Merging Orthovoltage X-Ray Minibeams spare the proximal tissues while producing a solid beam at the target Journal Article


Authors: Dilmanian, F. A.; Krishnan, S.; McLaughlin, W. E.; Lukaniec, B.; Baker, J. T.; Ailawadi, S.; Hirsch, K. N.; Cattell, R. F.; Roy, R.; Helfer, J.; Kruger, K.; Spuhler, K.; He, Y.; Tailor, R.; Vassantachart, A.; Heaney, D. C.; Zanzonico, P.; Gobbert, M. K.; Graf, J. S.; Nassimi, J. R.; Fatemi, N. N.; Schweitzer, M. E.; Bangiyev, L.; Eley, J. G.
Article Title: Merging Orthovoltage X-Ray Minibeams spare the proximal tissues while producing a solid beam at the target
Abstract: Conventional radiation therapy of brain tumors often produces cognitive deficits, particularly in children. We investigated the potential efficacy of merging Orthovoltage X-ray Minibeams (OXM). It segments the beam into an array of parallel, thin (~0.3 mm), planar beams, called minibeams, which are known from synchrotron x-ray experiments to spare tissues. Furthermore, the slight divergence of the OXM array make the individual minibeams gradually broaden, thus merging with their neighbors at a given tissue depth to produce a solid beam. In this way the proximal tissues, including the cerebral cortex, can be spared. Here we present experimental results with radiochromic films to characterize the method’s dosimetry. Furthermore, we present our Monte Carlo simulation results for physical absorbed dose, and a first-order biologic model to predict tissue tolerance. In particular, a 220-kVp orthovoltage beam provides a 5-fold sharper lateral penumbra than a 6-MV x-ray beam. The method can be implemented in arc-scan, which may include volumetric-modulated arc therapy (VMAT). Finally, OXM’s low beam energy makes it ideal for tumor-dose enhancement with contrast agents such as iodine or gold nanoparticles, and its low cost, portability, and small room-shielding requirements make it ideal for use in the low-and-middle-income countries. © 2019, The Author(s).
Journal Title: Scientific Reports
Volume: 9
ISSN: 2045-2322
Publisher: Nature Publishing Group  
Date Published: 2019-02-04
Start Page: 1198
Language: English
DOI: 10.1038/s41598-018-37733-x
PUBMED: 30718607
PROVIDER: scopus
PMCID: PMC6362296
DOI/URL:
Notes: Article -- Export Date: 1 March 2019 -- Source: Scopus
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  1. Pat B Zanzonico
    355 Zanzonico
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