Hepatitis C and liver transplantation

Silvia Martini1

  • 1Unit of Gastrohepatology, AOU Città della Salute e della Scienza di Torino, Turin, Italy - smartini@cittadellasalute.to.it.

Insights

Direct-acting antiviral agents (DAAs) offer curative treatment for Hepatitis C virus (HCV) infection, impacting liver transplantation (LT) decisions. Optimal timing for DAA treatment in LT candidates and recipients remains under investigation.

Area of Science:

  • Hepatology and Transplant Surgery
  • Virology and Infectious Diseases
  • Pharmacology and Therapeutics

Background:

  • Hepatitis C virus (HCV) infection is a primary driver for liver transplantation (LT) in the USA and Europe.
  • HCV recurrence post-LT is nearly universal in viremic recipients.
  • Previous treatments like pegylated-interferon and ribavirin had limited efficacy and applicability.

Purpose of the Study:

  • To review the impact of direct-acting antiviral agents (DAAs) on HCV management in liver transplantation.
  • To discuss optimal timing for DAA treatment initiation in relation to LT (pre-LT, early post-LT, or post-recurrence).
  • To explore the potential of using HCV-positive donors to expand the donor pool.

Main Methods:

  • Review of published data on DAA efficacy and safety in liver transplant recipients and candidates.
  • Analysis of trends in LT wait-listing for HCV-related liver disease.
  • Discussion of clinical considerations for DAA treatment strategies.

Main Results:

  • DAAs have significantly improved curative treatment options for HCV in the transplant population.
  • The use of HCV-positive donors is a potential strategy to increase donor availability.
  • LT wait-listing for HCV with decompensated cirrhosis decreased by 32% in the US during 2014-2015 DAA era.

Conclusions:

  • DAA treatment is highly applicable to patients with decompensated cirrhosis and liver transplant recipients.
  • The advent of DAAs is shifting the landscape of HCV management, potentially reducing LT rates.
  • Further research is needed to determine the optimal timing for DAA therapy in the LT pathway.