Actively Recruiting
An Innovative CFD-based Dosimetry and Pre-treatment Planning Platform to Support Personalized Transarterial Therapies for Liver Cancer
Led by University Hospital, Ghent · Updated on 2026-01-02
80
Participants Needed
1
Research Sites
275 weeks
Total Duration
On this page
Sponsors
U
University Hospital, Ghent
Lead Sponsor
U
University Ghent
Collaborating Sponsor
AI-Summary
What this Trial Is About
Transarterial radioembolization (TARE) is a key treatment option for patients with unresectable hepatocellular carcinoma (HCC), a primary form of liver cancer. TARE is a minimally invasive therapy in which radioactive microspheres are delivered through a microcatheter near the tumour into the liver's blood vessels. Although TARE can significantly improve survival, treatment outcomes remain variable and difficult to predict, mainly because of complex liver vasculature and unpredictable distribution of radioactive microspheres due to uncertain parameters such as catheter tip location, catheter orientation, and injection velocity. The long-term goal would be to make these treatments more predictable and effective by developing a patient-specific pre-treatment planning platform. Blood flow and microsphere transport will be modelled in a digital model of the patient-specific hepatic arterial tree (based on clinical imaging) using computational fluid dynamics (CFD), in combination with Monte Carlo-based radiation dosimetry. Using CFD simulations, we will investigate how variations in treatment parameters influence the microsphere distribution, aiming to better understand their role in treatment variability. This will allow us to predict the dose distribution of a certain treatment and determine potentially a more optimal set of treatment parameters. This research contributes to the broader field of cancer research by laying the foundations for a digital tool for personalized pre-treatment planning. The insights gained could support interventional radiologists in optimizing treatment planning, improving tumor targeting, and minimizing radiation exposure to healthy liver tissue in future TARE procedures.
CONDITIONS
Official Title
An Innovative CFD-based Dosimetry and Pre-treatment Planning Platform to Support Personalized Transarterial Therapies for Liver Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Radiologically diagnosed with hepatocellular carcinoma (HCC) and eligible for or undergoing treatment
- Treated or planned to be treated with transarterial radioembolization (TARE) using radioactive microspheres
- Have pre-treatment medical imaging of hepatic arterial vasculature (e.g., CT, MRI, PET, SPECT, DSA) suitable for 3D model development
You will not qualify if you...
- Undergoing TARE without adequate medical imaging of the hepatic vasculature
- No available pre- or post-treatment imaging data for analysis
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University Hospital Ghent
Ghent, Belgium, 9000
Actively Recruiting
Research Team
E
Elisabeth Dhondt, Dr.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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