Shiraishi Satomi, Tan Jun, Olsen Lindsey A, Moore Kevin L
Department of Radiation Medicine and Applied Sciences, University of California, San Diego, La Jolla, California 92093.
Department of Radiation Oncology, UT Southwestern Medical Center, Dallas, Texas 75490.
Med Phys. 2015 Feb;42(2):908. doi: 10.1118/1.4906183.
The objective of this work was to develop a comprehensive knowledge-based methodology for predicting achievable dose-volume histograms (DVHs) and highly precise DVH-based quality metrics (QMs) in stereotactic radiosurgery/radiotherapy (SRS/SRT) plans. Accurate QM estimation can identify suboptimal treatment plans and provide target optimization objectives to standardize and improve treatment planning.
Correlating observed dose as it relates to the geometric relationship of organs-at-risk (OARs) to planning target volumes (PTVs) yields mathematical models to predict achievable DVHs. In SRS, DVH-based QMs such as brain V10Gy (volume receiving 10 Gy or more), gradient measure (GM), and conformity index (CI) are used to evaluate plan quality. This study encompasses 223 linear accelerator-based SRS/SRT treatment plans (SRS plans) using volumetric-modulated arc therapy (VMAT), representing 95% of the institution's VMAT radiosurgery load from the past four and a half years. Unfiltered models that use all available plans for the model training were built for each category with a stratification scheme based on target and OAR characteristics determined emergently through initial modeling process. Model predictive accuracy is measured by the mean and standard deviation of the difference between clinical and predicted QMs, δQM = QMclin - QMpred, and a coefficient of determination, R(2). For categories with a large number of plans, refined models are constructed by automatic elimination of suspected suboptimal plans from the training set. Using the refined model as a presumed achievable standard, potentially suboptimal plans are identified. Predictions of QM improvement are validated via standardized replanning of 20 suspected suboptimal plans based on dosimetric predictions. The significance of the QM improvement is evaluated using the Wilcoxon signed rank test.
The most accurate predictions are obtained when plans are stratified based on proximity to OARs and their PTV volume sizes. Volumes are categorized into small (VPTV < 2 cm(3)), medium (2 cm(3) < VPTV < 25 cm(3)), and large (25 cm(3) < VPTV). The unfiltered models demonstrate the ability to predict GMs to ∼1 mm and fractional brain V10Gy to ∼25% for plans with large VPTV and critical OAR involvements. Increased accuracy and precision of QM predictions are obtained when high quality plans are selected for the model training. For the small and medium VPTV plans without critical OAR involvement, predictive ability was evaluated using the refined model. For training plans, the model predicted GM to an accuracy of 0.2 ± 0.3 mm and fractional brain V10Gy to 0.04 ± 0.12, suggesting highly accurate predictive ability. For excluded plans, the average δGM was 1.1 mm and fractional brain V10Gy was 0.20. These δQM are significantly greater than those of the model training plans (p < 0.001). For CI, predictions are close to clinical values and no significant difference was observed between the training and excluded plans (p = 0.19). Twenty outliers with δGM > 1.35 mm were identified as potentially suboptimal, and replanning these cases using predicted target objectives demonstrates significant improvements on QMs: on average, 1.1 mm reduction in GM (p < 0.001) and 23% reduction in brain V10Gy (p < 0.001). After replanning, the difference of δGM distribution between the 20 replans and the refined model training plans was marginal.
The results demonstrate the ability to predict SRS QMs precisely and to identify suboptimal plans. Furthermore, the knowledge-based DVH predictions were directly used as target optimization objectives and allowed a standardized planning process that bettered the clinically approved plans. Full clinical application of this methodology can improve consistency of SRS plan quality in a wide range of PTV volume and proximity to OARs and facilitate automated treatment planning for this critical treatment site.
本研究旨在开发一种基于综合知识的方法,用于预测立体定向放射外科/放疗(SRS/SRT)计划中可实现的剂量体积直方图(DVH)以及基于DVH的高精度质量指标(QM)。准确的QM估计可以识别次优治疗计划,并提供目标优化目标,以规范和改进治疗计划。
将观察到的剂量与危及器官(OAR)与计划靶体积(PTV)的几何关系相关联,从而得出预测可实现DVH的数学模型。在SRS中,基于DVH的QM,如脑V10Gy(接受10Gy或更高剂量的体积)、梯度测量(GM)和适形指数(CI),用于评估计划质量。本研究涵盖了223个基于直线加速器的SRS/SRT治疗计划(SRS计划),这些计划采用容积调强弧形治疗(VMAT),占该机构过去四年半VMAT放射外科治疗量的95%。针对每个类别,使用基于目标和OAR特征的分层方案,构建了未经过滤的模型,这些模型使用所有可用计划进行模型训练,目标和OAR特征是通过初始建模过程紧急确定的。模型预测准确性通过临床和预测QM之间差异的均值和标准差δQM = QMclin - QMpred以及决定系数R²来衡量。对于计划数量较多的类别,通过从训练集中自动排除疑似次优计划来构建优化模型。以优化模型作为假定的可实现标准,识别潜在的次优计划。通过基于剂量学预测对20个疑似次优计划进行标准化重新规划,验证QM改善的预测。使用Wilcoxon符号秩检验评估QM改善的显著性。
当根据与OAR的接近程度及其PTV体积大小对计划进行分层时,可获得最准确的预测。体积分为小(VPTV < 2 cm³)、中(2 cm³ < VPTV < 25 cm³)和大(25 cm³ < VPTV)三类。未经过滤的模型显示,对于VPTV大且关键OAR受累的计划,能够将GM预测到约1mm,将脑部分V10Gy预测到约25%。当选择高质量计划进行模型训练时,QM预测的准确性和精度会提高。对于无关键OAR受累的小和中VPTV计划,使用优化模型评估预测能力。对于训练计划,模型预测GM的精度为0.2 ± 0.3mm,脑部分V10Gy为0.04 ± 0.12,表明具有高度准确的预测能力。对于排除的计划,平均δGM为1.1mm,脑部分V10Gy为0.20。这些δQM显著大于模型训练计划的δQM(p < 0.001)。对于CI,预测接近临床值,训练计划和排除计划之间未观察到显著差异(p = 0.19)。确定了20个δGM > 1.35mm的异常值为潜在次优,使用预测的目标对这些病例进行重新规划显示QM有显著改善:平均GM降低1.1mm(p < 0.001),脑V10Gy降低23%(p < 0.001)。重新规划后,20个重新规划计划与优化模型训练计划之间的δGM分布差异很小。
结果表明能够精确预测SRS QM并识别次优计划。此外,基于知识的DVH预测直接用作目标优化目标,并允许进行标准化的规划过程,从而改善临床批准的计划。该方法的全面临床应用可以提高广泛PTV体积和与OAR接近程度范围内SRS计划质量的一致性,并促进该关键治疗部位的自动化治疗计划。