RealMove (Lung): Assessing Tumour Motion With Dynamic MRI
Region Stockholm
150 participants
Mar 15, 2024
INTERVENTIONAL
Conditions
Summary
The study aims to develop an improved method to tailor the geometric safety margin when treating with stereotactic body radiotherapy (SBRT), to avoid tumour cells being missed during irradiation and to limit the exposure of normal tissues as much as possible. Dynamic magnetic resonance imaging (MRI) is assumed to represent the tumour motion during the respiratory cycle more realistically, compared to 4-dimensional computed tomography (4D CT), thanks to its high temporal resolution and the possibility to image the motion over a longer period of time. Patients receiving SBRT for a pulmonary target located below the level of the carina are included in the study, and the hypothesis will be tested through a comparison of the tumour amplitude measured with each modality. Furthermore, the predictive value of the image series acquired at treatment planning, for the motion patterns observed at each treatment fraction, will be evaluated through repeated 4D CBCT acquisitions.
Eligibility
Inclusion Criteria4
- Accepted for SBRT treatment of one or more caudally situated lung targets (NSCLC or metastases), i.e. below the carina.
- Age ≥ 18 years
- Adequate clinical condition to maintain immobilised position for at least 30 minutes
- Adequate Swedish skills and cognitive function to understand study information and to fill in the questionnaire
Exclusion Criteria3
- Pregnancy or breastfeeding, or planned pregnancy or breastfeeding, during treatment
- Contraindication for MRI examination
- Otherwise incapable of participating in study
Interventions
Subjects receive a study-specific dynamic MRI scan. If the hypothesis of the study is confirmed, this examination can be used to inform future patients' treatment planning, replacing the use of 4D CT.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06322329