Statin, aspirin and metformin use and risk of hepatocellular carcinoma related outcomes following liver transplantation: A retrospective study.

Aspirin HMG-Co-A reductase Hepatocellular carcinoma Liver transplantation Mammalian target of rapamycin Metformin Statins Transplant oncology

Journal

World journal of transplantation
ISSN: 2220-3230
Titre abrégé: World J Transplant
Pays: United States
ID NLM: 101608356

Informations de publication

Date de publication:
18 Sep 2024
Historique:
received: 28 03 2024
revised: 13 05 2024
accepted: 30 05 2024
medline: 19 9 2024
pubmed: 19 9 2024
entrez: 19 9 2024
Statut: ppublish

Résumé

Liver transplantation (LT) is a potentially curative therapy for patients with hepatocellular carcinoma (HCC). HCC-recurrence following LT is associated with reduced survival. There is increasing interest in chemoprophylaxis to improve HCC-related outcomes post-LT. To investigate whether there is any benefit for the use of drugs with proposed chemoprophylactic properties against HCC, and patient outcomes following LT. This was a retrospective study of adult patients who received Deceased Donor LT for HCC from 2005-2022, from a single Australian centre. Drug use was defined as statin, aspirin or metformin therapy for ≥ 29 days, within 24 months post-LT. A cox proportional-hazards model with time-dependent covariates was used for survival analysis. Outcome measures were the composite-endpoint of HCC-recurrence and all-cause mortality, HCC-recurrence and HCC-related mortality. Sensitivity analysis was performed to account for immortality time bias and statin dosing. Three hundred and five patients were included in this study, with 253 (82.95%) males with a median age of 58.90 years. Aetiologies of liver disease were 150 (49.18%) hepatitis C, 73 (23.93%) hepatitis B (HBV) and 33 (10.82%) non-alcoholic fatty liver disease (NAFLD). 56 (18.36%) took statins, 51 (16.72%) aspirin and 50 (16.39%) metformin. During a median follow-up time of 59.90 months, 34 (11.15%) developed HCC-recurrence, 48 (15.74%) died, 17 (5.57%) from HCC-related mortality. Statin, aspirin or metformin use was not associated with statistically significant differences in the composite endpoint of HCC-recurrence or all-cause mortality [hazard ratio (HR): 1.16, 95%CI: 0.58-2.30; HR: 1.21, 95%CI: 0.28-5.27; HR: 0.61, 95%CI: 0.27-1.36], HCC-recurrence (HR: 0.52, 95%CI: 0.20-1.35; HR: 0.51, 95%CI: 0.14-1.93; HR 1.00, 95%CI: 0.37-2.72), or HCC-related mortality (HR: 0.32, 95%CI: 0.033-3.09; HR: 0.71, 95%CI: 0.14-3.73; HR: 1.57, 95%CI: 0.61-4.04) respectively. Statin dosing was not associated with statistically significant differences in HCC-related outcomes. Statin, metformin or aspirin use was not associated with improved HCC-related outcomes post-LT, in a largely historical cohort of Australian patients with a low proportion of NAFLD. Further prospective, multicentre studies are required to clarify any potential benefit of these drugs to improve HCC-related outcomes.

Sections du résumé

BACKGROUND BACKGROUND
Liver transplantation (LT) is a potentially curative therapy for patients with hepatocellular carcinoma (HCC). HCC-recurrence following LT is associated with reduced survival. There is increasing interest in chemoprophylaxis to improve HCC-related outcomes post-LT.
AIM OBJECTIVE
To investigate whether there is any benefit for the use of drugs with proposed chemoprophylactic properties against HCC, and patient outcomes following LT.
METHODS METHODS
This was a retrospective study of adult patients who received Deceased Donor LT for HCC from 2005-2022, from a single Australian centre. Drug use was defined as statin, aspirin or metformin therapy for ≥ 29 days, within 24 months post-LT. A cox proportional-hazards model with time-dependent covariates was used for survival analysis. Outcome measures were the composite-endpoint of HCC-recurrence and all-cause mortality, HCC-recurrence and HCC-related mortality. Sensitivity analysis was performed to account for immortality time bias and statin dosing.
RESULTS RESULTS
Three hundred and five patients were included in this study, with 253 (82.95%) males with a median age of 58.90 years. Aetiologies of liver disease were 150 (49.18%) hepatitis C, 73 (23.93%) hepatitis B (HBV) and 33 (10.82%) non-alcoholic fatty liver disease (NAFLD). 56 (18.36%) took statins, 51 (16.72%) aspirin and 50 (16.39%) metformin. During a median follow-up time of 59.90 months, 34 (11.15%) developed HCC-recurrence, 48 (15.74%) died, 17 (5.57%) from HCC-related mortality. Statin, aspirin or metformin use was not associated with statistically significant differences in the composite endpoint of HCC-recurrence or all-cause mortality [hazard ratio (HR): 1.16, 95%CI: 0.58-2.30; HR: 1.21, 95%CI: 0.28-5.27; HR: 0.61, 95%CI: 0.27-1.36], HCC-recurrence (HR: 0.52, 95%CI: 0.20-1.35; HR: 0.51, 95%CI: 0.14-1.93; HR 1.00, 95%CI: 0.37-2.72), or HCC-related mortality (HR: 0.32, 95%CI: 0.033-3.09; HR: 0.71, 95%CI: 0.14-3.73; HR: 1.57, 95%CI: 0.61-4.04) respectively. Statin dosing was not associated with statistically significant differences in HCC-related outcomes.
CONCLUSION CONCLUSIONS
Statin, metformin or aspirin use was not associated with improved HCC-related outcomes post-LT, in a largely historical cohort of Australian patients with a low proportion of NAFLD. Further prospective, multicentre studies are required to clarify any potential benefit of these drugs to improve HCC-related outcomes.

Identifiants

pubmed: 39295976
doi: 10.5500/wjt.v14.i3.94914
pmc: PMC11317854
doi:

Types de publication

Journal Article

Langues

eng

Pagination

94914

Informations de copyright

©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict-of-interest statement: Dobrovic A has received honoraria as a speaker from Bio-Rad. Chung W, Wong K, Ravindranayagam N, Tang L, Grace J, Wong D, Con D, Sinclair M, Majumdar A, Kutaiba N, Hui S, Gow P, Muralidharan V and Testro A do not have any conflicts of interests to declare.

Auteurs

William Chung (W)

Department of Gastroenterology, Austin Health, Heidelberg 3084, Victoria, Australia.
Victorian Liver Transplant Unit, Austin Health, Heidelberg 3084, Victoria, Australia. william.chung2@austin.org.au.

Kevin Wong (K)

Department of Gastroenterology, Austin Health, Heidelberg 3084, Victoria, Australia.

Noel Ravindranayagam (N)

Department of Gastroenterology, Austin Health, Heidelberg 3084, Victoria, Australia.

Lauren Tang (L)

Department of Gastroenterology, Austin Health, Heidelberg 3084, Victoria, Australia.
Victorian Liver Transplant Unit, Austin Health, Heidelberg 3084, Victoria, Australia.

Josephine Grace (J)

Department of Gastroenterology, Austin Health, Heidelberg 3084, Victoria, Australia.
Victorian Liver Transplant Unit, Austin Health, Heidelberg 3084, Victoria, Australia.

Darren Wong (D)

Department of Gastroenterology, Austin Health, Heidelberg 3084, Victoria, Australia.
Victorian Liver Transplant Unit, Austin Health, Heidelberg 3084, Victoria, Australia.

Danny Con (D)

Department of Gastroenterology, Austin Health, Heidelberg 3084, Victoria, Australia.

Marie Sinclair (M)

Department of Gastroenterology, Austin Health, Heidelberg 3084, Victoria, Australia.
Victorian Liver Transplant Unit, Austin Health, Heidelberg 3084, Victoria, Australia.

Avik Majumdar (A)

Department of Gastroenterology, Austin Health, Heidelberg 3084, Victoria, Australia.
Victorian Liver Transplant Unit, Austin Health, Heidelberg 3084, Victoria, Australia.

Numan Kutaiba (N)

Department of Radiology, Austin Health, Heidelberg 3084, Victoria, Australia.

Samuel Hui (S)

Department of Gastroenterology, Austin Health, Heidelberg 3084, Victoria, Australia.
Department of Gastroenterology, Monash Health, Clayton 3168, Victoria, Australia.

Paul Gow (P)

Department of Gastroenterology, Austin Health, Heidelberg 3084, Victoria, Australia.
Victorian Liver Transplant Unit, Austin Health, Heidelberg 3084, Victoria, Australia.

Vijayaragavan Muralidharan (V)

Department of Surgery, University of Melbourne, Austin Health, Heidelberg 3048, Victoria, Australia.

Alexander Dobrovic (A)

Department of Surgery, Beacon Laboratory, Austin Precinct, The University of Melbourne, Austin Hospital, Heidelberg 3048, Victoria, Australia.

Adam Testro (A)

Department of Gastroenterology, Austin Health, Heidelberg 3084, Victoria, Australia.
Victorian Liver Transplant Unit, Austin Health, Heidelberg 3084, Victoria, Australia.

Classifications MeSH