Molecular Mechanisms Involved in HCC Recurrence after Direct-Acting Antiviral Therapy

Int J Mol Sci. 2018 Dec 22;20(1):49. doi: 10.3390/ijms20010049.

Abstract

Chronic hepatitis C is associated with a high risk of developing hepatocellular carcinoma (HCC) because of a direct effect of the Hepatitis C Virus (HCV) proteins and an indirect oncogenic effect of chronic inflammation and impaired immune response. The treatment of chronic hepatitis C markedly reduces all-cause mortality; in fact, interferon-based treatment has shown a reduction of HCC incidence of more than 70%. The recent introduction of the highly effective direct-acting antivirals (DAAs) has completely changed the scenario of chronic hepatitis C (CHC) with rates of HCV cure over 90%. However, an unexpectedly high incidence of HCC recurrence was observed in patients after DAA treatment (27% versus 0.4⁻2% in patients who received interferon treatment). The mechanism that underlies the high rate of tumor relapse is currently unknown and is one of the main issues in hepatology. We reviewed the possible mechanisms involved in HCC recurrence after DAA treatment.

Keywords: direct-acting antivirals; hepatocellular carcinoma.

Publication types

  • Review

MeSH terms

  • Animals
  • Antiviral Agents / therapeutic use*
  • Carcinoma, Hepatocellular / drug therapy*
  • Carcinoma, Hepatocellular / epidemiology
  • Carcinoma, Hepatocellular / immunology
  • Carcinoma, Hepatocellular / virology
  • Hepacivirus / drug effects
  • Hepacivirus / immunology
  • Hepatitis C, Chronic / drug therapy*
  • Hepatitis C, Chronic / epidemiology
  • Hepatitis C, Chronic / immunology
  • Hepatitis C, Chronic / virology
  • Humans
  • Incidence
  • Interferons / therapeutic use
  • Liver Neoplasms / drug therapy*
  • Liver Neoplasms / epidemiology
  • Liver Neoplasms / immunology
  • Liver Neoplasms / virology
  • Macrophages / drug effects
  • Monocytes / drug effects
  • Neoplasm Recurrence, Local / drug therapy*
  • Neoplasm Recurrence, Local / epidemiology
  • Neoplasm Recurrence, Local / immunology
  • Neoplasm Recurrence, Local / virology
  • Neutrophils / drug effects

Substances

  • Antiviral Agents
  • Interferons