1st Department of Medicine, Poznan University of Medical Sciences, Poznan, Poland.
Department of Medical Physics, International Oncology Center Affidea, Poznan, Poland.
PLoS One. 2019 Aug 13;14(8):e0221086. doi: 10.1371/journal.pone.0221086. eCollection 2019.
To evaluate methods for the pre-treatment verification of volumetric modulated arc therapy (VMAT) based on the percentage gamma passing rate (%GP) and its correlation and sensitivity with percentage dosimetric errors (%DE).
A total of 25 patients with prostate cancer and 15 with endometrial cancer were analysed. The %GP values of 2D and 3D verifications with different acceptance criteria (1%/1 mm, 2%/2 mm, and 3%/3 mm) were obtained using OmniPro and Compass. The %DE was calculated using a planned dose volume histogram (DVH) created in Monaco's treatment planning system (TPS), which relates radiation dose to tissue and the patient's predicted dose volume histogram in Compass. Statistical correlation between %GP and %DE was verified using Pearson's correlation coefficient. Sensitivity was calculated based on the receiver operating characteristics (ROC) curve. Plans were calculated using Collapsed Cone Convolution and the Monte Carlo algorithm.
The t-test results of the planned and estimated DVH showed that the mean values were comparable (P > 0.05). For the 3%/3 mm criterion, the average %GP was acceptable for the prostate and endometrial cancer groups, with average rates of 99.68 ± 0.49% and 99.03 ± 0.59% for 2D and 99.86 ± 0.39% and 99.53 ± 0.44% for 3D, respectively. The number of correlations was poor for all analysed data. The mean Pearson's R-values for prostate and endometrial cancer were < 0.45 and < 0.43, respectively. The area under the ROC curve for the prostate and endometrial cancer groups, was lower than 0.667.
Analysis of the %GP versus %DE values revealed only weak correlations between 2D and 3D verifications. DVH results obtained using the Compass system will be helpful in confirming that the analysed plans respect dosimetric constraints.
评估基于百分比剂量误差(%DE)和百分比剂量误差(%DE)的相关性和敏感性的容积调强弧形治疗(VMAT)预处理验证方法。
分析了 25 例前列腺癌和 15 例子宫内膜癌患者。使用 OmniPro 和 Compass 获得了不同接受标准(1%/1mm、2%/2mm 和 3%/3mm)的 2D 和 3D 验证的%GP 值。使用 Monaco 治疗计划系统(TPS)中的计划剂量体积直方图(DVH)计算%DE,该系统将辐射剂量与组织和 Compass 中的患者预测剂量体积直方图相关联。使用 Pearson 相关系数验证%GP 与%DE 之间的统计相关性。基于接收者操作特征(ROC)曲线计算灵敏度。使用 Collapsed Cone Convolution 和 Monte Carlo 算法计算计划。
计划和估计的 DVH 的 t 检验结果表明平均值相当(P > 0.05)。对于 3%/3mm 标准,前列腺和子宫内膜癌组的平均%GP 是可以接受的,2D 的平均率分别为 99.68 ± 0.49%和 99.03 ± 0.59%,3D 的平均率分别为 99.86 ± 0.39%和 99.53 ± 0.44%。所有分析数据的相关性都很差。前列腺和子宫内膜癌的平均 Pearson R 值分别小于 0.45 和 0.43。前列腺和子宫内膜癌组的 ROC 曲线下面积均低于 0.667。
%GP 与%DE 值的分析表明,2D 和 3D 验证之间仅存在微弱的相关性。使用 Compass 系统获得的 DVH 结果将有助于确认分析计划符合剂量学约束。