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  1. 原著論文

Reformulation of a clinical-dose system for carbon-ion radiotherapy treatment planning at the National Institute of Radiological Sciences, Japan

https://repo.qst.go.jp/records/47089
https://repo.qst.go.jp/records/47089
2f31748b-3776-4ad1-ab74-17b7aa062482
Item type 学術雑誌論文 / Journal Article(1)
公開日 2015-04-07
タイトル
タイトル Reformulation of a clinical-dose system for carbon-ion radiotherapy treatment planning at the National Institute of Radiological Sciences, Japan
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Inaniwa, Taku

× Inaniwa, Taku

WEKO 470340

Inaniwa, Taku

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Kanematsu, Nobuyuki

× Kanematsu, Nobuyuki

WEKO 470341

Kanematsu, Nobuyuki

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Matsufuji, Naruhiro

× Matsufuji, Naruhiro

WEKO 470342

Matsufuji, Naruhiro

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Kanai, Tatsuaki

× Kanai, Tatsuaki

WEKO 470343

Kanai, Tatsuaki

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Shirai, Toshiyuki

× Shirai, Toshiyuki

WEKO 470344

Shirai, Toshiyuki

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Noda, Koji

× Noda, Koji

WEKO 470345

Noda, Koji

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Tsuji, Hiroshi

× Tsuji, Hiroshi

WEKO 470346

Tsuji, Hiroshi

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Kamada, Tadashi

× Kamada, Tadashi

WEKO 470347

Kamada, Tadashi

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Tsujii, Hirohiko

× Tsujii, Hirohiko

WEKO 470348

Tsujii, Hirohiko

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稲庭 拓

× 稲庭 拓

WEKO 470349

en 稲庭 拓

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兼松 伸幸

× 兼松 伸幸

WEKO 470350

en 兼松 伸幸

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松藤 成弘

× 松藤 成弘

WEKO 470351

en 松藤 成弘

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金井 達明

× 金井 達明

WEKO 470352

en 金井 達明

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白井 敏之

× 白井 敏之

WEKO 470353

en 白井 敏之

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野田 耕司

× 野田 耕司

WEKO 470354

en 野田 耕司

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辻 比呂志

× 辻 比呂志

WEKO 470355

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鎌田 正

× 鎌田 正

WEKO 470356

en 鎌田 正

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辻井 博彦

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WEKO 470357

en 辻井 博彦

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抄録
内容記述タイプ Abstract
内容記述 At the National Institute of Radiological Sciences (NIRS), more than 8,000 patients have been treated for various tumors with carbon-ion (C-ion) radiotherapy in the past 20 years based on a radiobiologically defined clinical-dose system. Through clinical experience, including extensive dose escalation studies, optimum dose-fractionation protocols have been established for respective tumors, which may be considered as the standards in C-ion radiotherapy. Although the therapeutic appropriateness of the clinical-dose system has been widely demonstrated by clinical results, the system incorporates several oversimplifications such as dose-independent relative biological effectiveness (RBE), empirical nuclear fragmentation model, and use of dose-averaged linear energy transfer to represent the spectrum of particles. We took the opportunity to update the clinical-dose system at the time we started clinical treatment with pencil beam scanning, a new beam delivery method, in 2011. The requirements for the updated system were to correct the oversimplifications made in the original system, while harmonizing with the original system to maintain the established dose-fractionation protocols. In the updated system, the radiation quality of the therapeutic C-ion beam was derived with Monte Carlo simulations, and its biological effectiveness was predicted with a theoretical model. We selected the most used C-ion beam with αr = 0.764Gy-1 and β = 0.0615Gy-2 as reference radiation for RBE. The C-equivalent biological dose distribution is designed to allow the prescribed survival of tumor cells of the human salivary gland (HSG) in entire spread-out Bragg peak (SOBP) region, with consideration to the dose dependence of the RBE. This C-equivalent biological dose distribution is scaled to a clinical dose distribution to harmonize with our clinical experiences with C-ion radiotherapy. Treatment plans were made with the original and the updated clinical-dose systems, and both physical and clinical dose distributions were compared with regard to the prescribed dose level, beam energy, and SOBP width. Both systems provided uniform clinical dose distributions within the targets consistent with the prescriptions. The mean physical doses delivered to targets by the updated system agreed with the doses by the original system within+-1.5% for all tested conditions. The updated system reflects the physical and biological characteristics of the therapeutic C-ion beam more accurately than the original system, while at the same time allowing the continued use of the dose-fractionation protocols established with the original system at NIRS.
書誌情報 Physics in Medicine and Biology

巻 60, 号 8, p. 3271-3286, 発行日 2015-03
出版者
出版者 IOP Publishing
ISSN
収録物識別子タイプ ISSN
収録物識別子 0031-9155
DOI
識別子タイプ DOI
関連識別子 10.1088/0031-9155/60/8/3271
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