[Determination and Evaluation of a Tolerance Limit for In Vivo Dosimetry Based on Dose Variations].

Natsumi Abo, Fumiyasu Matsubayashi, Masahiro Kaneko, Yasushi Ito, Yasuo Yoshioka
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引用次数: 0

Abstract

Purpose: We investigated the relationship between dose variation and gamma analysis pass rate in in vivo dosimetry (IVD) and verified the detectivity of errors by using the tolerance of the pass rate determined on a dose variation basis.

Methods: We used a treatment planning system and water-equivalent phantoms to simulate discrepancies between treatment planning and actual irradiation. These discrepancies were created by either deforming structures outlined in the phantom's computed tomography (CT) images or by modifying the CT values within those structures. We performed gamma analysis to compare the intensity distributions of the planned data (including discrepancies) with the distributions acquired by irradiating real phantoms using an electronic portal imaging device (EPID). We investigated the relationship between the gamma analysis pass rate and dose variation with and without the discrepancies.

Results: For gamma analysis pass rates below 70%, a dose variation of approximately 5% was estimated. The accuracy of using the pass rate to predict a dose variation of 5% was 86%. In validation of the prediction, when the gamma analysis pass rate was below 70%, differences were detected in clinical cases with an 82% accuracy.

Conclusion: A method for determining the tolerance of gamma analysis pass rate based on dose variation in phantoms is useful.

[基于剂量变化的体内剂量学耐受极限的确定和评价]。
目的:研究体内剂量测定(IVD)中剂量变化与γ分析通过率的关系,并利用剂量变化对通过率的容忍度验证误差的可探测性。方法:采用治疗计划系统和水等效模型模拟治疗计划与实际辐照之间的差异。这些差异要么是由幻肢计算机断层扫描(CT)图像中轮廓结构的变形造成的,要么是通过修改这些结构内的CT值造成的。我们进行了伽玛分析,以比较计划数据的强度分布(包括差异)与使用电子传送门成像设备(EPID)照射真实幻影所获得的分布。我们研究了伽玛分析通过率和剂量变化之间的关系,有无差异。结果:伽马分析通过率低于70%,估计剂量变化约为5%。使用通过率预测5%的剂量变化的准确度为86%。在预测的验证中,当伽马分析通过率低于70%时,在临床病例中检测到的差异准确率为82%。结论:建立了一种基于模型剂量变化的γ分析通过率耐受性测定方法。
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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