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タイトル: | Microdosimetric quantities of an accelerator-based neutron source used for boron neutron capture therapy measured using a gas-filled proportional counter |
著者: | Hu, Naonori Tanaka, Hiroki Takata, Takushi Okazaki, Keita Uchida, Ryohei Sakurai, Yoshinori https://orcid.org/0000-0001-9404-4255 (unconfirmed) |
著者名の別形: | 田中, 浩基 高田, 卓志 櫻井, 良憲 |
キーワード: | boron neutron capture therapy accelerator-based neutron source tissue equivalent proportional counter microdosimetry |
発行日: | Mar-2020 |
出版者: | Oxford University Press (OUP) |
誌名: | Journal of radiation research |
巻: | 61 |
号: | 2 |
開始ページ: | 214 |
終了ページ: | 220 |
抄録: | Boron neutron capture therapy (BNCT) is an emerging radiation treatment modality, exhibiting the potential to selectively destroy cancer cells. Currently, BNCT is conducted using a nuclear reactor. However, the future trend is to move toward an accelerator-based system for use in hospital environments. A typical BNCT radiation field has several different types of radiation. The beam quality should be quantified to accurately determine the dose to be delivered to the target. This study utilized a tissue equivalent proportional counter (TEPC) to measure microdosimetric and macrodosimetric quantities of an accelerator-based neutron source. The micro- and macro-dosimetric quantities measured with the TEPC were compared with those obtained via the the particle and heavy ion transport code system (PHITS) Monte Carlo simulation. The absorbed dose from events >20 keV/μm measured free in air for a 1-h irradiation was calculated as 1.31 ± 0.02 Gy. The simulated result was 1.41 ± 0.07 Gy. The measured and calculated values exhibit good agreement. The relative biological effectiveness (RBE) that was evaluated from the measured microdosimetric spectrum was calculated as 3.7 ± 0.02, similar to the simulated value of 3.8 ± 0.1. These results showed the PHITS Monte Carlo simulation can simulate both micro- and macro-dosimetric quantities accurately. The RBE was calculated using a single-response function, and the results were compared with those of several other institutes that used a similar method. However, care must be taken when using such a single-response function for clinical application, as it is only valid for low doses. For clinical dose ranges (i.e., high doses), multievent distribution inside the target needs to be considered. |
著作権等: | © The Author(s) 2020. Published by Oxford University Press on behalf of The Japanese Radiation Research Society and Japanese Society for Radiation Oncology. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
URI: | http://hdl.handle.net/2433/258969 |
DOI(出版社版): | 10.1093/jrr/rrz101 |
PubMed ID: | 32030430 |
出現コレクション: | 学術雑誌掲載論文等 |
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