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Dose calibration of EPIDs for segmented IMRT dosimetry

机译:用于分段IMRT剂量测定的EPID剂量校准

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The purpose of this study was to investigate the dose response of amorphous silicon (a-Si) electronic portal imaging devices (EPIDs) under different acquisition settings for both open jaw defined fields and segmented intensity-modulated radiation therapy (IMRT) fields. Four different EPIDs were used. Two Siemens and one Elekta plus a standalone Perkin Elmer research EPID. Each was operated with different acquisition systems and settings. Dose response linearity was measured for open static jaw defined fields and ‘simple’ segmented IMRT fields for a range of equipment and system settings. Six ‘simple’ segmented IMRT fields were used. The segments of each IMRT field were fixed at 10 × 10 cm 2 field size with equal MU per segment, each field having a total of 20 MU. Simultaneous measurements with an ionization chamber array (ICA) and EPID were performed to separate beam and detector response characteristics. Three different pixel calibration methods were demonstrated and compared for an example ‘clinical IMRT field’. The dose response with the Elekta EPID for ‘simple’ segmented IMRT fields versus static fields agreed to within 2.5% for monitor unit ( MU ) ≥ 2 . The dose response for the Siemens systems was difficult to interpret due to the poor reproducibility for segmented delivery, at MU ≤ 5 , which was not observed with the standalone research EPID nor ICA on the same machine. The dose response measured under different acquisition settings and different linac/EPID combinations matched closely ( ≤ 1 % ), except for the Siemens EPID. Clinical IMRT EPID dosimetry implemented with the different pixel-to-dose calibration methods indicated that calibration at 20 MU provides equivalent results to implementing a ghosting correction model. The nonlinear dose response was consistent across both clinical EPIDs and the standalone research EPID, with the exception of the poor reproducibility seen with Siemens EPID images of IMRT fields. The nonlinear dose response was relatively insensitive to acquisition settings and appears to be primarily due to gain ghosting effects. No additional ghosting correction factor is necessary when the pixel-to-dose calibration factor at small MU calibration method is used.PACS numbers: 87.53.Bn, 87.55.Qr, 87.56.Fc, 87.57.uq
机译:这项研究的目的是研究开放式颌骨定义场和分段强度调制放射治疗(IMRT)场在不同采集设置下非晶硅(a-Si)电子门成像设备(EPID)的剂量响应。使用了四个不同的EPID。两台西门子和一台Elekta加上独立的Perkin Elmer研究型EPID。每个系统都使用不同的采集系统和设置进行操作。针对开放的静态颌定义字段和“简单”分段IMRT字段,针对一系列设备和系统设置,测量了剂量响应线性。使用了六个“简单”细分的IMRT字段。每个IMRT场的段固定为10×10 cm 2场大小,每个段的MU相等,每个场总计20 MU。用电离室阵列(ICA)和EPID进行了同时测量,以分离出电子束和检测器的响应特性。演示了三种不同的像素校准方法,并以“临床IMRT领域”为例进行了比较。对于监测单元(MU)≥2,使用Elekta EPID的“简单”分段IMRT场与静态场的剂量响应在2.5%之内。由于在MU≤5时分段递送的可重复性差,西门子系统的剂量响应难以解释,而在同一台机器上使用独立研究EPID或ICA则未观察到。在不同的采集设置和不同的直线加速器/ EPID组合下测得的剂量响应紧密匹配(≤1%),除了西门子EPID。使用不同的像素到剂量的校准方法实施的临床IMRT EPID剂量测定表明,在20 MU处进行校准可提供与实现重影校正模型等效的结果。跨临床EPID和独立研究EPID的非线性剂量响应均一致,除了IMRT领域的Siemens EPID图像所见的重现性差。非线性剂量响应对采集设置相对不敏感,并且似乎主要归因于增益重影效应。当使用小MU校准方法的像素到剂量校准因子时,不需要其他的重影校正因子.PACS编号:87.53.Bn,87.55.Qr,87.56.Fc,87.57.uq

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