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Optimizing Monoscopic kV Fluoro Acquisition for Prostate Intrafraction Motion Evaluation

机译:优化单视场kV含氟量采集以评估前列腺内运动

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摘要

Monoscopic kV imaging during radiotherapy has been recently implemented for prostate intrafraction motion evaluation. However, the accuracy of 3D localization techniques from monoscopic imaging of prostate and the effect of acquisition parameters on the 3D accuracy have not been studied in detail, with imaging dose remaining a concern. In this paper we investigate methods to optimize the kV acquisition parameters and imaging protocol to achieve improved 3D localization and 2D image registration accuracy for minimal imaging dose. Prostate motion during radiotherapy was simulated using existing cine-MRI measurements, and was used to investigate the accuracy of various 3D localization techniques and the effect of kV acquisition protocol. We also investigated the relationship between mAs and the accuracy of the 2D image registration for localization of fiducial markers, and we measured imaging dose for a 30-cm diameter phantom to evaluate the necessary dose to achieve acceptable image registration accuracy. Simulations showed that the error in assuming the shortest path to localize the prostate in 3D using monoscopic imaging during a typical IMRT fraction will be less than ~1.5 mm for 95% of localizations, but will also depend on prostate motion distribution, treatment duration, and image acquisition and treatment protocol. Most uncertainty cannot be reduced from higher imaging frequency or acquiring during gantry rotation between beams. Measured maximum surface dose to the cylindrical phantom from monoscopic kV intrafraction acquisitions varied between 0.4–5.5 mGy, depending on acquisition protocol, and was lower than the required dose for CBCT (21.1 mGy). Imaging dose can be lowered by ~15–40% when mAs is optimized with acquisition angle. Images acquired during MV beam delivery require increased mAs to obtain the same level of registration accuracy, with mAs/registration increasing roughly linearly with field size and dose rate.
机译:放射治疗期间的单眼kV成像最近已用于前列腺内运动评估。但是,尚未详细研究来自前列腺的单眼成像的3D定位技术的精度以及采集参数对3D精度的影响,而成像剂量仍然值得关注。在本文中,我们研究了优化kV采集参数和成像协议的方法,从而以最小的成像剂量实现了改进的3D定位和2D图像配准精度。使用现有的cine-MRI测量值对放疗期间的前列腺运动进行了模拟,并用于研究各种3D定位技术的准确性以及kV采集协议的影响。我们还研究了mAs与2D图像配准的基准标记定位精度之间的关系,并测量了直径为30 cm的体模的成像剂量,以评估获得可接受的图像配准精度所需的剂量。仿真显示,在典型的IMRT分数期间,使用单镜成像在3D中假设定位前列腺的最短路径的误差在95%的定位范围内将小于〜1.5 mm,但还取决于前列腺运动分布,治疗时间和图像采集和处理协议。大多数不确定性无法通过较高的成像频率或在梁之间的机架旋转过程中获得来降低。单视场kV级分数内采集测量到的圆柱体模最大表面剂量在0.4-5.5 mG​​y之间变化,具体取决于采集方案,并且低于CBCT所需的剂量(21.1 mGy)。当采用采集角度优化mAs时,成像剂量可降低约15–40%。在MV光束传输过程中获取的图像需要增加mAs才能获得相同水平的配准精度,而mAs /配准随场大小和剂量率大致呈线性增加。

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