Elastography is unable to exclude cirrhosis after sustained virological response in HCV-infected patients with

Teresa Broquetas1,2, Paula Herruzo-Pino2, Zoe Mariño3

  • 1Liver Section, Gastroenterology Department, Hospital del Mar, Barcelona, Spain.

Insights

Even after successful hepatitis C treatment, cirrhosis persists in over half of patients with advanced liver disease. Non-invasive tests like transient elastography show poor accuracy for detecting cirrhosis post-treatment, necessitating long-term patient monitoring.

Area of Science:

  • Hepatology
  • Virology
  • Diagnostic Imaging

Background:

  • The correlation between liver fibrosis staging via transient elastography (TE) and outcomes in hepatitis C virus (HCV)-infected patients with compensated advanced chronic liver disease (cACLD) following sustained virological response (SVR) remains unclear.
  • Understanding this relationship is crucial for managing patients post-HCV eradication.

Purpose of the Study:

  • To assess the accuracy of transient elastography (TE) in identifying cirrhosis in patients with compensated advanced chronic liver disease (cACLD) three years after achieving a sustained virological response (SVR) to hepatitis C virus (HCV) treatment.

Main Methods:

  • A prospective, multi-centric study enrolled HCV-cACLD patients prior to direct-acting antiviral (DAA) therapy.
  • The diagnostic accuracy of TE to identify cirrhosis (METAVIR F4) three years post-SVR was evaluated using the area under the receiver operating characteristic curve (AUROC).
  • Liver biopsy, TE, APRI, and FIB-4 scores were assessed before and after treatment.

Main Results:

  • Among 746 patients, 76 underwent liver biopsy 3 years post-SVR, revealing cirrhosis in 41 (53.9%).
  • TE values, APRI, and FIB-4 scores improved post-SVR, but TE accuracy for cirrhosis detection was poor (AUROC=0.75).
  • HCV genotype 3 and pre-treatment TE were significant predictors of cirrhosis post-SVR, while post-SVR TE, APRI, and FIB-4 showed limited diagnostic value.

Conclusions:

  • Cirrhosis is prevalent in over half of HCV-cACLD patients three years after SVR, despite improvements in liver function and non-invasive test scores.
  • The low diagnostic accuracy of non-invasive methods, including TE, APRI, and FIB-4, after SVR highlights the need for continued long-term surveillance in these patients.
  • HCV genotype 3 and baseline TE are crucial factors for predicting long-term fibrosis progression.
Abstract

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