Prognostic performance of the two-step clinical care pathway in metabolic dysfunction-associated steatotic liver disease
- PMID: 39863175
- DOI: 10.1016/j.jhep.2025.01.014
Prognostic performance of the two-step clinical care pathway in metabolic dysfunction-associated steatotic liver disease
Abstract
Background & aims: Current guidelines recommend a two-step approach for risk stratification in patients with metabolic dysfunction-associated steatotic liver disease (MASLD) involving Fibrosis-4 index (FIB-4) followed by liver stiffness measurement (LSM) by vibration-controlled transient elastography (VCTE) or similar second-line tests. This study aimed to examine the prognostic performance of this approach.
Methods: The VCTE-Prognosis study was a longitudinal study of patients with MASLD who had undergone VCTE examinations at 16 centres from the US, Europe and Asia with subsequent follow-up for clinical events. The primary endpoint was incident liver-related events (LREs), defined as hepatic decompensation and/or hepatocellular carcinoma.
Results: Of 12,950 patients (mean age 52 years, 41% female, 12.1% LSM >12 kPa), baseline FIB-4, at cut-offs of 1.3 (or 2.0 for age ≥65) and 2.67, classified 66.3% as low-risk and 9.8% as high-risk, leaving 23.9% in the intermediate-risk zone. After classifying intermediate FIB-4 patients as low-risk if LSM was <8.0 kPa and high-risk if LSM was >12.0 kPa, 81.5%, 4.6%, and 13.9% of the full cohort were classified as low-, intermediate-, and high-risk, respectively. At a median (IQR) follow-up of 47 (23-72) months, 248 (1.9%) patients developed LREs. The 5-year cumulative incidence of LREs was 0.5%, 1.0% and 10.8% in the low-, intermediate- and high-risk groups, respectively. Replacing LSM with Agile 3+, Agile 4, and FAST did not reduce the intermediate-risk zone or improve event prediction. Classifying intermediate FIB-4 patients by LSM <10 kPa (low-risk) and >15 kPa (high-risk) reduced the intermediate-risk zone while maintaining predictive performance.
Conclusions: The non-invasive two-step approach of FIB-4 followed by LSM is effective in classifying patients at different risks of LREs.
Impact and implications: Metabolic dysfunction-associated steatotic liver disease (MASLD) is emerging as one of the leading causes of cirrhosis and hepatocellular carcinoma worldwide, but only a minority of patients will develop these complications. Therefore, it is necessary to use non-invasive tests instead of liver biopsy for risk stratification. Additionally, as most patients with MASLD are seen in primary care instead of specialist settings, cost and availability of the tests should be taken into consideration. In this multicentre study, the use of the Fibrosis-4 index followed by liver stiffness measurement by vibration-controlled transient elastography effectively identified patients who would later develop liver-related events. The results support current recommendations by various regional guidelines on a clinical care pathway based on non-invasive tests to diagnose advanced liver fibrosis.
Keywords: FIB-4; Hepatocellular carcinoma; MASLD; VCTE; hepatic decompensation.
Copyright © 2025 The Author(s). Published by Elsevier B.V. All rights reserved.
Conflict of interest statement
Conflict of interest ET served as a consultant for Pfizer, NovoNordisk, Boehringer, and Siemens Healthineers; and a speaker for NovoNordisk, Echosens, and Dr Falk. SP served as a speaker or advisor for AbbVie, Echosens, MSD, Novo Nordisk, Pfizer, and Resalis. EB served as a consultant for Boehringer, MSD, Novo Nordisk, and Pfizer; and a speaker for MSD, Novo Nordisk, and Madrigal. She received research grants from Gilead Sciences. MY received research grant from Gilead Sciences and speaker for KOWA. AN received research grants from Mochida Pharmaceutical, Astellas Pharma, ASKA pharmaceutical, Biofermin Pharmaceutical and EA pharma; a speaker for Mochida Pharmaceutical, Kowa, Biofermin Pharmaceutical, MSD, Boehringer, Novo Nordisk, GlaxoSmithkline, EA pharma. HH served as a consultant for AstraZeneca; and a hepatic events adjudication committee member for KOWA and GW Pharama. His institution has received research funding from AstraZeneca, Echosens, Gilead Sciences, Intercept, MSD, and Pfizer. JB served as a consultant for AstraZeneca, Echosens, Intercept, and Siemens; a speaker for AbbVie, Gilead Sciences, Intercept, and Siemens; and an advisory board member for Bristol-Myers-Squibb, Intercept, Pfizer, MSD, and Novo Nordisk. His institution has received research funding from Diafir, Echosens, Intercept, Inventiva, and Siemens. JLC served as a consultant and speaker for Echosens, Gilead Sciences, and AbbVie. GB-BG served as a consultant for Roche and Ionis Pharmaceuticals; and a speaker for Echosens, Viatris, Abbott and Novo Nordisk. WKC served as a consultant for Abbott, Roche, AbbVie, Novo Nordisk, and Boehringer Ingelheim; and a speaker for Abbott, Novo Nordisk, Echosens, Hisky Medical, and Viatris. AJS served as a consultant for 89Bio, Akero, Allergan, Alnylam Pharmaceuticals, Amgen Inc, AstraZeneca, Boehringer Ingelheim, Bristol-Myers Squibb, Genentech, Gilead Sciences, Histoindex, Intercept Pharmaceuticals, Inventiva, Madrigal, Merck, Novartis, Novo Nordisk, Pfizer, Poxel, Salix Pharmaceuticals, Siemens, Sun Pharmaceutical Industries Inc, Terns, and Valeant Pharmaceuticals; and a data safety monitoring board or advisory board member for Bard Peripheral Vascular Inc, NGM Biopharmaceuticals, and Sequana. He has received research funding from Albireo, Allergan, Echosens, Eli Lilly, Gilead Sciences, Intercept Pharmaceuticals, Mallinckrodt LLC, Merck, Novo Nordisk, Perspectum, Pfizer, Salix Pharmaceuticals, and Zydus; and holds the stocks of Durect, Exhalenz, Gen t, and Tiziana. MR-G served as a consultant for Siemens; and a speaker for Siemens and Echosens. He has received research funding from Siemens, Echosens, and Novo Nordisk. PN served as a consultant for Novo Nordisk, Boehringer Ingelheim, Gilead Sciences, Intercept, Poxel Pharmaceuticals, Pfizer, BMS, Eli Lilly, Madrigal, and GSK; and a speaker for Novo Nordisk and AiCME. He has received research funding from Novo Nordisk. LC served as a consultant for Boston pharmaceutical, Echosens, Gilead, GSK, Madrigal, MSD, Novo Nordisk, Pfizer, Sagimet and Siemens Healthineers and as speaker for Echosens, Gilead, Inventiva, Madrigal and Novo Nordisk. CF-P is an employee of Echosens. GL-HW served as a consultant for AstraZeneca, Gilead Sciences, GlaxoSmithKline and Janssen; and a speaker for Abbott, Abbvie, Bristol-Myers Squibb, Echosens, Furui, Gilead Sciences, GlaxoSmithKline and Roche. She has received research funding from Gilead Sciences. MS-WC is an employee of Echosens. VW-SW served as a consultant or advisory board member for AbbVie, Boehringer Ingelheim, Echosens, Gilead Sciences, Intercept, Inventiva, Novo Nordisk, Pfizer, Sagimet Biosciences, TARGET PharmaSolutions, and Visirna; and a speaker for Abbott, AbbVie, Gilead Sciences, Novo Nordisk, and Unilab. He has received a research grant from Gilead Sciences, and is a co-founder of Illuminatio Medical Technology. Please refer to the accompanying ICMJE disclosure forms for further details.
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