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  1. 原著論文

Possibility of increasing linear energy transfer in multi-ion radiotherapy for bone and soft tissue sarcomas

https://repo.qst.go.jp/records/2001882
https://repo.qst.go.jp/records/2001882
6004d1bf-4a05-42b2-baae-c824cbfd7443
アイテムタイプ 学術雑誌論文 / Journal Article(1)
公開日 2025-09-18
タイトル
タイトル Possibility of increasing linear energy transfer in multi-ion radiotherapy for bone and soft tissue sarcomas
言語 en
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
著者 Takei Hideyuki

× Takei Hideyuki

Takei Hideyuki

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Imai Reiko

× Imai Reiko

Imai Reiko

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Masuda Takamitsu

× Masuda Takamitsu

Masuda Takamitsu

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Katsumi Aoki

× Katsumi Aoki

Katsumi Aoki

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Nakaji Taku

× Nakaji Taku

Nakaji Taku

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Nomura Yusuke

× Nomura Yusuke

Nomura Yusuke

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Asami Inomata

× Asami Inomata

Asami Inomata

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Yui Suzuki

× Yui Suzuki

Yui Suzuki

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Inaniwa Taku

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Inaniwa Taku

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抄録
内容記述タイプ Abstract
内容記述 BackgroundMulti-ion radiotherapy using carbon, oxygen, and neon ions aims to improve local control by increasing dose-averaged linear energy transfer (LETd) in the target. However, there has been limited understanding of how to utilize variables for multi-ion treatment planning such as the selection and arrangement of ion species.PurposeAn in silico study was conducted to explore the feasibility of increasing a minimum LETd, and the optimal selection and arrangement of ion species in multi-ion therapy for increasing LETd in tumors of varying sizes mimicking bone and soft tissue sarcomas (BSTS). Additionally, the robustness of multi-ion therapy against setup and range errors was evaluated.MethodsSpherical targets of 500, 1000, and 1500-mL volumes were placed at the center or 80 mm horizontally displaced from the center of a numerical phantom to simulate BSTS treatments. Treatment plans were made for these targets with two orthogonal fields of carbon-only, oxygen+carbon, and neon+carbon ions with a total dose of 70.4 Gy (RBE). The treatment parameters were optimized to increase the LETd in the targets while ensuring adequate target dose coverage and dose homogeneity. The plans were evaluated based on the dose covering 95% of the target (D95%), skin dose (Dskin), and the minimum LETd excluding the 1 mL volume with the lowest LETd (L1mL). Multi-ion radiotherapy treatment plans were also developed for 12 patients with BSTS who had previously received carbon-ion radiotherapy. D95% and L1m of the target, and the dose to organs at risk (OARs) such as the rectum, intestine, and spinal cord were assessed. The robustness of the plans created in the phantom against setup and range errors was evaluated under 2 mm shifts in six directions combined with 2.5% variation of the stopping power ratio, resulting in 12 scenarios. Differences in the target D95% and L1mL, and Dskin in each scenario from those in the nominal plan were evaluated.ResultsThe target dose coverage was comparable for any ion species combinations regardless of target size and position. The L1mL in the target increased by 7–9 and 15–20 keV/µm with the oxygen+carbon and neon+carbon plans, respectively, compared to the carbon-only plans, while maintaining homogeneity index values below 0.10. Additionally, the skin dose increased by 2.2–7.0 and 9.2–14.6 Gy (RBE) for the oxygen+carbon and neon+carbon plans. The L1mL was greater than or equal to 40 keV/µm in all phantom targets and most clinical cases for the oxygen+carbon and neon+carbon plans, while meeting the target and OAR dose requirements. In the robustness evaluation, the variations in D95% were comparable or smaller in the oxygen+carbon and neon+carbon plans than in the carbon-only plan. The maximum decrease in L1mL in the target was 1.5 keV/µm. The maximum increase in Dskin was 2.4 Gy (RBE) in the target closest to the skin.ConclusionsThe LETd was successfully increased with the oxygen+carbon and neon+carbon ions, while meeting the dose requirements. The multi-ion therapy plans created using the method presented in this study were robust to setup and range errors.
書誌情報 Medical Physics

巻 52, 号 9, p. e18097, 発行日 2025-09
DOI
識別子タイプ DOI
関連識別子 10.1002/mp.18097
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