# HCC recurrence in liver transplants treated with hypothermic oxygenated machine perfusion: An international matched cohort study

**Authors:** Janina Eden, Philip C. Müller, Christoph Kuemmerli, Marco Bongini, Francesca Albanesi, Carlo Sposito, Gabriela Berlakovich, Bettina M. Buchholz, Florin Botea, Stefania Camagni, Matteo Cescon, Umberto Cillo, Fabio Colli, Philippe Compagnon, Luciano G. De Carlis, Riccardo De Carlis, Fabrizio Di Benedetto, Jule Dingfelder, Dulce Diogo, Daniele Dondossola, Moritz Drefs, Jiri Fronek, Giuliana Germinario, Enrico Gringeri, Christiano Guidetti, Georg Györi, Matej Kocik, Efrayim H. Küçükerbil, Dionysios Koliogiannis, Hwai-Ding Lam, Georg Lurje, Paolo Magistri, Diethard Monbaliu, Mostafa el Moumni, Beat P. Müller, Damiano Patrono, Wojciech G. Polak, Robert J. Porte, Matteo Ravaioli, Michel Rayar, Renato Romagnoli, Gustaf Sörensen, Deniz Uluk, Pierre A. Clavien, Vincenzo Mazzaferro, Philipp Dutkowski, Vincent E. de Meijer

PMC · DOI: 10.1016/j.jhepr.2026.101732 · JHEP Reports · 2026-01-21

## TL;DR

Hypothermic oxygenated machine perfusion (HOPE) treatment of liver grafts is linked to lower HCC recurrence and better survival in liver transplant recipients compared to non-perfused grafts.

## Contribution

First large international study showing HOPE reduces HCC recurrence and improves survival in liver transplants.

## Key findings

- HCC recurrence rate was 6.9% in HOPE-treated liver transplants.
- HOPE-treated HCC recipients had significantly better 5-year survival than non-perfused graft recipients.
- Survival in HOPE-treated HCC recipients was comparable to non-HCC recipients.

## Abstract

Liver transplantation (LT) for hepatocellular carcinoma (HCC) is performed worldwide, with 5-year survival rates of approximately 70%. However, post-transplant HCC recurrence occurs in 15-20% of recipients. We aimed to evaluate, for the first time, long-term recurrence-free survival in a large international cohort of patients undergoing LT for HCC using grafts treated with hypothermic oxygenated machine perfusion (HOPE).

This observational post hoc analysis of the multicenter European HOPE-REAL study (NCT05520320) included adult recipients with HCC (N = 599) who received a liver from either a donation after brain death (DBD) or donation after circulatory death (DCD) donor, preserved using HOPE, dual-HOPE (DHOPE), or normothermic regional perfusion followed by HOPE (NRP-HOPE) between 2012 and 2022. Propensity score matching was used to compare outcomes between HCC and non-HCC recipients within the HOPE-REAL cohort, and between HOPE-treated HCC recipients and an external control cohort receiving non-perfused livers (n = 484).

The overall HCC recurrence rate in the HOPE-REAL cohort was 6.9% (41/599), with no significant difference between DBD and DCD liver transplants (7.1% [25/350] vs. 6.4% [16/249]; p = 0.346). One-, 3-, and 5-year overall survival rates were 92%, 86%, and 81%, while recurrence-free survival rates were 90%, 83%, and 78%, respectively. Five-year overall survival was similar between 347 HOPE-treated HCC recipients (82%) and 347 matched non-HCC recipients (84%) (p = 0.625). In contrast, compared to an external cohort of 312 non-perfused HCC recipients, 5-year overall survival was significantly higher in 312 matched HOPE-treated HCC recipients (74% vs. 84%; p = 0.034).

HCC recurrence was rare after transplantation of livers treated with HOPE. Long-term survival in HOPE-treated HCC recipients was significantly better than in those receiving non-perfused livers, and comparable to outcomes in non-HCC recipients. These findings warrant validation in a randomized clinical trial.

This post hoc analysis of the HOPE REAL study demonstrates, for the first time, low hepatocellular carcinoma (HCC) recurrence rates in a large cohort of hypothermic oxygenated machine perfusion-treated liver transplant recipients with HCC, and significantly better survival outcomes compared to matched recipients of non-perfused grafts. These findings may have important implications, particularly as tumor-related indications for liver transplantation continue to rise. Machine liver perfusion could emerge as a novel strategy to improve oncological outcomes in high-risk cancer conditions after transplantation, potentially via mitigation of inflammation and reduced tumor cell seeding.

NCT05520320

Image 1

•HOPE treatment was identified as an independent significant protective factor against HCC recurrence.•Among patients with HCC, 5-year suvival and recurrence -free survival was higher in matched recipients of HOPE treated DBD grafts than non-perfused DBD grafts (84% vs. 74% and 77 vs. 67%, respectively).•In contrast, survival was not different between HOPE treated HCC recipients and matched non HCC recipients ( 82% vs 84% at 5 years).

HOPE treatment was identified as an independent significant protective factor against HCC recurrence.

Among patients with HCC, 5-year suvival and recurrence -free survival was higher in matched recipients of HOPE treated DBD grafts than non-perfused DBD grafts (84% vs. 74% and 77 vs. 67%, respectively).

In contrast, survival was not different between HOPE treated HCC recipients and matched non HCC recipients ( 82% vs 84% at 5 years).

## Linked entities

- **Diseases:** hepatocellular carcinoma (MONDO:0007256), HCC (MONDO:0007256)

## Full-text entities

- **Genes:** IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559] {aka CD25, IDDM10, IL2R, IMD41, TCGFR, p55}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, FOXP3 (forkhead box P3) [NCBI Gene 50943] {aka AIID, DIETER, IPEX, JM2, PIDX, XPID}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, DCD (dermcidin) [NCBI Gene 117159] {aka AIDD, DCD-1, DSEP, HCAP, PIF}, HMGB1 (high mobility group box 1) [NCBI Gene 3146] {aka HMG-1, HMG1, HMG3, SBP-1}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}
- **Diseases:** liver fibrosis (MESH:D008103), ischemic (MESH:D002545), Tumor (MESH:D009369), PD (MESH:D010300), mitochondrial dysfunction (MESH:D028361), circulatory (MESH:D012769), inflammation (MESH:D007249), HOPE (MESH:D000860), ischemia (MESH:D007511), mitochondrial complex I dysfunction (MESH:C537475), DBD (MESH:D001926), hypoxic (MESH:D002534), death (MESH:D003643), IRI (MESH:D015427), MELD (MESH:D058625), metastases (MESH:D009362), HCC (MESH:D006528), necrosis (MESH:D009336), liver damage (MESH:D056486)
- **Chemicals:** succinate (MESH:D019802), DHOPE (-), reactive oxygen species (MESH:D017382), NADH (MESH:D009243), ATP (MESH:D000255)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12926642/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926642/full.md

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Source: https://tomesphere.com/paper/PMC12926642