Evaluating the role of PET/CT scans in liver transplant candidates with liver cancer
Official title: Extension of Liver Transplantation Opportunity to Patients Suffering From Milan-out, Up-to-7-in, Hepatocellular Carcinoma: a Prospective Belgian Study of the Value of Negative 18FDG PET/CT
Run by University of Liege · NCT05276037 · Data updated 2026-11-12
This study is trying to see if PET/CT scans can help doctors choose the best liver cancer patients for liver transplants to improve their chances of survival.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 80 Years |
| Sex | All |
| Enrollment | 350 (estimated) |
| Sponsor | University of Liege Academic / other |
| Locations | 6 sites (Antwerp and 5 other locations) |
| Status | Recruiting |
| Started | January 1, 2019 |
| Main results expected | January 1, 2025 |
| Study ends | January 1, 2029 |
| Registry record updated | September 1, 2022 |
| Trial ID | NCT05276037 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults aged 18 to 80 with hepatocellular carcinoma who are being considered for liver transplantation.
✕Probably not a fit
Patients under 18 or over 80 years old, or those with contraindications for liver transplantation due to medical or cancer-related issues, will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to assess the prognostic value of negative 18FDG PET/CT scans in patients with hepatocellular carcinoma (HCC) who are candidates for liver transplantation. It will include adult patients aged 18 to 80 years who are discussed for potential liver transplantation at six Belgian centers. The study will create a secured, anonymized database to track patient outcomes and determine the effectiveness of using PET/CT imaging in selecting candidates based on the Milan criteria. The goal is to improve patient selection for liver transplantation and ultimately enhance survival rates.
Why it matters
Potential benefit: If successful, this study could improve the selection process for liver transplantation, leading to better outcomes for patients with hepatocellular carcinoma.
How similar studies have gone: Other studies have shown promising results using imaging techniques like PET/CT in similar contexts, suggesting that this approach may be beneficial.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * HepatoCellular Carcinoma * Liver transplant candidate after multidisciplinary disccuss Exclusion Criteria: * Patients \< 18y or \> 80yr old * Patients considered contra-indicated (CI) for LT due to non-liver-related medical problems (age, other cancer, psychiatric disease, uncontrolled infection, no compliance, active alcohol abuse, cardiac CI, pulmonary CI, surgical CI, other medical CI); * Patients contra-indicated for LT due to the HCC: extra-hepatic metastases (M+), lymphatic involvement (N+), macro-vascular invasion.
Where it's running
-
University Hospital, Antwerp
Antwerp, Belgium Recruiting -
Free University of Brussels
Brussels, Belgium Recruiting -
University Hospital, Ghent
Ghent, Belgium Recruiting -
Catholic University of Louvain
Leuven, Belgium Recruiting -
Leuven University hospital
Leuven, Belgium Recruiting -
ULiège
Liège, Belgium Recruiting
Study contacts
- Study coordinator: Olivier Detry, MD PhD
- Email: olivier.detry@chuliege.be
- Phone: 003242844757
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
InstaSure Non-Invasive Finger-Press Test for HCC
This study tests a non-invasive finger-skin test to help identify hepatocellular carcinoma in adults.
-
BGB-B2033 vs Sorafenib or Lenvatinib for advanced liver cancer
This study tests whether the investigational drug BGB-B2033 can help people with advanced hepatocellular carcinoma when given after prior PD-1/PD-L1 therapy, compared with the standard medicines sorafenib or lenvatinib.
-
Zinc add-on with targeted therapy plus immunotherapy for advanced liver cancer
This study tests whether adding daily zinc to standard targeted therapy and immunotherapy helps people with unresectable or advanced hepatocellular carcinoma.
-
68Ga-SorB PET/CT imaging for solid tumors
This study tests a new PET tracer called 68Ga-SorB to see if it can safely and accurately detect tumors in adults with melanoma, liver, lung, breast, pancreatic, ovarian cancer, or cholangiocarcinoma.
-
Hepatocellular Carcinoma Patient Registry (CHARM Hepatocellular Carcinoma MEA)
This observational study collects medical records of adults with hepatocellular carcinoma to understand how the disease presents and progresses across regions in the Middle East and North Africa.
-
GLP-1 RA plus standard treatment in first-line metastatic GI cancers
This early-phase trial tests whether adding a GLP-1 receptor agonist to standard first-line chemotherapy is safe and feasible for people with metastatic pancreatic, colorectal, or liver cancer.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.