Evidence map›Paper›PMID 41143239›Full record

ArticleJHEP reports : innovation in hepatology2025

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 and 10 more

Abstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Lesley A PatmoreDepartment of Gastroenterology and Hepatology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Lilian Y LiangMedical Data Analytics Centre, Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong Special Administrative Region of China.
George PapatheodoridisDepartment of Gastroenterology, School of Medicine, National and Kapodistrian University of Athens, Laiko General Hospital Athens, Athens, Greece.
Mai KilanyToronto Centre for Liver Disease, Toronto General Hospital, University of Toronto, Toronto, ONT, Canada.
Arno Furquim d'AlmeidaDepartment of Gastroenterology and Hepatology, Antwerp University Hospital, Antwerp, Belgium.
Vincent W S WongMedical Data Analytics Centre, Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong Special Administrative Region of China.
Margarita PapatheodoridiDepartment of Gastroenterology, School of Medicine, National and Kapodistrian University of Athens, Laiko General Hospital Athens, Athens, Greece.
Thomas VanwolleghemDepartment of Gastroenterology and Hepatology, Antwerp University Hospital, Antwerp, Belgium.
Pieter HonkoopDepartment of Gastroenterology and Hepatology, Albert Schweitzer Hospital, Dordrecht, The Netherlands.
Hans BlokzijlDepartment of Gastroenterology and Hepatology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Özgür M KocDepartment of Gastroenterology and Hepatology, Maastricht University Medical Center, Maastricht, The Netherlands.
Harry L A JanssenDepartment of Gastroenterology and Hepatology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Matthijs KramerDepartment of Gastroenterology and Hepatology, Maastricht University Medical Center, Maastricht, The Netherlands.
Joep de BruijneDepartment of Gastroenterology and Hepatology, Utrecht UMC, Utrecht, The Netherlands.
Apichat KaewdechGastroenterology and Hepatology Unit, Division of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand.
Robert A de ManDepartment of Gastroenterology and Hepatology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
R Bart TakkenbergDepartment of Gastroenterology and Hepatology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
Grace L H WongMedical Data Analytics Centre, Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong Special Administrative Region of China.
Jordan J FeldToronto Centre for Liver Disease, Toronto General Hospital, University of Toronto, Toronto, ONT, Canada.
Milan J SonneveldDepartment of Gastroenterology and Hepatology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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 ( 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.

Indexed as

ACLDAdvanced chronic liver diseaseCirrhosisLSMVibration-controlled transient elastography

Identifiers

PMID41143239
PMCPMC12550779

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.