Journal
CANCERS
Volume 14, Issue 12, Pages -Publisher
MDPI
DOI: 10.3390/cancers14122888
Keywords
spatially fractionated radiation therapy; proton therapy; proton minibeam radiation therapy; multislit collimator; scatterer; peak-to-valley dose ratio
Categories
Funding
- National Cancer Center [NCC-2010290, NCC-2110370]
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The study aims to implement proton minibeam radiation therapy (pMBRT) in clinical proton therapy facilities using a multislit collimator (MSC) and a scattering device. Through simulation and experiments, it has been shown that the combination of MSC and scatterers can successfully achieve pMBRT and demonstrate consistent patterns in dose distribution.
Simple Summary Proton minibeam radiation therapy (pMBRT) using multislit collimator (MSC) and scatterers has been proposed to spare healthy tissues and organs on the beam path and beyond the Bragg peak. An MSC that was much thicker than the maximum range of the proton beam could provide a sufficiently high peak-to-valley dose ratio at the patient's skin, and the scatterers could actively convert the spatially fractionated proton beam to a uniform and broad beam in tumors by changing their thickness. The combination of the MSC and the scatterers can be a good solution for implementing pMBRT in clinical proton therapy facilities. The feasibility of proton minibeam radiation therapy (pMBRT) using a multislit collimator (MSC) and a scattering device was evaluated for clinical use at a clinical proton therapy facility. We fabricated, through Monte Carlo (MC) simulations, not only an MSC with a high peak-to-valley dose ratio (PVDR) at the entrance of the proton beam, to prevent radiation toxicity, but also a scattering device to modulate the PVDR in depth. The slit width and center-to-center distance of the diverging MSC were 2.5 mm and 5.0 mm at the large end, respectively, and its thickness and available field size were 100 mm and 76 x 77.5 mm(2), respectively. Spatially fractionated dose distributions were measured at various depths using radiochromic EBT3 films and also tested on bacterial cells. MC simulation showed that the thicker the MSC, the higher the PVDR at the phantom surface. Dosimetric evaluations showed that lateral dose profiles varied according to the scatterer's thickness, and the depths satisfying PVDR = 1.1 moved toward the surface as their thickness increased. The response of the bacterial cells to the proton minibeams' depth was also established, in a manner similar to the dosimetric pattern. Conclusively, these results strongly suggest that pMBRT can be implemented in clinical centers by using MSC and scatterers.
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