Risk of Hepatocellular Carcinoma After Spontaneous Clearance of Hepatitis C Virus and in Noncirrhosis Chronic Hepatitis C Patients With Sustained Virological Response: A Systematic Review

Author:

Hsu Christine C1,Gopalakrishna Harish1,Mironova Maria1,Lee Mei-Hsuan2,Chen Chien-Jen3,Yang Hwai-I3,Wiese Manfred4,Chang Kyong-Mi56,Wright Elizabeth C7,Abijo Tomilowo7,Feld Jordan J89,Kaplan David E56

Affiliation:

1. Liver Disease Branch, National Institute of Diabetes and Digestive and Kidney Diseases , Bethesda, Maryland , USA

2. Institute of Clinical Medicine, National Yang-Ming Chiao Tung University , Taipei , Taiwan

3. Genomics Research Center, Academia Sinica , Taipei , Taiwan

4. Department of Hepatology, University Hospital Leipzig, East German HCV Study Group , Leipzig , Germany

5. Division of Gastroenterology and Hepatology, University of Pennsylvania , Philadelphia, Pennsylvania , USA

6. Division of Gastroenterology and Hepatology, Corporal Michael J. Crescenz VA Medical Center , Philadelphia, Pennsylvania , USA

7. Office of the Director, National Institute of Diabetes and Digestive and Kidney Diseases , Bethesda, Maryland , USA

8. Department of Medicine, Division of Gastroenterology, Toronto Centre for Liver Disease, Toronto General Hospital, University Health Network , Toronto , Canada

9. Toronto Viral Hepatitis Care Network , Toronto , Canada

Abstract

AbstractIn a hepatitis C virus (HCV)–controlled human infection model (CHIM), healthy volunteers are inoculated with HCV and then treated. Residual hepatocellular carcinoma (HCC) risk after viral clearance is an important consideration when evaluating the CHIM. We estimate HCC risk in spontaneously cleared HCV and in noncirrhosis after sustained virological response (SVR) to HCV treatment in a systematic review and using data from 3 cohorts: German anti-D, Taiwan, and US Veterans Affairs (VA). For noncirrhosis SVR, the overall HCC rate is 0.33 per 100 patient-years in meta-analysis. HCC rates for the German, Taiwan, and US Veterans Affairs cohorts are 0, 0.14, and 0.02 per 100 patient-years, respectively. Past hepatitis B virus exposure was not accounted for in the Taiwan cohort, while VA patients were likely tested based on liver disease/risk factors, which may confound HCC outcomes. The German cohort with no HCC after 44 years is most comparable to the CHIM participants. Although it is difficult to precisely estimate HCC risk from an HCV CHIM, the data suggest the risk to be very low or negligible.

Funder

Toronto General Research Institute

US National Institutes of Health

Johns Hopkins University

CIHR

Canadian Network on Hepatitis C

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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