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Collimated and non-collimated proton minibeam irradiation using SIRMIO: a simulation study.
Fardous Reaz1, Ze Huang2, Marco Pinto2
1Department of Clinical Medicine, Aarhus University, Aarhus, Denmark; Danish Centre for Particle Therapy, Aarhus University Hospital, Aarhus, Denmark. fardous@clin.au.dk.
Acta Oncologica (Stockholm, Sweden)
|November 3, 2025
Summary
The SIRMIO platform effectively delivers spatially fractionated proton doses for preclinical proton MBRT research. Simulations show it achieves high dose contrast, essential for advancing this radiation oncology technique.
Area of Science:
- Radiation Oncology
- Medical Physics
- Preclinical Research
Background:
- Clinical integration of proton MBRT requires understanding parameter-effect relationships.
- Small animal models are crucial for these investigations.
- A specialized platform is needed for precise spatial dose control in preclinical studies.
Purpose of the Study:
- To evaluate the SIRMIO beamline's capability for proton MBRT experiments.
- To assess dose delivery configurations with and without a multislit collimator.
- To investigate the impact of center-to-center spacing on dose fractionation.
Main Methods:
- In silico study using Geant4-based Monte Carlo simulations.
- Evaluated two beamline configurations: no collimator and with a brass multislit collimator (MSC).
- Simulated center-to-center spacings of 3, 4, and 5 mm, with a 1 mm slit width for the MSC configuration.
Main Results:
- SIRMIO generates effective spatially fractionated dose profiles with varying center-to-center (CTC) spacing.
- Sufficient dose contrast for pMBRT achieved with CTC ≥ 4 mm (PVDR 3.44-6.57) without collimator.
- MSC enhanced dose contrast significantly (PVDR 11.3-28.7) for CTC 3-5 mm.
- Interlacing beams demonstrated potential for uniform target dose with preserved normal tissue contrast.
Conclusions:
- The SIRMIO platform is a viable tool for preclinical proton MBRT research.
- The platform can deliver precisely controlled spatially fractionated doses.
- Simulations confirm its potential for advancing pMBRT investigations.

