TY - JOUR
T1 - Long-term outcomes after hypothermic oxygenated machine perfusion and transplantation of 1,202 donor livers in a real-world setting (HOPE-REAL study)
AU - Eden, Janina
AU - Brüggenwirth, Isabel M.A.
AU - Berlakovich, Gabriela
AU - Buchholz, Bettina M.
AU - Botea, Florin
AU - Camagni, Stefania
AU - Cescon, Matteo
AU - Cillo, Umberto
AU - Colli, Fabio
AU - Compagnon, Philippe
AU - De Carlis, Luciano G.
AU - De Carlis, Riccardo
AU - Di Benedetto, Fabrizio
AU - Dingfelder, Jule
AU - Diogo, Dulce
AU - Dondossola, Daniele
AU - Drefs, Moritz
AU - Fronek, Jiri
AU - Germinario, Giuliana
AU - Gringeri, Enrico
AU - Györi, Georg
AU - Kocik, Matej
AU - Küçükerbil, Efrayim H.
AU - Koliogiannis, Dionysios
AU - Lam, Hwai Ding
AU - Lurje, Georg
AU - Magistri, Paolo
AU - Monbaliu, Diethard
AU - Moumni, Mostafa el
AU - Patrono, Damiano
AU - Polak, Wojciech G.
AU - Ravaioli, Matteo
AU - Rayar, Michel
AU - Romagnoli, Renato
AU - Sörensen, Gustaf
AU - Uluk, Deniz
AU - Schlegel, Andrea
AU - Porte, Robert J.
AU - Dutkowski, Philipp
AU - de Meijer, Vincent E.
N1 - Publisher Copyright: © 2024 The Author(s)
PY - 2025/1
Y1 - 2025/1
N2 - Background & Aims: Despite strong evidence for improved preservation of donor livers by machine perfusion, longer post-transplant follow-up data are urgently needed in an unselected patient population. We aimed to assess long-term outcomes after transplantation of hypothermic oxygenated machine perfusion (HOPE)-treated donor livers based on real-world data (i.e., IDEAL-D stage 4). Methods: In this international, multicentre, observational cohort study, we collected data from adult recipients of HOPE-treated livers transplanted between January 2012 and December 2021. Analyses were stratified by donation after brain death (DBD) and donation after circulatory death (DCD), sub-divided by their respective risk categories. The primary outcome was death-censored graft survival. Secondary outcomes included the incidence of primary non-function (PNF) and ischaemic cholangiopathy (IC). Results: We report on 1,202 liver transplantations (64% DBD) performed at 22 European centres. For DBD, a total number of 99 benchmark (8%), 176 standard (15%), and 493 extended-criteria (41%) cases were included. For DCD, 117 transplants were classified as low risk (10%), 186 as high risk (16%), and 131 as futile (11%), with significant risk profile variations among centres. Actuarial 1-, 3-, and 5-year death-censored graft survival rates for DBD and DCD livers were 95%, 92%, and 91%, vs. 92%, 87%, and 81%, respectively (log-rank p = 0.003). Within DBD and DCD strata, death-censored graft survival was similar among risk groups (log-rank p = 0.26, p = 0.99). Graft loss due to PNF or IC was 2.3% and 0.4% (DBD), and 5% and 4.1% (DCD). Conclusions: This study shows excellent 5-year survival after transplantation of HOPE-treated DBD and DCD livers with low rates of graft loss due to PNF or IC, irrespective of their individual risk profile. HOPE treatment has now reached IDEAL-D stage 4, which further supports its implementation in routine clinical practice. Trial registration: ClinicalTrials.gov Identifier: NCT05520320. Impact and implications: This study demonstrates the excellent long-term performance of hypothermic oxygenated machine perfusion (HOPE) treatment of donation after circulatory and donation after brain death liver grafts irrespective of their individual risk profile in a real-world setting, outside the evaluation of randomised-controlled trials. While previous studies have established safety, feasibility, and efficacy against the current standard, according to the IDEAL-D evaluation framework, HOPE treatment has now reached the final IDEAL-D stage 4, which further supports its implementation in routine clinical practice.
AB - Background & Aims: Despite strong evidence for improved preservation of donor livers by machine perfusion, longer post-transplant follow-up data are urgently needed in an unselected patient population. We aimed to assess long-term outcomes after transplantation of hypothermic oxygenated machine perfusion (HOPE)-treated donor livers based on real-world data (i.e., IDEAL-D stage 4). Methods: In this international, multicentre, observational cohort study, we collected data from adult recipients of HOPE-treated livers transplanted between January 2012 and December 2021. Analyses were stratified by donation after brain death (DBD) and donation after circulatory death (DCD), sub-divided by their respective risk categories. The primary outcome was death-censored graft survival. Secondary outcomes included the incidence of primary non-function (PNF) and ischaemic cholangiopathy (IC). Results: We report on 1,202 liver transplantations (64% DBD) performed at 22 European centres. For DBD, a total number of 99 benchmark (8%), 176 standard (15%), and 493 extended-criteria (41%) cases were included. For DCD, 117 transplants were classified as low risk (10%), 186 as high risk (16%), and 131 as futile (11%), with significant risk profile variations among centres. Actuarial 1-, 3-, and 5-year death-censored graft survival rates for DBD and DCD livers were 95%, 92%, and 91%, vs. 92%, 87%, and 81%, respectively (log-rank p = 0.003). Within DBD and DCD strata, death-censored graft survival was similar among risk groups (log-rank p = 0.26, p = 0.99). Graft loss due to PNF or IC was 2.3% and 0.4% (DBD), and 5% and 4.1% (DCD). Conclusions: This study shows excellent 5-year survival after transplantation of HOPE-treated DBD and DCD livers with low rates of graft loss due to PNF or IC, irrespective of their individual risk profile. HOPE treatment has now reached IDEAL-D stage 4, which further supports its implementation in routine clinical practice. Trial registration: ClinicalTrials.gov Identifier: NCT05520320. Impact and implications: This study demonstrates the excellent long-term performance of hypothermic oxygenated machine perfusion (HOPE) treatment of donation after circulatory and donation after brain death liver grafts irrespective of their individual risk profile in a real-world setting, outside the evaluation of randomised-controlled trials. While previous studies have established safety, feasibility, and efficacy against the current standard, according to the IDEAL-D evaluation framework, HOPE treatment has now reached the final IDEAL-D stage 4, which further supports its implementation in routine clinical practice.
UR - http://www.scopus.com/inward/record.url?scp=85200925702&partnerID=8YFLogxK
U2 - 10.1016/j.jhep.2024.06.035
DO - 10.1016/j.jhep.2024.06.035
M3 - Article
C2 - 38969242
AN - SCOPUS:85200925702
SN - 0168-8278
VL - 82
SP - 97
EP - 106
JO - Journal of Hepatology
JF - Journal of Hepatology
IS - 1
ER -