Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Jun 26:37:12781.
doi: 10.3389/ti.2024.12781. eCollection 2024.

Transjugular Intrahepatic Portosystemic Shunt Is Associated With Better Waitlist Management of Liver Transplant Candidates With Hepatocellular Carcinoma

Affiliations

Transjugular Intrahepatic Portosystemic Shunt Is Associated With Better Waitlist Management of Liver Transplant Candidates With Hepatocellular Carcinoma

Sofia El Hajji et al. Transpl Int. .

Abstract

Transjugular intrahepatic portosystemic shunt (TIPS) reduces portal hypertension complications. Its impact on hepatocellular carcinoma (HCC) remains unclear. We evaluated 42,843 liver transplant candidates with HCC from the Scientific Registry of Transplant Recipients (2002-2022). 4,484 patients with and without TIPS were propensity score-matched 1:3. Analysing wait-list changes in total tumor volume, HCC count, and alpha-fetoprotein levels, and assessing survival from listing and transplantation; TIPS correlated with a decreased nodule count (-0.24 vs. 0.04, p = 0.028) over a median wait period of 284 days (IQR 195-493) and better overall survival from listing (95.6% vs. 91.5% at 1 year, p < 0.0001). It was not associated with changes in tumor volume (0.28 vs. 0.11 cm³/month, p = 0.58) and AFP (14.37 vs. 20.67 ng/mL, p = 0.42). Post-transplant survival rates (91.8% vs. 91.7% at 1 year, p = 0.25) and HCC recurrence (5.1% vs. 5.9% at 5 years, p = 0.14) were similar, with a median follow-up of 4.98 years (IQR 2.5-8.08). While TIPS was associated with a reduced nodule count and improved waitlist survival, it did not significantly impact HCC growth or aggressiveness. These findings suggest potential benefits of TIPS in HCC management, but further studies need to confirm TIPS safety.

Keywords: hepatocellular carcinoma; liver transplantation; progression; recurrence; survival.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

None
Created with Biorender.com.
FIGURE 1
FIGURE 1
Overall survival from listing in the matched cohort, censoring transplanted patients and comparing patients with and without TIPS.
FIGURE 2
FIGURE 2
Overall survival from transplantation in the matched cohort comparing patient with and without TIPS.
FIGURE 3
FIGURE 3
Competed cumulative risk incidence of HCC recurrence comparing patients with and without TIPS. Gray’s test p = 0.14.

Similar articles

Cited by

References

    1. García-Pagán JC, Saffo S, Mandorfer M, Garcia-Tsao G. Where Does TIPS Fit in the Management of Patients with Cirrhosis? JHEPReport (2020) 2(4):100122. 10.1016/j.jhepr.2020.100122 - DOI - PMC - PubMed
    1. Franchis Rde, Bosch J, Garcia-Tsao G, Reiberger T, Ripoll C, Abraldes JG, et al. Baveno VII – Renewing Consensus in portal Hypertension. J Hepatol (2022) 76(4):959–74. 10.1016/j.jhep.2021.12.022 - DOI - PMC - PubMed
    1. Thabut D, Kudo M. Treatment of portal Hypertension in Patients with HCC in the Era of Baveno VII. J Hepatol (2023) 78(3):658–62. 10.1016/j.jhep.2022.11.019 - DOI - PubMed
    1. Allaire M, Rudler M, Thabut D. Portal Hypertension and Hepatocellular Carcinoma: Des Liaisons Dangereuses. Liver Int (2021) 41(8):1734–43. 10.1111/liv.14977 - DOI - PubMed
    1. Hüsing-Kabar A, Meister T, Köhler M, Domschke W, Kabar I, Wilms C, et al. Is De Novo Hepatocellular Carcinoma after Transjugular Intrahepatic Portosystemic Shunt Increased? United Eur Gastroenterol J (2018) 6(3):413–21. 10.1177/2050640617732886 - DOI - PMC - PubMed

MeSH terms

Substances

LinkOut - more resources