End-ischemic Hypothermic Oxygenated Perfusion for Extended Criteria Donors in Liver Transplantation – A multicenter, randomized controlled trial - HOPExt

Author:

Pradat Pierre1ORCID,Pantel Solène2,Maynard Marianne3,Lalande Laure4,Thevenon Sylvie2,Adam René5,Allard Marc-Antoine <5,Robin Fabien6,Rayar Michel6,BOLESLAWSKI Emmanuel7,Scatton Olivier8,Chirica Mircea9,Faitot François10,Bachellier Philippe10,Soubrane Olivier11,Mohkam Kayvan12,Mabrut Jean-Yves12,Lesurtel Mickaël12

Affiliation:

1. Hospices Civils de Lyon

2. Hospices Civils de Lyon, Croix-Rousse Hospital, Centre for Clinical Research

3. Hospices Civils de Lyon, Croix Rousse Hospital, Centre for Clinical Research

4. Hospices Civils de Lyon, Croix-Rousse Hospital, Department of Pharmacy

5. Paul Brousse University Hospital, Department of HPB surgery and liver transplantation

6. Pontchaillou University Hospital

7. Claude Huriez University Hospital

8. Hospital Pitie-Salpetriere: Hopital Universitaire Pitie Salpetriere

9. Hospital Michallon: Centre Hospitalier Universitaire Grenoble Alpes Hopital Michallon

10. Hautepierre University Hospital

11. Beaujon University Hospital

12. Hospices Civils de Lyon, Croix-Rousse Hospital

Abstract

Abstract Background: Given the scarce donor supply, an increasing number of so-called marginal or extended criteria donor (ECD) organs are used for liver transplantation. These ECD liver grafts are however known to be associated with a higher rate of early allograft dysfunction and primary non-function because of a greater vulnerability to ischemia-reperfusion injury. The end-ischemic Hypothermic Oxygenated Machine Perfusion (HOPE) technique may improve outcomes of liver transplantation with ECD grafts by decreasing reperfusion injury. Methods: HOPExt trial is a comparative open-label, multicenter, national, prospective, randomized, controlled study, in two parallel groups, using static cold storage, the gold standard procedure, as control. The trial will enroll adult patients on the transplant waiting list for liver failure or liver cirrhosis and/or liver malignancy requiring liver transplantation and receiving an ECD liver graft from a brain-dead donor. In the experimental group, ECD liver grafts will first undergo a classical static cold (4°C) storage followed by a hypothermic oxygenated perfusion (HOPE) for a period of 1 to 4 hours. The control group will consist of the classic static cold storage which is the gold standard procedure in liver transplantation. The primary objective of this trial is to study the efficacy of HOPE used before transplantation of ECD liver grafts from brain-dead donors in reducing postoperative early allograft dysfunction within the first 7 postoperative days compared to simple cold static storage. Discussion: We present in this protocol all study procedures in regard to the achievement of the HOPExt trial, to prevent biased analysis of trial outcomes and improve the transparency of the trial results. Enrollment of patients in the HOPExt trial has started on June 31, 2021, and is ongoing Trial registration: ClinicalTrials.gov NCT03929523. Registered on April 29, 2019, before the start of inclusion.

Publisher

Research Square Platform LLC

Reference24 articles.

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2. Gracia-Sancho J, Casillas-Ramírez A, Peralta C. Molecular pathways in protecting the liver from ischaemia/reperfusion injury: a 2015 update. Clin Sci. 2015 Aug 1;129(4):345–62.

3. Waitlist Mortality Decreases with Increased Use of Extended Criteria Donor Liver Grafts at Adult Liver Transplant Centers;Barshes NR;Am J Transplant

4. Howard TK, Klintmalm GBG, Cofer JB, Husberg BS, Goldstein RM, Gonwa TA, THE INFLUENCE OF PRESERVATION INJURY ON REJECTION IN THE HEPATIC TRANSPLANT RECIPIENT. :Transplantation. 1990 Jan;49(1):103–6.

5. Croome KP, Hernandez-Alejandro R, Chandok N. Early Allograft Dysfunction Is Associated With Excess Resource Utilization After Liver Transplantation. Transplant Proc. 2013 Jan;45(1):259–64.

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