Annals of Hepatology (Nov 2020)

LI-RADS 4 or 5 categorization may not be clinically relevant for decision-making processes: A prospective cohort study

  • Federico Piñero,
  • Marcos A. Thompson,
  • Federico Diaz Telli,
  • Juan Trentacoste,
  • Carlos Padín,
  • Manuel Mendizabal,
  • Carla Colaci,
  • Ariel Gonzalez Campaña,
  • Josefina Pages,
  • Silvina Montal,
  • Mariano Barreiro,
  • Martín Fauda,
  • Gustavo Podestá,
  • Juan Pablo Perotti,
  • Marcelo Silva

Journal volume & issue
Vol. 19, no. 6
pp. 662 – 667

Abstract

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Introduction and objectives: The liver imaging reporting data system (LI-RADS) for hepatocellular carcinoma (HCC) was proposed to standardize and enhance consensus of reporting. However, clinical utility of LI-RADS has not been evaluated in Latin America. We therefore sought to compare LI-RADS categories with histopathology findings in liver transplant (LT) explants in a regional center. Materials and methods: Prospective cohort study conducted between 2012 and 2018 in a single center from Argentina including patients with HCC listed for LT. LI-RADS definitions were applied to magnetic resonance images (MRI) or computed tomography (CT) abdominal scans at time of listing and at final pre-LT reassessment and compared to explant pathology findings; specifically, major nodule (NOD1). Results: Of 130 patients with HCC listed for LT (96.1% with cirrhosis and 35.6% with hepatitis C virus infection), 72 underwent LT. Overall, 65% had imaging HCC diagnosis based on MRI (n = 84), 26% with CT (n = 34) and 9% (n = 12) with both methods. Among LT patients with pre-transplant imaging at our institution (n = 42/72), 69% of the NOD1 were LR-5, 21% LR-4 and 10% LR-3. Definite HCC diagnosis was 50% in LR-3 NOD1 (CI 18–90); none presented microvascular invasion. In LR-4 NOD1, HCC was confirmed in 89% (CI 59–98), of which 11% showed microvascular invasion; whereas in LR-5 NOD1 77% (CI 64–87) had confirmed HCC, 17% with microvascular invasion. Conclusions: LI-RADS was useful to standardize reports; however, no significant differences were observed between LR-4 and LR-5 HCC probability when compared to explant pathology.

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