Lower hepatocellular carcinoma surveillance in metabolic dysfunction‐associated steatotic liver disease: Impact on treatment eligibility

Author:

Henry‐Blake Connor1,Balachandrakumar Vinay1,Kassab Mohamed1,Devonport Joshua1,Matthews Charmaine1,Fox James1,Baggus Elisabeth1,Henney Alexander234,Stern Nicholas1,Cuthbertson Daniel J234,Palmer Daniel5,Johnson Philip J5,Hughes David M6,Hydes Theresa J134ORCID,Cross Timothy J S15

Affiliation:

1. Department of Gastroenterology and Hepatology Liverpool University Hospitals NHS Foundation Trust Liverpool UK

2. Department of Diabetes and Endocrinology Liverpool University Hospitals NHS Foundation Trust Liverpool UK

3. Department of Cardiovascular and Metabolic Medicine University of Liverpool Liverpool UK

4. Liverpool Centre for Cardiovascular Sciences University of Liverpool and Liverpool University Hospitals NHS Foundation Trust Liverpool UK

5. Department of Molecular and Clinical Cancer Medicine University of Liverpool Liverpool UK

6. Department of Health Data Science, Institute of Population Health University of Liverpool Liverpool UK

Abstract

AbstractBackground and AimThis study aimed to compare the determinants and impact of hepatocellular carcinoma (HCC) surveillance rates for people with metabolic dysfunction‐associated steatotic liver disease (MASLD) versus other chronic liver diseases.MethodsA dataset of HCC patients from a UK hospital (2007–2022) was analyzed. The Mann–Whitney U‐test compared continuous variables. The χ2 and two‐tailed Fisher exact tests compared categorical data. Regression modeling analyzed the impact of MASLD on the size and number of HCC nodules and curative treatment. The Cox proportional hazards model assessed the influence of MASLD on overall survival.ResultsA total of 176 of 687 (25.6%) HCC patients had MASLD. Fewer people with MASLD HCC were enrolled in HCC surveillance compared to non‐MASLD HCC (38 [21.6%] vs 215 [42.1%], P < 0.001). Patients with MASLD HCC were less likely to have been under secondary care (n = 57 [32.4%] vs 259 [50.7%], P < 0.001) and less likely to have cirrhosis (n = 113 [64.2%] vs 417 [81.6%], P < 0.001). MASLD was associated with a 12.3‐mm (95% confidence interval [CI] 10.8–14.0 mm) greater tumor diameter compared to people without MASLD (P = 0.002). Patients with MASLD HCC had 0.62 reduced odds (95% CI 0.43–0.91) of receiving curative treatment compared to non‐MASLD HCC (P = 0.014). Overall survival was similar for patients with MASLD HCC versus non‐MASLD HCC (hazard ratio 1.03, 95% CI 0.85–1.25, P = 0.748).ConclusionPatients with MASLD are less likely to have been enrolled in HCC surveillance due to undiagnosed cirrhosis or presenting with non‐cirrhotic HCC. Patients with MASLD HCC present with larger tumors and are less likely to receive curative treatment.

Publisher

Wiley

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