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An investigation of the depth dose in the build-up region, and surface dose for a 6-MV therapeutic photon beam: Monte Carlo simulation and measurements

机译:研究6-MV治疗性光子束在累积区域的深度剂量和表面剂量:蒙特卡洛模拟和测量

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The MC simulations were based on the EGSnrc code system, developed by the National Research Council of Canada (NRC) [25, 26]. The 6-MV photon beam generated from a Varian Clinac 23EX medical linear accelerator was simulated using the BEAMnrc user code. The dose distribution in a phantom was obtained by the use of the DOSXYZnrc user code. The Varian Clinac 23EX linear accelerator, equipped with a Millennium 120-leaf MLC and on-board imaging system, located at the Department of Radiation Oncology, Siriraj Hospital, Thailand, was used in this study. All measurements were performed on the 6-MV photon beam along the central axis with square open field sizes of 5 × 5, 10 × 10, 15 × 15 and 20 × 20 cm2at a constant source-to-surface distance of 100 cm. The complete percentage depth doses were measured in a Blue water phantom (Wellhofer Scanditronix, Germany) at a depth ranging from 0 to 30 cm with a scanning resolution of 2 mm. The detectors used with this water phantom were a compact cylindrical ionization chamber of type CC13 (Wellhofer Scanditronix, Germany) and a silicon p-type photon semiconductor dosimeter of type PFD (Wellhofer Scanditronix, Germany). The CC13 dosimeter has an active diameter of 6 mm, a cavity volume of 0.13 cm3, and a wall thickness of 0.07 g/cm2. The PFD dosimeter has an active diameter of 2 mm and an effective thickness of 0.06 mm from the detector's front surface. These two dosimeters are routinely used to acquire the common beam data, such as the percentage depth dose, the beam profiles and the output factor. The depth doses along the central axis of the beam were obtained for different square field sizes of our 6-MV photon beam simulation using the DOSXYZnrc code. They were normalized as a percentage of the maximum dose. Here, the percentage dose near or at the phantom surface was estimated by the third-order polynomial extrapolation of the simulated data. The observed percentage doses at the surface and at a depth of 0.0007 and 0.005 mm were compared with the published results of Devic et al. [13] and Parsai et al. [19], since they had performed reliable measurements of the surface dose and the dose in the build-up region at the same beam energy from similar medical linear accerelators (the Varian Clinac 1800 and the Varian 2300 (C/D), respectively). Accordingly, a substantial discrepancy in the dose in the build-up region from our MC simulation-based calculations and their previously reported empirical measurements was not anticipated. Table 1summarizes the dose comparison using the MC simulation results obtained here and the previously measured values [13, 19] for the square fields with lengths of 5, 10 and 15 cm. Consistent results were generally observed in which all of the differences were less than 2%. Therefore, we conclude that our calculated surface doses using the MC simulation were justified. The percentage depth doses along the beam central axis for our 6-MV photon beams were acquired experimentally with four detectors for the four square field sizes of 5 × 5, 10 × 10, 15 × 15 and 20 × 20 cm2. The readings from each detector were assigned to the effective point of measurement for each individual detector. For the CC13 chamber, the effective point was determined automatically by the computerized scanning system. The effective point of measurement for the PFD dosimeter and Markus chamber was assumed to be at the front surface and at the bottom of the entrance window electrode, respectively. For the TLD chip, the effective point was assigned to the middle of its thickness and scaled by its density of 0.0496 g/cm2. From the extrapolation of the measured dose in the build-up region, the percentage doses at zero depth (surface doses) for the 6-MV photon beam with different field sizes are shown in Fig. 3. The measured surface dose clearly increases with increasing field size, regardless of the detector used in the measurement, and this is also observed with the MC simulation. This is mainly due to the increasing number of scattered electrons in the air and collimator. The measurements obtained from the TLD chip and Markus chamber gave surface dose values close to that of the MC simulation, while a very large discrepancy was found when using the PFD dosimeter and, especially, the CC13 chamber. Before scaling of the effective depth of measurement, the over-response of the TLD chip and Markus chamber for the surface dose were about 10%, which is consistent with the reports of Devic et al. [13] and Gerbi and Khan [16]. After taking into account the effective point of measurement, the over-response from the TLD chip was reduced to approximately 4%, while that for the Markus chamber remained almost unchanged due to its larger effective volume.
机译:MC仿真基于加拿大国家研究委员会(NRC)开发的EGSnrc代码系统[25,26]。使用BEAMnrc用户代码模拟了Varian Clinac 23EX医用线性加速器产生的6-MV光子束。幻像中的剂量分布是通过使用DOSXYZnrc用户代码获得的。这项研究使用了位于泰国Siriraj医院放射肿瘤科的Varian Clinac 23EX线性加速器,该加速器配备了千年120叶MLC和车载成像系统。所有测量均沿中心轴在6-MV光子束上进行,并在恒定光源下以5×5、10×10、15×15和20×20 cm 2 的正方形开场大小进行。到表面的距离为100厘米。在蓝色水体模(Wellhofer Scanditronix,德国)中,在0至30 cm的深度范围内以2 mm的扫描分辨率测量完整的深度剂量百分比。与该水模一起使用的检测器是CC13型紧凑型圆柱电离室(德国,Wellhofer Scanditronix)和PFD型硅p型光子半导体剂量计(德国,Wellhofer Scanditronix)。 CC13剂量计的有效直径为6 mm,腔体积为0.13 cm 3 ,壁厚为0.07 g / cm 2 。 PFD剂量计的有效直径为2毫米,有效厚度为距检测器前表面0.06毫米。这两个剂量计通常用于获取公共光束数据,例如深度剂量百分比,光束轮廓和输出因子。使用DOSXYZnrc代码,针对我们的6-MV光子束模拟的不同平方场大小,获得了沿束中心轴的深度剂量。将它们标准化为最大剂量的百分比。在此,通过模拟数据的三阶多项式外推法估算了幻影表面附近或幻影表面的剂量百分比。将表面和深度为0.0007和0.005 mm处观察到的百分比剂量与Devic等人的已发表结果进行了比较。 [13]和Parsai等。 [19],因为他们已经从类似的医用线性加速器(分别为Varian Clinac 1800和Varian 2300(C / D))以相同的束能量对表面剂量和积聚区域中的剂量进行了可靠的测量。 。因此,我们的基于MC模拟的计算及其先前报道的经验测量结果在积聚区域的剂量上不会出现实质性差异。表1使用此处获得的MC模拟结果和长度为5、10和15 cm的正方形场的先前测量值[13、19]总结了剂量比较。通常观察到一致的结果,其中所有差异均小于2%。因此,我们得出结论,使用MC模拟计算出的表面剂量是合理的。用四个探测器通过实验获得了6-MV光子束沿束中心轴的深度剂量百分比,这四个探测器的4个正方形场大小分别为5×5、10×10、15×15和20×20 cm 2 < / sup>。每个检测器的读数分配给每个检测器的有效测量点。对于CC13腔室,有效点由计算机扫描系统自动确定。假定PFD剂量计和Markus室的有效测量点分别在入射窗电极的前表面和底部。对于TLD芯片,有效点被分配到其厚度的中间,并按其密度0.0496 g / cm 2 进行缩放。从建立区域的测量剂量推算,图3显示了具有不同视场大小的6-MV光子束在零深度处的剂量百分比(表面剂量)。测量的表面剂量显然随着增加而增加场大小,而与测量中使用的检测器无关,MC模拟也可以观察到。这主要是由于空气和准直仪中散射电子数量的增加。从TLD芯片和Markus腔室获得的测量值给出的表面剂量值接近MC模拟值,而使用PFD剂量计,尤其是CC13腔室时,发现非常大的差异。在缩放有效测量深度之前,TLD芯片和Markus腔室对表面剂量的过度响应约为10%,这与Devic等人的报告一致。 [13]和Gerbi和Khan [16]。考虑到有效的测量点后,来自TLD芯片的过响应减少到了大约4%,而Markus腔的过响应由于其较大的有效体积而几乎保持不变。

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