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Clinical Trials in the Netherlands / NCT06768242
Starting soon Not applicable

Part of the Modern Art Study

NCT06768242 · tracked via the Priya Life Science Netherlands tracker
Phase
Not applicable
Started
2025-01
Last updated
2025-01-10

Condition(s) studied

HCC - Hepatocellular CarcinomaLiver Metastases

Investigational drug(s) / intervention(s)

Cone beam CT

Cone beam CT: Each patient will undergo three cone beam CTs per session, and a total of three sessions.

Study summary

One of the possible treatments for patients with liver tumours (hepatocellular carcinoma (HCC) or liver metastases) at the Erasmus MC is stereotactic body radiation therapy (SBRT) on the Cyberknife. To spare the organs at risk, suboptimal coverage of the planning target volume is sometimes accepted. The Ethos treatment system is equipped with a novel cone-beam CT (CBCT), which provides higher quality images. This makes it possible to consider online adaptive radiotherapy with daily plan adaptation, potentially leading to a higher dose on the tumour whilst sparing the surrounding healthy tissue more.

Liver tumours move with the breathing motion. On the CyberKnife, a tracking technology is used to keep track of the tumour, but this is not available on the Ethos. Because of this, breath holds will be used for breathing management, but appropriate safety margins need to be established under the new treatment conditions. The aim of this study is to determine the reproducibility of the tumour position for each breath hold within a treatment fraction, and also between treatment fractions, which is a crucial component in the establishment of appropriate safety margins.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Written informed consent; * Patient discussed in multidisciplinary tumor board; * Patient diagnosed with liver metastases and referred to the dept. of Radiotherapy for SBRT OR patient ≥65 years, diagnosed with HCC and referred to the dept. of Radiotherapy for SBRT; * Able to comply with breath-hold requirements. Exclusion Criteria: * Eligibility for surgery, ablation or liver transplantation.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Erasmus Medical Center Rotterdam South Holland

More Erasmus Medical Center trials in the Netherlands

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 NCT06768242 on ClinicalTrials.gov ↗ ← All trials in the Netherlands