Abstract

BackgroundNovel direct-acting antiviral DAA combination therapies tremendously improved sustained virologic response (SVR) rates in patients with chronic HCV infection. SVR is typically accompanied by normalization of liver enzymes, however, hepatic inflammation, i.e. persistently elevated aminotransferase levels may persist despite HCV eradication. Aim: To investigate prevalence and risk factors for ongoing hepatic inflammation after SVR in two large patient cohorts.MethodsThis post-hoc analysis was based on prospectively collected demographic and clinical data from 834 patients with SVR after HCV treatment with either PegIFN- or DAA-based treatment regimens from the PRAMA trial (n = 341) or patients treated at our outpatient clinic (n = 493).ResultsWe observed an unexpected high prevalence of post-SVR inflammation, including patients who received novel IFN-free DAA-based therapies. Up to 10% of patients had ongoing elevation of aminotransferase levels and another 25% showed aminotransferase activity above the so-called healthy range. Several baseline factors were independently associated with post-SVR aminotransferase elevation. Among those, particularly male gender, advanced liver disease and markers for liver steatosis were strongly predictive for persistent ALT elevation. The use of IFN-based antiviral treatment was independently correlated with post-SVR inflammation, further supporting the overall benefit of IFN-free combination regimens.ConclusionThis is the first comprehensive study on a large patient cohort investigating the prevalence and risk factors for ongoing liver inflammation after eradication of HCV. Our data show a high proportion of patients with ongoing hepatic inflammation despite HCV eradication with potential implications for the management of approximately one third of all patients upon SVR.

Highlights

  • Sustained virological response (SVR), defined as undetectable serum hepatitis C virus ribonucleic acid (RNA) (HCV-RNA) 12 to 24 weeks after the end of treatment, is the primary goal of antiviral therapy in patients with hepatitis C

  • SVR is typically accompanied by normalization of liver enzymes, hepatic inflammation, i.e. persistently elevated aminotransferase levels may persist despite HCV eradication

  • Male gender, advanced liver disease and markers for liver steatosis were strongly predictive for persistent alanine aminotransferase (ALT) elevation

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Summary

Introduction

Sustained virological response (SVR), defined as undetectable serum hepatitis C virus RNA (HCV-RNA) 12 to 24 weeks after the end of treatment, is the primary goal of antiviral therapy in patients with hepatitis C. The recent introduction of numerous directly acting antiviral agents (DAAs) against HCV enabled interferon-free, all-oral regimens which achieve SVR rates of at least 90% [1,2]. SVR is typically accompanied by normalization of aminotransferases (ALT, AST) as surrogate markers for hepatic inflammation, considered as patient relevant endpoint with a 60–80% reduction in the development of cirrhosis and hepatocellular carcinoma (HCC), respectively [3]. Novel direct-acting antiviral DAA combination therapies tremendously improved sustained virologic response (SVR) rates in patients with chronic HCV infection. SVR is typically accompanied by normalization of liver enzymes, hepatic inflammation, i.e. persistently elevated aminotransferase levels may persist despite HCV eradication. Aim: To investigate prevalence and risk factors for ongoing hepatic inflammation after SVR in two large patient cohorts

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