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Review
. 2024 Dec;44(12):3138-3150.
doi: 10.1111/liv.16113. Epub 2024 Sep 30.

Follow-up post-HCV virological response to DAA in advanced chronic liver disease

Affiliations
Review

Follow-up post-HCV virological response to DAA in advanced chronic liver disease

A Romano et al. Liver Int. 2024 Dec.

Abstract

Direct-acting antivirals (DAA) achieve high virological response rates with minimal side effects for many patients. Despite their significant impact on the progression and epidemiology of hepatitis C virus (HCV) associated liver disease, the global annual incidence of chronic infections is expected to remain relatively constant, averaging 1.42 million new cases each year until 2030. Furthermore, by 2030, there will be a 14-17% increase in end-stage liver disease outcomes such as liver-related deaths, hepatocellular carcinoma (HCC), and decompensated cirrhosis in adults aged 18 years and over. Although reductions in liver decompensation, HCC occurrence, and mortality have been shown in patients with advanced liver disease who achieved sustained virological response (SVR) with DAA, these benefits may be less significant in those with decompensated liver cirrhosis. This review aims to summarise the impact of the virological response to DAA on liver disease progression and outcomes in patients with advanced chronic liver disease, which appears to be crucial for defining patient-specific follow-up.

Keywords: advanced chronic liver disease; chronic hepatitis C; sustained virological response.

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References

REFERENCES

    1. Stanciu C, Muzica CM, Girleanu I, et al. An update on direct antiviral agents for the treatment of hepatitis C. Expert Opin Pharmacother. 2021;22:1729‐1741.
    1. GBD 2017 Cirrhosis Collaborators. The global, regional, and national burden of cirhosis by cause in 195 countries and territories, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet Gastroenterol Hepatol. 2020;5:245‐266.
    1. Polaris Observatory HCV Collaborators. Global change in hepatitis C virus prevalence and cascade of care between 2015 and 2020: a modelling study. Lancet Gastroenterol Hepatol. 2022;7:396‐415.
    1. Tada T, Kurosaki M, Nakamura S, et al. Real‐world clinical outcomes of sofosbuvir and velpatasvir treatment in HCV genotype 1‐ and 2‐infected patients with decompensated cirrhosis: a nationwide multicenter study by the Japanese red cross liver study group. J Med Virol. 2021;93:6247‐6256.
    1. Carrat F, Fontaine H, Dorival C, et al. Clinical outcomes in patients with chronic hepatitis C after direct‐acting antiviral treatment: a prospective cohort study. Lancet. 2019;393:1453‐1464.

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