Abstract

BackgroundInterferon-α/ribavirin combination therapy might promote hepatitis B surface antigen (HBsAg) seroclearance in patients dually infected with hepatitis B and C viruses (HBV/HCV), but the long-term effect remains unclear. We aimed to investigate the rate of and the factors associated with HBsAg seroclearance during long-term follow-up after interferon-α/ribavirin combination therapy in HBV/HCV dually-infected patients.Methodology/Principal FindingsEighty-one patients who received interferon-α/ribavirin combination therapy for 24 weeks with a follow-up period of >24 weeks were enrolled. HBV serological markers and HBV DNA were determined every 6 months. Early and late HBsAg seroclearance were defined as HBsAg loss in less or more than 6 months after end-of-treatment, respectively. Fifteen (18.5%) patients had HBsAg seroclearance during a mean follow-up period of 3.4 (0.5–5.1) years. The 5-year cumulative incidence was 25.6%. Baseline cirrhosis and HBV DNA negativity 1 year after end-of-treatment were independently predictive of HBsAg seroclearance with an odds ratio (OR), 95% confidence intervals (CI) of 16.6, 1.8–153 and 9.2, 1.4–62.1, respectively, by Cox regression hazard analysis. Four patients developed early and 11 developed late HBsAg seroclearance, respectively. Cox regression hazard analysis showed no factor was associated with early HBsAg seroclearance, whilst HBV DNA negativity 1 year after end-of-treatment was the only significant factor predicting late HBsAg loss (OR, 43.0; CI, 2.5–745). Five patients had HBsAg seroconversion with a 5-year cumulative incidence of 8.3%. HBV DNA negativity at baseline and one year after EOT had a trend for HBsAg seroconversion. HCV response did not correlate to HBsAg loss.ConclusionsWe demonstrated that interferon-α/ribavirin had long-term effect on HBsAg seroclearance in dually HBV/HCV-infected patients. Baseline cirrhosis and seroclearance of HBV DNA 1 year after end-of-treatment were significant factors associated with HBsAg seroclearance.

Highlights

  • Hepatitis B virus (HBV) and hepatitis C virus (HCV) infections are the two leading causes of chronic liver disease, liver cirrhosis (LC), and hepatocellular carcinoma (HCC) [1,2]

  • We demonstrated that interferon-a/ribavirin had long-term effect on hepatitis B surface antigen (HBsAg) seroclearance in dually HBV/HCVinfected patients

  • Baseline cirrhosis and seroclearance of HBV DNA 1 year after end-of-treatment were significant factors associated with HBsAg seroclearance

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Summary

Introduction

Hepatitis B virus (HBV) and hepatitis C virus (HCV) infections are the two leading causes of chronic liver disease, liver cirrhosis (LC), and hepatocellular carcinoma (HCC) [1,2]. HBsAg seroclearance is very rarely observed in HBV infected patients receiving current antiviral agents, with an annual rate of 2.4–3.2% with interferon (IFN) or pegylated IFN therapy and only ,1% with nucleoside/nucleotide analogues [11,12]. Interferon-a/ribavirin combination therapy might promote hepatitis B surface antigen (HBsAg) seroclearance in patients dually infected with hepatitis B and C viruses (HBV/HCV), but the long-term effect remains unclear. We aimed to investigate the rate of and the factors associated with HBsAg seroclearance during long-term follow-up after interferon-a/ ribavirin combination therapy in HBV/HCV dually-infected patients

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