論文

査読有り 国際誌
2020年2月6日

Microdosimetric quantities of an accelerator-based neutron source used for boron neutron capture therapy measured using a gas-filled proportional counter.

Journal of radiation research
  • Naonori Hu
  • ,
  • Hiroki Tanaka
  • ,
  • Takushi Takata
  • ,
  • Keita Okazaki
  • ,
  • Ryohei Uchida
  • ,
  • Yoshinori Sakurai

61
2
開始ページ
214
終了ページ
220
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1093/jrr/rrz101

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.

リンク情報
DOI
https://doi.org/10.1093/jrr/rrz101
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/32030430
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246059
ID情報
  • DOI : 10.1093/jrr/rrz101
  • PubMed ID : 32030430
  • PubMed Central 記事ID : PMC7246059

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