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Clinical Trials in Germany / NCT06717919
Recruiting Phase 4

HOPE Against Cancer Recurrence in HCC

NCT06717919 · tracked via the Priya Life Science Germany tracker
Sponsor
Philipp Dutkowski
Phase
Phase 4
Started
2025-08-01
Last updated
2025-12-16

Condition(s) studied

Liver TransplantationHCCOncological Outcomes

Investigational drug(s) / intervention(s)

Hypothermic oxygenated perfusionConventional cold storage

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.

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.

Study 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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * 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 Exclusion Criteria: * Donation after circulatory death (DCD) liver grafts * Combined liver transplants * Partial liver transplants * Combined or mixed hepatocellular cholangiocarcinoma (cHCC-CCC) or pure cholangiocarcinoma or other malignancies in histopathology of the liver explant * Systemic antitumoural medical treatment with checkpoint inhibitors or multikinase inhibitors * Post-transplant treatment with mTOR inhibitors * Acute and unexpected medical contraindications * Pregnancy * Cold storage time of \> 10 hours (both study arms)

Primary outcome measure(s)

Trial sites (37)

FacilityCityRegionStatus
Rutgers New Jersey Medical School (New York) New York New York Not Yet Recruiting
Cleveland Clinic Cleveland Ohio Not Yet Recruiting
Medical University of Innsbruck Innsbruck Austria Recruiting
Medical University of Vienna Vienna Austria Recruiting
University Hospitals Leuven Leuven Belgium Recruiting
Institut de Recherche Expérimentale et Clinique (IREC) UCLouvain (Brussels) Woluwe-Saint-Lambert Belgium Recruiting
Institute for Clinical and Experimental Medicine (IKEM) (Prague) Prague Czechia Recruiting
Copenhagen University Hospital Copenhagen Denmark Recruiting
Hôpital de la Croix-Rousse (Lyon) Lyon France Not Yet Recruiting
Universitätsklinikum Essen Essen Germany Not Yet Recruiting
University Medical Centre Hamburg-Eppendorf Hamburg-Eppendorf Germany Not Yet Recruiting
Hannover Medical School Hanover Germany Not Yet Recruiting
University of Heidelberg Heidelberg Germany Not Yet Recruiting
University of Mainz Mainz Germany Not Yet Recruiting
University of Munich Grosshadern München Germany Not Yet Recruiting
Milano Institutio Nazionale dei Tumori (Milan) Milan Italy Not Yet Recruiting
ASST Grande Ospedale Metropolitano Niguarda (Milan) Milan Italy Not Yet Recruiting
Padova University Hospital Padova Italy Not Yet Recruiting
Gemelli University Hospital Rome Italy Not Yet Recruiting
University of Udine Udine Italy Recruiting
Lithuanian University of Health Sciences Kaunas Lithuania Not Yet Recruiting
University of Groningen and University Medical Centre Groningen Groningen Netherlands Not Yet Recruiting
University Medical Centre Rotterdam - Erasmus University Medical Center Rotterdam Netherlands Not Yet Recruiting
Oslo University Hospital Oslo Norway Not Yet Recruiting
Department of Surgical Oncology, Transplant Surgery and General Surgery, Medical University of Gdańsk Gdansk Poland Recruiting
Medical University of Warsaw Warsaw Poland Not Yet Recruiting
Centro Hepato-Bilio-Pancreático e de Transplantação (CHBPT) Lisbon Portugal Not Yet Recruiting
Vall d'Hebron Barcelona Hospital Campus Barcelona Spain Not Yet Recruiting
Karolinska Institutet (Stockholm) Stockholm Sweden Recruiting
Clarunis - University Digestive Health Care Basel Canton of Basel-City Not Yet Recruiting
University Hospital Zurich Zurich Canton of Zurich Not Yet Recruiting
Hôpitaux universitaires de Genève Geneva Switzerland Recruiting
University Hospitals Birmingham Birmingham United Kingdom Not Yet Recruiting
Leeds Teaching Hospitals NHS Trust Leeds United Kingdom Not Yet Recruiting
The Royal Free Hospital (London) London United Kingdom Not Yet Recruiting
King's College Hospital (London) London United Kingdom Not Yet Recruiting
Freeman Hospital (Newcastle) Newcastle United Kingdom Not Yet Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06717919 on ClinicalTrials.gov ↗ ← All trials in Germany