Liver-related events and mortality among elderly patients with advanced chronic hepatitis C treated with direct-acting antivirals
Identifiers
Identifiers
Date issued
2019Journal title
PLoS One
Type of content
Artigo
DeCS
carcinoma | anciano | antivíricos | hígado | hepatitis C | mediana edad | humanos | neoplasias hepáticas | carcinogénesisMeSH
Hepatitis C | Carcinoma | Middle Aged | Humans | Carcinogenesis | Liver | Liver Neoplasms | Aged | Antiviral AgentsAbstract
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.