Outcomes of liver transplantation in non-alcoholic steatohepatitis (NASH) versus non-NASH associated hepatocellular carcinoma

  • Luckshi Rajendran
  • , Carla F. Murillo Perez
  • , Tommy Ivanics
  • , Marco P.A.W. Claasen
  • , Bettina E. Hansen
  • , David Wallace
  • , Peter D. Yoon
  • , Gonzalo Sapisochin*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

12 Citations (Scopus)
10 Downloads (Pure)

Abstract

Background: Non-alcoholic steatohepatitis (NASH)-associated hepatocellular carcinoma (HCC) is a rising indication for liver transplantation. This unique population, with multiple comorbidities, has potential for worse post-transplant outcomes. We compared post-transplant survival of NASH and non-NASH HCC patients using a large cohort. Methods: Adults transplanted for HCC between 2008 and 2018, from United Network for Organ Sharing (UNOS) and University Health Network (UHN) databases were divided into two populations: NASH and non-NASH. Recipient characteristics and post-transplant survival were compared. Subgroup analyses were performed within and beyond Milan criteria. Results: 2071 of 20,672 (10.0%) patients underwent transplantation for NASH HCC, with annual proportional increase of 1.2%UHN (p = 0.02) and 1.3%UNOS (p < 0.001). The 1-,3-,5-year post-transplant survival were 90.8%, 83.9%, 76.3% NASH HCC versus 91.9%, 82.1%, 74.9% non-NASH HCC (p = 0.94). No survival differences were observed in populations within or beyond Milan. Competing-risk analysis demonstrated no differences in risk for cardiovascular-related death (HR1.24, 95%CI 0.87–1.55, p = 0.16), or HCC recurrence-related death (HR1.21, 95%CI 0.89–1.65, p = 0.23). NASH HCC patients had lower risk of liver-related deaths (HR0.57, 95%CI 0.34–0.98, p = 0.04). Discussion: NASH HCC is a rising indication for liver transplantation. Despite demographic differences, no post-transplantation survival differences were observed between NASH and non-NASH HCC. This justifies equivalent organ allocation, irrespective of NASH status.

Original languageEnglish
Pages (from-to)556-567
Number of pages12
JournalHPB
Volume25
Issue number5
Early online dateFeb 2023
DOIs
Publication statusPublished - May 2023

Bibliographical note

Funding Information:
This work was a poster presentation at the 2022 International Hepato-Pancreatico-Biliary Association (IHPBA) World Congress, and an oral presentation at the 2022 International Liver Cancer Association (ILCA).

Publisher Copyright:
© 2023 International Hepato-Pancreato-Biliary Association Inc.

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