Breast Cancer, Esophageal Cancer, Head and Neck Cancer, Liver Cancer, Oligometastasis, Prostate Cancer, Rectal Cancer
Conditions
Keywords
Radiotherapy, Adaptive Radiotherapy
Brief summary
This study investigates the feasibility of imaging and treatment on a novel 1.5 T MR-Linac radiotherapy hybrid device.
Detailed description
Novel hybrid devices combine magnetic resonance imaging (MRI) and a linear accelerator in a single device. The superior soft tissue contrast compared with cone-beam computed tomography based treatment and the possibility for daily plan adaptation promise a higher precision of treatment, better target volume coverage and normal tissue sparing. In a first step the present study will test the feasibility of imaging and treatment on the 1.5 T MR-Linac.
Interventions
Radiotherapy is performed on the 1.5 T MR Linac
Only imaging performed on the MR Linac
Sponsors
Study design
Eligibility
Inclusion criteria
* existing indication for radiation therapy * minimum age 18 years, no upper age limit * capacity for consent * Informed consent
Exclusion criteria
* contraindication for MRI (claustrophobia, metallic implants not applicable for MRI * pregnancy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Feasibility of online MR guided Radiotherapy | During every single patients treatment (i.e. between one to seven weeks after the first application of radiotherapy) | Treatment of a patient is considered feasible when 85% of treatments were completed as planned in this patient |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Time analysis | During every single patients treatment (i.e. between one to seven weeks after the first application of radiotherapy) | Time required for online MR guided radiotherapy |
Countries
Germany