Proton minibeam radiation therapy (pMBRT) dose profile is characterized by highly heterogeneous dose in the plane perpendicular to the beam direction and rapidly changing depth dose profiles. Typically, dose measurements are benchmarked against in-house Monte Carlo simulation tools. It is essential to have a treatment planning system (TPS) that can accurately predict pMBRT doses in tissue and be available via commercial platform for preclinical and clinical use. Methods: The pMBRT beam model was implemented in RayStation for the IBA Proteus®ONE single-room compact proton machine. The RayStation pMBRT beam model is an add-on to the clinically used beam model. The adjustable parameters include air gap, slit thickness, slit pitch, number of slits, slits direction and slit thickness. The pMBRT TPS is validated experimentally against measurements. Six different collimators with various slit widths and center-to-center slit distance are used. The slit width varies from 0.4 mm to 1.4 mm, and the center to center (c-t-c) distance varies from 2.8 mm to 4.0 mm. The slits are non-divergent with a total of 5 slits. Results: When comparing the average depth dose measurements against the RayStation dose MC calculation, the agreement is better than a 95% gamma passing rate using 3mm/3% criteria except the 0.4 mm slit width. However, after we adjusted the slit width by 40 - 60 μm to account for machining uncertainty, the agreement again exceeds a 95% gamma passing rate using 3mm/3% criteria. When comparing the PDDs of the peaks and valleys between RayStation and film measurements, the agreement is above 90% using 2mm/5% criteria. When comparing later profiles at various depths, the agreement is above 90% for all curves using 0.2mm/5%. Conclusions: The pMBRT beam modeling has been successfully established for our Proteus®ONE-based pMBRT system using the RayStation TPS, with demonstrated accuracy through experimental validation.
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http://dx.doi.org/10.1088/1361-6560/adae4f | DOI Listing |
Phys Med Biol
January 2025
Department of Radiation Oncology, The University of Kansas Medical Center, Department of Radiation Oncology, University of Kansas Medical Center, USA, Kansas City, Kansas, 66160-8500, UNITED STATES.
Proton minibeam radiation therapy (pMBRT) dose profile is characterized by highly heterogeneous dose in the plane perpendicular to the beam direction and rapidly changing depth dose profiles. Typically, dose measurements are benchmarked against in-house Monte Carlo simulation tools. It is essential to have a treatment planning system (TPS) that can accurately predict pMBRT doses in tissue and be available via commercial platform for preclinical and clinical use.
View Article and Find Full Text PDFCancers (Basel)
November 2024
Radiotherapy and Radiation Dosimetry, National Physical Laboratory, Teddington TW11 0LW, UK.
Med Phys
November 2024
Department of Radiation Oncology, University of Kansas Medical Center, Kansas City, Kansas, USA.
Background: The clinical translation of proton minibeam radiation therapy (pMBRT) presents significant challenges, particularly in developing an optimal treatment planning technique. A uniform target dose is crucial for maximizing anti-tumor efficacy and facilitating the clinical acceptance of pMBRT. However, achieving a high peak-to-valley dose ratio (PVDR) in organs-at-risk (OAR) is essential for sparing normal tissue.
View Article and Find Full Text PDFRadiother Oncol
December 2024
Institut Curie, Université PSL, CNRS UMR3347, Inserm U1021, Signalisation Radiobiologie et Cancer, 91400 Orsay, France; Université Paris-Saclay, CNRS UMR3347, Inserm U1021, Signalisation Radiobiologie et Cancer, 91400 Orsay, France. Electronic address:
Phys Med Biol
October 2024
Orsay Proton Therapy Center, Institut Curie, Orsay, France.
Proton radiotherapy's efficacy relies on an accurate relative stopping power (RSP) map of the patient to optimise the treatment plan and minimize uncertainties. Currently, a conversion of a Hounsfield Units map obtained by a common x-ray computed tomography (CT) is used to compute the RSP. This conversion is one of the main limiting factors for proton radiotherapy.
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