Ann Surg Treat Res.  2018 Sep;95(3):147-151. 10.4174/astr.2018.95.3.147.

Use of direct antiviral agents in liver transplant recipients with hepatitis C virus in Korea: 2-center experience

Affiliations
  • 1Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • 2Department of Surgery, Seoul National University College of Medicine, Seoul, Korea. kwleegs@gmail.com
  • 3Division of Gastroenterology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Abstract

PURPOSE
The proportion of liver recipients with HCV is gradually increasing in Korea. Limited data are available regarding the efficacy of direct antiviral agents (DAAs) in liver transplant recipients in Asia. We aimed to assess the efficacy and safety of DAAs in HCV-infected liver recipients in Korea.
METHODS
Forty HCV-infected patients from 2 centers received DAAs in the pretransplant or posttransplant period between May 2015 and November 2016.
RESULTS
DAA was administered in the pretransplant period in 6 patients and the posttransplant period in 34 patients. Dalastavir and asunaprevir (n = 2) and sofosbuvir/ledipasvir and ribvarin (n = 4) were used in the pretransplant period. HCV RNA was not detected before liver transplantation in all patients. Sustained virological response (SVR) at 12 and 24 weeks after liver transplantation was 100%. In the posttransplant period, 33 of 34 patients received sofosfovir-based therapy. SVR at 12 weeks in those patients was 94%. Recurrent virologic relapse developed in 2 patients because of HCC recurrence or treatment failure. Adverse events included anemia (n = 2) and abdominal discomfort (n = 1).
CONCLUSION
DAAs are an effective and well-tolerated treatment for HCV-infected recipients in Korea.

Keyword

Safety; Antiviral agents; Liver transplantation; Treatment outcome

MeSH Terms

Anemia
Antiviral Agents*
Asia
Hepacivirus*
Hepatitis C*
Hepatitis*
Humans
Korea*
Liver Transplantation
Liver*
Recurrence
RNA
Transplant Recipients*
Treatment Failure
Treatment Outcome
Antiviral Agents
RNA

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