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HCV+ Organs Offer Better Waitlist, Survival Outcomes for Transplantation

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Direct-acting antiviral agents have enabled more availability for organ transplant.

New research has found that people waitlisted to receive hepatitis C virus (HCV)+ organs for transplant have better survival outcomes compared to people not listed to receive these organs, who are at a disadvantage in waitlist outcomes.1

“There remains a substantial supply-demand mismatch in liver transplantation with a growing need for organ availability. Efforts to expand the donor pool to combat this issue have prompted consideration of extended criteria donors. Initially, HCV + donor livers were either discarded or primarily used for transplantation in HCV nucleic acid amplification test (NAT)+ recipients due to concerns for transmission and graft loss. Since the development of direct-acting antiviral agents (DAA), utilization of HCV NAT+ organs has expanded for HCV NAT- recipients,” lead investigator Natalia Salinas Parra, MD, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, and colleagues wrote.1 “DAA therapies have optimal tolerability, safety, and efficacy when compared to prior interferon-based therapies to treat HCV. With the resulting decline in chronic HCV-related liver transplants and the broadening of the donor pool, DAA have changed the landscape of liver transplantation.”

Parra and colleagues evaluated trends in HCV NAT+ listing and impact on transplant probability, waitlist mortality, and likelihood of receiving HCV NAT+ organs in adult patients in the United Network for Organ Sharing dataset waitlisted for liver transplantation from 2016 to 2023.

The analysis included 21,776 patients initially listed for HCV NAT+ organs and 45,378 not. During this time, the proportion of waitlisted patients listed for these organs increased significantly from 8.8% to 60.8%, (P <.001). In 2021 to 2023, HCV NAT+ listing was associated with a waitlist mortality benefit (SHR 0.73 [95% CI, 0.68-0.79]; P <.001) and a 17% reduced hazard of overall mortality (HR 0.83 [95% CI, 0.78-0.89]; P <.001). A portion of the total protective effect on overall survival (16.0%) was associated with actual receipt of HCV NAT+ organs (TERERI of -0.160 and a PIE of -0.026; P <.001). Patients not listed for HCV NAT+ organs face a relative disadvantage in terms of waitlist outcomes.1

“In conclusion, while HCV NAT+ listings have risen substantially over time, there remains center-level and geographic variation in this practice, in addition to marginalized groups who are less likely to be listed for these organs. This is a critical issue to explore, as our analyses suggest that in the modern era of transplantation patients who do not agree to HCV NAT+ listing are relatively disadvantaged in terms of transplantation probability and waitlist mortality reduction. Future research should explore patient and provider/factors that contribute to low rates of HCV NAT+ listing as this may elucidate targeted interventions to promote equity in transplant,” Parra and colleagues concluded.1

Other recent research into liver transplantation found that a direct alcohol biomarker, phosphatidylethanol (PEth), could positively impact the surveillance of alcohol use after liver transplantation in patients with alcohol-related liver disease (ALD). An analysis found that PEth use could provide rapid and early detection of alcohol use among those transplanted for ALD— a population of 46 patients with ≥1 alcohol relapse episode revealed approximately 76% detected by PEth alone.2

REFERENCES
  1. Parra NS, Hoteit MA, Rattan P, Abt P, Mahmud N. Trends in candidate HCV NAT+ listing and associated impacts on liver transplantation waitlist outcomes. Am. J. Transplant. Published online October 24, 2024. doi: 10.1016/j.ajt.2024.10.016
  2. De La Torre SA, Ibrahim B, Meneses K, Saab S, Shetty A. Impact of phosphatidylethanol in the surveillance for alcohol use in post-liver transplant population: A retrospective study. Alcohol Clin Exp Res (Hoboken). 2024 Oct 31. doi: 10.1111/acer.15474. Epub ahead of print. PMID: 39482857.

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