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Long-term risk of HCC in a DAA-treated national hepatitis C cohort, and a proposed risk score
Örebro University, School of Medical Sciences. Örebro University Hospital. Department of Infectious Diseases.ORCID iD: 0000-0001-6711-0499
Cytel Inc, Stockholm, Sweden.
Cytel Inc, Stockholm, Sweden; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Örebro University, School of Medical Sciences. Clinical Epidemiology and Biostatistics, School of Medical Sciences, Örebro University, Örebro, Sweden; Clinical Epidemiology Division, Karolinska Institutet, Stockholm, Sweden; Department of Epidemiology and Public Health, University College London, London, United Kingdom.ORCID iD: 0000-0001-6328-5494
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2025 (English)In: Infectious Diseases, ISSN 2374-4235, E-ISSN 2374-4243, Vol. 57, no 3, p. 211-233Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: The risk of hepatocellular carcinoma (HCC) remains elevated in cirrhotic hepatitis C patients with sustained virological response (SVR) after DAA treatment. We assessed long-term HCC risk stratified by pretreatment liver stiffness measurement (LSM) and developed a risk score algorithm.

METHODS: This register-based nationwide cohort study of 7,227 DAA-treated patients with SVR evaluated annual HCC incidence rates (IRs) and cumulative incidences stratified by pretreatment LSM. The association between LSM and HCC risk was analyzed using multivariate Cox regression. A risk score algorithm was developed and internally validated in 2,664 individuals with LSM >9.5 kPa, assigning each patient a score based on risk factors, proportionally weighted by the association with HCC risk.

RESULTS: During a median follow-up of 1.8 years (3.2 years for LSM ≥12.5 kPa), 92 patients (1.3%) developed HCC. The IRs for LSM 9.5-12.4, 12.5-19.9 and ≥20 kPa were 0.21, 0.99 and 2.20 HCC/100 PY, respectively, with no significant risk reduction during follow-up. The HRs (and 95% CI) for LSM 9.5-12.5, 12.5-19.9 and ≥20 kPa are 1.19 (0.43-3.28), 4.66 (2.17-10.01) and 10.53 (5.26-21.08), respectively. Risk score models including FIB-4, alcohol, diabetes, age and LSM effectively stratified patients with LSM >9.5 kPa into low-, intermediate- and high-risk groups, with a Harrell's C of 0.799. Notably, 48% with LSM ≥9.5 kPa and 27% ≥12.5 kPa were classified as low-risk.

CONCLUSION: Pretreatment LSM is associated with HCC risk, which remains stable during the initial five years post-SVR. The HCC risk score algorithm effectively identifies low-risk patients, who may not require HCC surveillance.

Place, publisher, year, edition, pages
Taylor & Francis, 2025. Vol. 57, no 3, p. 211-233
Keywords [en]
DAA, HCC, Viral hepatitis, risk score, surveillance
National Category
Gastroenterology and Hepatology
Identifiers
URN: urn:nbn:se:oru:diva-116332DOI: 10.1080/23744235.2024.2403703ISI: 001320043200001PubMedID: 39319565Scopus ID: 2-s2.0-85204781971OAI: oai:DiVA.org:oru-116332DiVA, id: diva2:1901119
Funder
Region StockholmNyckelfonden, OLL-691511Region Örebro County, OLL-930212; OLL-880331; OLL-961427; OLL-691511Swedish Cancer SocietyAvailable from: 2024-09-26 Created: 2024-09-26 Last updated: 2025-03-24Bibliographically approved

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Lybeck, CharlotteMontgomery, ScottDuberg, Ann-Sofi

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