Actively Recruiting
The MR-Linac Technical Feasibility Protocol
Led by The Netherlands Cancer Institute · Updated on 2024-02-01
140
Participants Needed
1
Research Sites
388 weeks
Total Duration
On this page
Sponsors
T
The Netherlands Cancer Institute
Lead Sponsor
E
Elekta Limited
Collaborating Sponsor
AI-Summary
What this Trial Is About
Radiation therapy is predominantly based on a Computed Tomography (CT) scan obtained during the treatment planning phase. During the course of radiotherapy, however, both the tumor and organs at risk (OAR) are variable in position, shape and size between fractions, and during beam delivery within one treatment fraction. Around the clinical target volume (CTV) a safety margin (Planning Target Volume, PTV) is created to account for these geometric uncertainties to ensure that the tumor receives the prescribed dose. Direct integration of imaging at the linear accelerator enables daily monitoring of patient positioning, tumor position, and alterations in patient anatomy. Image guided radiotherapy (IGRT) enables the detection and immediate correction of such deviations and increases the precision of delivery. Adaptive radiotherapy has become an important strategy for serially modifying dose distributions in a manner that can substantially reduce OAR dose and subsequent toxicity, while maintaining adequate target coverage. Current adaptive protocols rely upon a standard CT-based workflow and (cone-beam) CT-based image guidance. Magnetic Resonance Imaging (MRI) has superior soft-tissue contrast over CT and seems a very promising modality to integrate in the radiation treatment process, facilitating better visualization of the tumor and OAR during treatment.
CONDITIONS
Official Title
The MR-Linac Technical Feasibility Protocol
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient age 18 years or older treated with radiation therapy on the MR-Linac
- WHO performance status between 0 and 2
- Ability to understand and willingness to sign a written informed consent document
You will not qualify if you...
- Contraindications for MRI examination
- Pregnancy
- Claustrophobia
- Weight over 140 kg and/or body width over 60 cm
- Any other significant medical condition or severe psychiatric illness/social situation that may interfere with study participation or compliance, as judged by the treating physician
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Netherlands Cancer Institute
Amsterdam, Netherlands, 1066CX
Actively Recruiting
Research Team
M
Marlies Nowee, MD, PhD
CONTACT
U
Uulke vd Heide, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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