Post-irradiation darkening model for EBT-3 films characterized using a single lot calibration approach.

IF 3.3 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Marco Caprioli, Laurence Delombaerde, Robin De Roover, Wouter Crijns
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引用次数: 0

Abstract

Objective.In this study, we present a model to correct the progressive post-irradiation darkening of EBT3 films. The model allows for a clinical use of EBT3 using application and calibration films scanned with different post-irradiation times.Approach.The model is a post-irradiation time- and dose-dependent power-law function, projecting the scanned transmittance of application films to the transmittance matching the same post-irradiation time of calibration films. The model was characterized for two EBT3 production lots within the dose range 0.1-12.8 Gy. A first characterization was performed utilizing calibration films scanned repeatedly for 54 d post-irradiation (lot 1), while a fast re-characterization of a second lot used three post-irradiation times (lot 2). For a long-term validation of the model, 16 film strips were irradiated at 2 Gy on different time points starting from the day of film calibration up to 43 d afterwards (lot 1). For the multiple-dose validation of the model, 8 strips were irradiated with dose levels ranging 0-12 Gy deposited 25 d after the calibration (lot 2). As a proof of principle, the model was applied to four clinical patient-specific quality assurance film measurements with prescribed dose/fraction ranging 2.66 Gy-8 Gy.Main results. The post-irradiation transmittance decreased for higher doses up to -2.5% at 12.8 Gy, and 54 d post-irradiation. With a lot-specific model correction, the mean dose accuracy of validation strips that ranged from initial -3.4% (triple-channel) and -9.90% (blue-channel) reduced to within 3.0% (all colour channels) for doses above 1 Gy. The median dose difference with the planned dose improved from -3.5% to -1.1%, and the 3%/2 mm local gamma ranged from (48.5-92.5)% to (81.2-99.2)%.Significance.A film darkening model corrects the transmittance of EBT3 films and increases the flexibility of existing dosimetry protocols. The correction ensures dose accuracies within 3%.

使用单批次校准方法表征 EBT-3 薄膜的辐照后暗化模型。
研究目的在这项研究中,我们提出了一个模型来纠正 EBT3 胶片在辐照后逐渐变暗的现象。该模型允许使用不同辐照后时间扫描的应用和校准 EBT3 薄膜进行临床应用。该模型是一个与辐照后时间和剂量相关的幂律函数,它将应用薄膜的扫描透射率投影到校准薄膜与相同辐照后时间相匹配的透射率上。在 0.1-12.8 Gy 的剂量范围内,对两个 EBT3 生产批次的模型进行了表征。第一次特征描述是利用校准胶片在辐照后 54 天内反复扫描(批量 1),而第二次批量的快速再特征描述则使用了辐照后的三个时间(批量 2)。 为了对模型进行长期验证,16 个胶片条从胶片校准日开始到辐照后 43 天(批量 1)的不同时间点上进行了 2 Gy 的辐照。为了对模型进行多剂量验证,在校准(批次 2)25 天后,用 0-12 Gy 的剂量水平辐照了 8 片胶片。作为原理验证,该模型被应用于四次临床患者质量保证胶片测量,规定剂量/分量为 2.66 Gy-8 Gy。 辐照后透射率随着剂量的增加而降低,在 12.8 Gy 和 54 天的辐照后透射率为-2.5%。 通过特定批次模型校正,验证条的平均剂量精确度从最初的-3.4%(三通道)和-9. 与计划剂量的中位剂量差从-3.5%提高到-1.1%,3%/2 毫米局部伽马值从 (48.5 - 92.5)% 提高到 (81.2 - 99.2)% 。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Physics in medicine and biology
Physics in medicine and biology 医学-工程:生物医学
CiteScore
6.50
自引率
14.30%
发文量
409
审稿时长
2 months
期刊介绍: The development and application of theoretical, computational and experimental physics to medicine, physiology and biology. Topics covered are: therapy physics (including ionizing and non-ionizing radiation); biomedical imaging (e.g. x-ray, magnetic resonance, ultrasound, optical and nuclear imaging); image-guided interventions; image reconstruction and analysis (including kinetic modelling); artificial intelligence in biomedical physics and analysis; nanoparticles in imaging and therapy; radiobiology; radiation protection and patient dose monitoring; radiation dosimetry
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