Recruiting

TARE for HCCHolmium-166 Radioembolization for Advanced Liver Cancer

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What is being collected

Data Collection

Collected from past medical records and data - Retrospective
Who is being recruted

Digestive System Diseases+3

+ Fibrosis

+ Liver Cirrhosis

Over 18 Years
+14 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: February 2025
See protocol details

Summary

Principal SponsorUniversitair Ziekenhuis Brussel
Study ContactHelena Degroote
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: February 1, 2025

Actual date on which the first participant was enrolled.

This study is about exploring the use of Holmium-166 (Ho-166) transarterial radioembolization (TARE), a type of radiation therapy, for treating patients with a form of liver cancer known as hepatocellular carcinoma (HCC). HCC is an aggressive cancer that often develops in people with liver cirrhosis, typically due to long-term viral hepatitis or a condition called metabolic dysfunction-associated fatty liver disease. As HCC advances, treatment options become limited, especially when the cancer has reached advanced stages. The study aims to understand if Ho-166 TARE can offer significant benefits in managing HCC, potentially improving care for those who are not eligible for surgery or liver transplantation. In this study, patients receive Ho-166 TARE treatment, which involves the delivery of tiny particles containing the radioactive isotope Holmium-166 directly to the tumor site through the liver's blood supply. This targeted approach aims to destroy the tumor while minimizing harm to the surrounding healthy liver tissue. The study looks back at the medical records of patients who received this treatment between January 2010 and December 2024. It examines factors like patient demographics, tumor characteristics, side effects of the treatment, and how well the therapy worked. The primary goals are to evaluate the effectiveness of Ho-166 TARE in terms of overall survival and tumor response rate, and to assess its safety compared to other treatment options.

Official TitleHolmium-166 Transarterial Radioembolization for the Treatment of Hepatocellular Carcinoma
NCT06873269
Principal SponsorUniversitair Ziekenhuis Brussel
Study ContactHelena Degroote
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

100 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Digestive System DiseasesFibrosisLiver CirrhosisLiver DiseasesPathologic ProcessesPathological Conditions, Signs and Symptoms

Criteria

7 inclusion criteria required to participate
aged 18 year or older

diagnosed with locally advanced HCC without extra-hepatic metastases

HCC must not be amendable to treatment by surgical resection or percutaneous radiofrequency ablation

after assessment by the investigator and multidisciplinary tumor board, the patient is considered suitable for protocol treatment with Holmium-166 TARE

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7 exclusion criteria prevent from participating
prior treatment with any of the following treatment modalities for HCC: systemic therapy, hepatic radiation therapy

currently enrolled in clinical studies where patient receive investigational therapeutic drug

metastatic disease

concurrent malignancy

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Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

UZ Brussel

Brussels, BelgiumOpen UZ Brussel in Google Maps
Recruiting
One Study Center