Liver-related events and mortality among elderly patients with advanced chronic hepatitis C treated with direct-acting antivirals

PLoS One. 2019 Jun 3;14(6):e0217052. doi: 10.1371/journal.pone.0217052. eCollection 2019.

Abstract

Background: Direct-acting antivirals (DAAs) are effective in patients aged ≥65 years. However, little is known about the effects of DAAs on survival, liver decompensation and development of hepatocellular carcinoma (HCC).

Objective: To compare the incidence of liver-related events and mortality between patients aged ≥65 and <65 years.

Methods: Prospective study comparing patients aged ≥65 and <65 years treated with DAAs. The incidence of liver-related events and mortality, and HCC was compared between age groups.

Results: Five hundred patients (120 aged ≥65 and 380 aged <65 years) were included. The incidence of liver-related events was 2.62 per 100 patient-years (py) in older and 1.41/100 py in younger patients. All-cause mortality was 3.89 and 1.27/100 py in older and younger patients, respectively. The respective liver-related mortality rates were 1.12 and 0.31/100 py. In patients with cirrhosis (stage F4), all-cause mortality (P = 0.283) and liver-related mortality (P = 0.254) did not differ between groups. All five liver-related deaths were related to multifocal HCC. The incidence of HCC was 1.91 and 1.43 per 100 py in the older and younger groups, respectively (P = 0.747). The diagnosis of HCC was 8 months after the end of treatment.

Conclusions: The incidence of liver-related events and liver-related mortality was low in older people treated with DAAs and was similar to that in younger patients. The extra mortality in people aged ≥65 years treated with DAAs seems to be secondary to non-liver-related causes. These results support the utilization of DAAs in patients aged ≥65 years.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Antiviral Agents / pharmacology*
  • Antiviral Agents / therapeutic use
  • Carcinogenesis
  • Carcinoma, Hepatocellular / complications
  • Carcinoma, Hepatocellular / pathology
  • Female
  • Hepatitis C, Chronic / complications
  • Hepatitis C, Chronic / drug therapy*
  • Hepatitis C, Chronic / mortality*
  • Humans
  • Liver / drug effects*
  • Liver / pathology
  • Liver Neoplasms / complications
  • Liver Neoplasms / pathology
  • Male
  • Middle Aged

Substances

  • Antiviral Agents

Grants and funding

This work was supported in part by grants from Fondo de Investigación Sanitaria (JR17/00028), and Fundación Profesor Novoa Santos, A Coruña.