Summary
Eligible participants will undergo 5 sessions of radiation therapy on non-consecutive days over 2 weeks. The radiation therapy will be planned to deliver a higher dose to the core of the tumour and a lower, palliative dose to the periphery.
Participants will have data collected on treatment related adverse events and tumour response to the radiation therapy, and will be asked to complete questionnaires on outcomes such as pain and quality of life.
It is hoped that findings from this study will help develop PABR as a treatment modality for the palliation of bulky tumours.