Skip to main navigation Skip to search Skip to main content

Persistent risk of hepatocellular carcinoma despite improvement of liver stiffness in patients with chronic HBV with advanced fibrosis

  • Lesley A. Patmore*
  • , Lilian Y. Liang
  • , George Papatheodoridis
  • , Mai Kilany
  • , Arno Furquim d'Almeida
  • , Vincent W. S. Wong
  • , Margarita Papatheodoridi
  • , Thomas Vanwolleghem
  • , Pieter Honkoop
  • , Hans Blokzijl
  • , Özgür M. Koc
  • , Harry L. A. Janssen
  • , Matthijs Kramer
  • , Joep de Bruijne
  • , Apichat Kaewdech
  • , Robert A. de Man
  • , R. Bart Takkenberg
  • , Grace L. H. Wong
  • , Jordan J. Feld
  • , Milan J. Sonneveld
  • *Corresponding author for this work
  • Erasmus University Rotterdam
  • Chinese University of Hong Kong
  • National and Kapodistrian University of Athens
  • UHN - Toronto General Hospital
  • University of Antwerp
  • Albert Schweitzer Ziekenhuis
  • University of Groningen
  • Maastricht University
  • Utrecht University
  • Prince of Songkla University
  • Amsterdam UMC - University of Amsterdam

Research output: Contribution to journalArticleAcademicpeer-review

91 Downloads (Pure)

Abstract

Background & Aims: Patients with chronic HBV (CHB) with advanced fibrosis are at high risk for hepatocellular carcinoma (HCC). Liver stiffness measurement (LSM) correlates with fibrosis in untreated patients, and is used to monitor changes in severity of liver disease. However, the association between on-treatment LSM and HCC risk is controversial. Methods: We conducted an international multicenter retrospective cohort study of patients with CHB with advanced fibrosis and assessed the association between on-treatment LSM, HCC development, and decompensation events. Results: We analyzed 562 patients (62.8% F4 LSM measurement, 69.2% Asian). During antiviral therapy, the on-treatment LSM decreased to <6 kPa in 209 (37.2%), to 6–9 kPa in 174 (31.0%), and remained >9 kPa in 179 (31.9%) patients. During a median follow-up of 6.8 years after the on-treatment LSM, 56 patients developed HCC and 18 (32.2%) had an on-treatment LSM <6 kPa. The 5-year cumulative HCC incidence was comparable across on-treatment LSM strata; 4.4% for <6 kPa, 5.5% for 6–9 kPa, and 5.8% for >9 kPa (p = 0.300). In multivariable analysis, older age (adjusted hazard ratio (aHR) 1.058, 95% CI 1.026–1.091, p <0.001) and lower platelet count (aHR 0.992, 95% CI 0.992–0.998, p = 0.005) were associated with HCC development, whereas on-treatment LSM was not (aHR 0.974, p = 0.974). By contrast, patients with an LSM decrease to ≤9 kPa had a negligible risk of decompensation (0% vs. 1.8% at 5 years, p = 0.017). Conclusions: Most patients with CHB with advanced fibrosis experienced a decrease in LSM during antiviral therapy. Although a decrease in liver stiffness was associated with a lower risk of decompensation, an improvement in liver stiffness was not associated with a reduction in HCC risk. Impact and implications: The majority of CHB patients with advanced fibrosis have a decrease in LSM during antiviral therapy. Although a decrease in LSM was associated with a lower risk of subsequent hepatic decompensation, an improvement in LSM was not associated with a reduction in HCC risk. HCC surveillance should therefore be continued in patients with advanced fibrosis at baseline regardless of LSM values obtained during therapy.

Original languageEnglish
Article number101560
JournalJHEP Reports
Volume7
Issue number11
DOIs
Publication statusPublished - 1 Nov 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • ACLD
  • Advanced chronic liver disease
  • Cirrhosis
  • LSM
  • Vibration-controlled transient elastography

Fingerprint

Dive into the research topics of 'Persistent risk of hepatocellular carcinoma despite improvement of liver stiffness in patients with chronic HBV with advanced fibrosis'. Together they form a unique fingerprint.

Cite this