临床前电子闪光放射生物学用线性加速器的无创可逆软件配置。

ArXiv Pub Date : 2025-09-25
Stavros Melemenidis, Dixin Chen, Cody Jensen, Joseph B Schulz, Murat Surucu, Amy S Yu, Edward E Graves, Mengying Shi, Peter G Maxim, Andrew Currell, Billy W Loo Jr, Lawrie Skinner, M Ramish Ashraf
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引用次数: 0

摘要

配置用于超高剂量率(UHDR)电子实验的临床线性加速器(linacs)通常需要侵入性的硬件操作和/或不可逆的制造商修改,限制了更广泛的实施。我们提出了一种独立开发的临床TrueBeam直线加速器的UHDR电子配置,它允许在临床前UHDR和传统(CONV)模式之间进行可逆切换,仅使用非侵入性软件设置。UHDR模式通过服务模式软件实现,设置典型的光子束的射频和光束电流,光子靶和监测室缩回,插入临床未使用的低能散射箔。附件托盘上安装了用于光束监测的外部交流电流互感器(ACCT),解剖专用准直器和样品支架,固体水中的外部离子室用于出口剂量监测。测量了UHDR和CONV光束的百分比深度剂量(PDD)。通过调节枪电压来改变每脉冲剂量(DPP),并在不同的源表面距离(SSD)下用放射性致色膜进行量化。光束分布评估剂量均匀性和可用场大小。在膜、ACCT和离子室之间建立剂量校准,并测试日常的重复性。PDD证实了UHDR (12.8MeV)和CONV (11.9MeV)光束的能量相似,且通过鼠标厚度具有匹配的轮廓。最大DPP超过0.5Gy,体内准直设置达到~1.5Gy,组织培养扩展SSD达到~0.7Gy。电场平坦和对称保持,支持器官特异性照射和高达5厘米的培养场。校正结果显示各检测器之间线性关系强,输出变化为
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non-invasive Reversible Software-based Configuration of a Clinically Used Linear Accelerator for Preclinical Electron FLASH Radiobiology.

Configuring clinical linear accelerators (linacs) for ultra-high dose rate (UHDR) electron experiments typically requires invasive hardware manipulation and/or irreversible manufacturer modifications, limiting broader implementation. We present an independently developed UHDR electron configuration of a clinical TrueBeam linac that allows reversible switching between preclinical UHDR and conventional (CONV) modes using only non-invasive software settings. UHDR mode was achieved via service mode software with RF and beam current settings typical of a photon beam, the photon target and monitor chamber retracted, and a clinically unused low-energy scattering foil inserted. An external AC current transformer (ACCT) for beam monitoring, anatomy-specific collimator, and sample holder were mounted on the accessory tray, with external ion chamber in solid water for exit dose monitoring. Percent depth dose (PDD) was measured for UHDR and CONV beams. Dose-per-pulse (DPP) was varied by adjusting gun voltage and quantified with radiochromic film at different source-to-surface distances (SSD). Beam profiles assessed dose uniformity and usable field size. Dose calibration was established between film, ACCT, and ion chamber, and day-to-day reproducibility was tested. PDD confirmed similar energies for UHDR (12.8MeV) and CONV (11.9MeV) beams with matching profiles through mouse thickness. Maximum DPP exceeded 0.5Gy, reaching ~1.5Gy for collimated in vivo setups and ~0.7Gy at extended SSD for tissue culture. Field flatness and symmetry were maintained, supporting organ-specific irradiations and up to 5cm fields for culture. Calibration showed strong linearity across detectors, and output variation was <4%. We demonstrated accurate, reproducible UHDR delivery on a widely available clinical linac with no invasive hardware manipulation, enabling preclinical FLASH research on a clinical treatment machine.

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