Recipient organisationNIHR Manchester Biomedical Research Centre
NIHR supportRecorded as supported by this research centre
PeriodFeb 2025 — Jul 2028
In plain English
AI plain-English summary
A magnetic resonance imaging scanner and a radiotherapy machine have been combined into a single device—the MR Linac—and this study will test whether it can deliver precise, high-dose radiation to hard-to-see tumours in the abdomen and lung. Standard X-ray guided radiotherapy struggles to distinguish these tumours from surrounding healthy tissue, and the targets shift with breathing and digestion. The MR Linac’s superior imaging lets clinicians see the tumour in real time, adapt the radiation beam as the target moves, and potentially escalate the dose to the cancer while sparing normal organs. Current stereotactic ablative radiotherapy (SABR) already reduces treatment from 20-plus sessions to a handful, but its precision is limited by poor image quality and motion. This feasibility study will treat patients using published SABR prescriptions, then analyse the acquired images to explore safe dose escalation, real-time adaptation, and advanced imaging techniques such as diffusion-weighted and oxygen-enhanced MRI. If successful, the work could make SABR safer and more effective for liver, pancreas, kidney, and lung cancers—tumour sites where NHS England has already commissioned treatment but where precision remains a barrier. The findings would inform larger trials and, ultimately, clinical adoption of MR-guided radiotherapy.
View original technical description
This study aims to test the feasibility and suitability of the Magnetic Resonance Linear Accelerator (MR Linac) for the delivery of stereotactic ablative radiotherapy (SABR) for patients with cancers in the abdomen and lung. Over the past two decades SABR has been used increasingly for treatment of tumours of the liver, pancreas, kidney and lung. SABR delivers radiation in a high dose per fraction, usually on alternated days, that is precisely delivered, reducing the need for patients to attend 20+ treatments, whilst ablating the tumour or residual disease. NHS England has recently commissioned this type of treatment in a number of these tumour sites. However challenges remain in delivering the most precise treatment as the tumours are difficult to see or distinguish from normal tissues using xray based imaging that is available on standard treatment machines. A second challenge is that these tumours move and change shape as a result of breathing or digestive motion. These changes can happen within a treatment or from day to day. The MR Linac has superior imaging with the ability to gate and adapt treatments in real time. These tools could be used to reduce normal tissue toxicity whilst increasing target doses safely. We propose an observational study using published guidelines for SABR prescriptions to see if patients can tolerate MR-Linac based treatments. We will use the images acquired to investigate: safe dose escalation; real-time adaptation strategies; imaging that could give us information about geometric tumour and normal tissue changes; how the target and normal tissue respond to treatment using special imaging techniques like diffusion weighted- or oxygen-enhanced MRI.
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