplant recipients and collected serial plasma samples to quantitate %dd-cfDNA. AR was defined as acute cellular rejection (ACR), antibody-mediated rejection (AMR), as well as biopsy-negative AMR (donor-specific antibody positivity with LV dysfunction). AR was classified as mild-to-moderate (ACR grade 2 or AMR grade 1) or severe (ACR grade [≥]3, AMR grade [≥]2, or DSA+/LV dysfunction) and further stratified by a %dd-cfDNA threshold of 0.25%. Regression models assessed the association between AR and %dd-cfDNA levels at the AR diagnosis with the primary composite outcome of sustained LVEF decline <50% and/or death. ResultsThe study included 275 patients and 3,190 %dd-cfDNA assessments. Over the median of 4.6 (IQR 1.8 - 5.0) years follow-up, 51 patients experienced the composite outcome of death or prolonged EF reduction, and 75 patients developed AR, including 16.2% patients with ACR, 9.4% with pathologic AMR, and 6.6% with DSA+/LV dysfunction. Thirty-two (42.7%) patients had severe AR and 43 (57.3%) had mild-to-moderate AR. Severe--but not mild-to-moderate-- AR was associated with an increased risk of the primary composite endpoint (HR = 5.17, 95% CI 2.38 - 11.3, p < 0.001). Among those with severe AR, a %dd-cfDNA level greater than 0.25% at diagnosis was associated with a higher risk of the primary outcome (HR, 6.06, 95% CI, 1.78- 20.6; p = 0.004). Percent dd-cfDNA remained elevated in severe AR patients with adverse outcomes. ConclusionSevere AR with high %dd-cfDNA levels is associated with an increased risk of poor outcomes, offering novel prognostic utility. Clinical PerspectiveO_ST_ABSWhat is New?C_ST_ABSO_LIPercent donor-derived cell-free DNA (%dd-cfDNA) can risk stratify cardiac transplant patients with severe acute rejection for death and/or prolonged EF reduction C_LIO_LIPercent dd-cfDNA remain persistently elevated in patients with severe acute rejection who develop poor outcomes, which could reflect ineffective treatment. C_LIO_LIIn the contemporary era of cardiac transplantation, acute rejection defined by biopsy or by donor specific antibodies plus LV dysfunction is associated with poor outcomes C_LI What are the Clinical Implications?O_LIPercent dd-cfDNA could serve as a bedside tool to risk stratify patients with severe acute rejection for poor outcomes. C_LIO_LITrends of %dd-cfDNA could serve to monitor response to treatment for severe acute rejection. C_LIO_LIPercent dd-cfDNA levels at diagnosis of rejection could be leveraged for patient selection in clinical trials to test novel therapies or treatment strategies. C_LI
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