Hypothermic Oxygenated Perfusion (HOPE) Against Cancer Recurrence in HCC Liver Transplantation - International Multicentre Parallel Group Interventional RCT

Status: Recruiting
Location: See all (36) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

Liver transplantation is often performed to treat liver cancer, or hepatocellular carcinoma (HCC), in patients with impaired liver function due to cirrhosis. A shortcoming, however, is tumor recurrence after transplantation. Approximately 15 % of patients receiving livers develop recurrence and this depends on the quality of the liver received. Machine liver perfusion, for example, hypothermic oxygenated liver perfusion (HOPE), which means that the organ is perfused with an oxygen-rich fluid in a cold environment before transplantation, is a novel method to improve the quality of livers before implantation. The standard of care is cold storage without perfusion. The objective of this study is to compare the survival after tumor recurrence of patients after liver transplantation for HCC between perfused and not perfused livers. This study's hypothesis is that survival without tumor recurrence is improved when the liver is perfused before implantation. The study involves transplant centers worldwide, and adults with HCC waiting for liver transplantation are included. 220 Patients will be recruited within 12 months and then observed for at least 2 years after transplantation. To provide the most valid results, the patients will be randomly allocated to either the organ perfusion group or a control group with standard-of-care cold storage of the organ.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adult recipients (\>18y), listed for liver transplantation with documented HCC (Liver Imaging Reporting and Data System (LIRADS) 5 lesion in magnetic resonance imaging or computer tomography of the liver or biopsy proven),

• within up to seven criteria, i.e. HCC with seven as the sum of the diameter of the largest tumour (in cm) and the number of tumours at the time point of liver transplantation,

• written informed consent for the trial. This also includes patients beyond the up to seven criteria after successful downsizing of the HCC

Locations
United States
New York
Rutgers New Jersey Medical School (New York)
NOT_YET_RECRUITING
New York
Ohio
Cleveland Clinic
NOT_YET_RECRUITING
Cleveland
Other Locations
Austria
Medical University of Innsbruck
RECRUITING
Innsbruck
Medical University of Vienna
RECRUITING
Vienna
Belgium
University Hospitals Leuven
RECRUITING
Leuven
Institut de Recherche Expérimentale et Clinique (IREC) UCLouvain (Brussels)
RECRUITING
Woluwe-saint-lambert
Denmark
Copenhagen University Hospital
RECRUITING
Copenhagen
France
Hôpital de la Croix-Rousse (Lyon)
NOT_YET_RECRUITING
Lyon
Germany
Universitätsklinikum Essen
NOT_YET_RECRUITING
Essen
University Medical Centre Hamburg-Eppendorf
NOT_YET_RECRUITING
Hamburg-eppendorf
Hannover Medical School
NOT_YET_RECRUITING
Hanover
University of Heidelberg
NOT_YET_RECRUITING
Heidelberg
University of Mainz
NOT_YET_RECRUITING
Mainz
University of Munich Grosshadern
NOT_YET_RECRUITING
München
Italy
ASST Grande Ospedale Metropolitano Niguarda (Milan)
NOT_YET_RECRUITING
Milan
Milano Institutio Nazionale dei Tumori (Milan)
NOT_YET_RECRUITING
Milan
Padova University Hospital
NOT_YET_RECRUITING
Padua
Gemelli University Hospital
NOT_YET_RECRUITING
Rome
University of Udine
RECRUITING
Udine
Lithuania
Lithuanian University of Health Sciences
NOT_YET_RECRUITING
Kaunas
Netherlands
University of Groningen and University Medical Centre Groningen
NOT_YET_RECRUITING
Groningen
University Medical Centre Rotterdam - Erasmus University Medical Center
NOT_YET_RECRUITING
Rotterdam
Norway
Oslo University Hospital
NOT_YET_RECRUITING
Oslo
Poland
Department of Surgical Oncology, Transplant Surgery and General Surgery, Medical University of Gdańsk
RECRUITING
Gdansk
Medical University of Warsaw
NOT_YET_RECRUITING
Warsaw
Portugal
Centro Hepato-Bilio-Pancreático e de Transplantação (CHBPT)
NOT_YET_RECRUITING
Lisbon
Spain
Vall d'Hebron Barcelona Hospital Campus
NOT_YET_RECRUITING
Barcelona
Sweden
Karolinska Institutet (Stockholm)
RECRUITING
Stockholm
Switzerland
Clarunis - University Digestive Health Care
NOT_YET_RECRUITING
Basel
Hôpitaux universitaires de Genève
RECRUITING
Geneva
University Hospital Zurich
NOT_YET_RECRUITING
Zurich
United Kingdom
University Hospitals Birmingham
NOT_YET_RECRUITING
Birmingham
Leeds Teaching Hospitals NHS Trust
NOT_YET_RECRUITING
Leeds
King's College Hospital (London)
NOT_YET_RECRUITING
London
The Royal Free Hospital (London)
NOT_YET_RECRUITING
London
Freeman Hospital (Newcastle)
NOT_YET_RECRUITING
Newcastle
Contact Information
Primary
Philipp Dutkowski, Professor
philipp.dutkowski@clarunis.ch
0041 61 777 73 06
Time Frame
Start Date: 2025-08-01
Estimated Completion Date: 2028-01-31
Participants
Target number of participants: 220
Treatments
Active_comparator: Conventional cold storage
Conventional cold storage at 4°C will be performed with precooled preservation solution according to local standard of care. For cold storage at the Swiss centres, IGL-1 (Institute George Lopez) is used for cold storage. Liver transplant centres in other European countries, use mainly three other storage solutions (Histidine trypophan-ketoglutarat, HTK and University of Wisconsin, UW solution, Celsior) in accordance to their national guidelines.
Experimental: Hypothermic oxygenated perfusion
All study centres will use either VitaSmart, Liver assist or Perlife devices for machine liver perfusion, with a pressure controlled hypothermic oxygenated liver perfusion through the portal vein (HOPE) or through the portal vein and the hepatic artery (DHOPE), targeting a flow rate between 200-250 ml/min at a pressure of 3 mmHg, and a perfusate temperature between 8-12°C. The perfusate consists of 3L re-circulating Belzer MPS® (Bridge to Life Ltd.) with an active oxygenation (70-110 kPa). The minimum perfusion duration is defined at 2 hours, while perfusion is generally continued until the recipient hepatectomy is completed. The perfusion will exclusively be performed in the recipient centre after initial cold storage and bench preparation of the liver for implantation.~The perfusion devices are routinely used in all participating centres (VitaSmart, Bridge to Life®, Liver Assist, XVIVO®, Perlife, Aferitica®).
Sponsors
Leads: Philipp Dutkowski

This content was sourced from clinicaltrials.gov

Similar Clinical Trials