Liu X, Li J, Schild S E, Schild M H, Wong W, Vora S, Herman M G, Fatyga M
School of Computing, Informatics and Decision Systems Engineering, Arizona State University, USA.
Department of Radiation Oncology, Mayo Clinic Arizona, USA.
OMICS J Radiol. 2018;7(5). doi: 10.4172/2167-7964.1000302. Epub 2018 Dec 3.
Intensity Modulated Radiation Therapy (IMRT) allows for significant dose reductions to organs at risk in prostate cancer patients. However, the accurate delivery of IMRT plans can be compromised by patient positioning errors. The purpose of this study was to determine if the modeling of grade ≥ 2 acute rectal toxicity could be used to monitor the quality of IMRT protocols.
79 patients treated with Image and Fiducial Markers Guided IMRT (FMIGRT) and 302 patients treated with trans-abdominal ultrasound guided IMRT (USGRT) was selected for this study. Treatment plans were available for the FMIGRT group, and hand recorded dosimetric indices were available for both groups. We modeled toxicity in the FMIGRT group using the Lyman Kutcher Burman (LKB) and Univariate Logistic Regression (ULR) models, and we modeled toxicity in USGRT group using the ULR model. We performed Receiver Operating Characteristics (ROC) analysis on all of the models and compared the Area under the ROC curve (AUC) for the FMIGRT and the USGRT groups.
The observed Incidence of grade ≥ 2 rectal toxicity was 20% in FMIGRT patients and 54% in USGRT patients. LKB model parameters in the FMIGRT group were TD=56.8 Gy, slope m=0.093, and exponent n=0.131. The most predictive indices in the ULR model for the FMIGRT group were D and V. AUC for both models in the FMIGRT group was similar (AUC=0.67). The FMIGRT URL model predicted less than a 37% incidence of grade ≥ 2 acute rectal toxicity in the USGRT group. A fit of the ULR model to USGRT data did not yield a predictive model (AUC=0.5).
Modeling of acute rectal toxicity provided a quantitative measure of the correlation between planning dosimetry and this clinical endpoint. Our study suggests that an unusually weak correlation may indicate a persistent patient positioning error.
调强放射治疗(IMRT)能够显著降低前列腺癌患者危及器官的受量。然而,患者摆位误差可能会影响IMRT计划的精确实施。本研究旨在确定≥2级急性直肠毒性的模型是否可用于监测IMRT方案的质量。
本研究选取了79例接受影像和基准标记引导的IMRT(FMIGRT)治疗的患者以及302例接受经腹超声引导的IMRT(USGRT)治疗的患者。FMIGRT组有治疗计划,两组均有手工记录的剂量学指标。我们使用莱曼-库彻-伯曼(LKB)模型和单变量逻辑回归(ULR)模型对FMIGRT组的毒性进行建模,使用ULR模型对USGRT组的毒性进行建模。我们对所有模型进行了受试者操作特征(ROC)分析,并比较了FMIGRT组和USGRT组的ROC曲线下面积(AUC)。
FMIGRT组中观察到的≥2级直肠毒性发生率为20%,USGRT组为54%。FMIGRT组的LKB模型参数为TD = 56.8 Gy,斜率m = 0.093,指数n = 0.131。FMIGRT组ULR模型中最具预测性的指标是D和V。FMIGRT组两个模型的AUC相似(AUC = 0.67)。FMIGRT组的ULR模型预测USGRT组≥2级急性直肠毒性的发生率低于37%。ULR模型对USGRT数据的拟合未产生预测模型(AUC = 0.5)。
急性直肠毒性的建模提供了计划剂量学与该临床终点之间相关性的定量测量。我们的研究表明,异常弱的相关性可能表明存在持续的患者摆位误差。