Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04351204

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Netherlands Cancer Institute

Amsterdam, Netherlands, 1066CX

Actively Recruiting

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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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