Bhandari Ashok, Johnson Kurtis, Oh Kyuhak, Yu Fang, Huynh Linda M, Lei Yu, Wisnoskie Sarah, Zhou Sumin, Baine Michael James, Lin Chi, Zhang Chi, Wang Shuo
Department of Radiation Oncology, University of Nebraska Medical Center, Omaha, NE, United States.
Department of Biostatistics, University of Nebraska Medical Center, Omaha, NE, United States.
Front Oncol. 2024 Dec 12;14:1438861. doi: 10.3389/fonc.2024.1438861. eCollection 2024.
The purpose of this study was to investigate the dosiomics features of the interplay between CT density and dose distribution in lung SBRT plans, and to develop a model to predict treatment failure following lung SBRT treatment.
A retrospective study was conducted involving 179 lung cancer patients treated with SBRT at the University of Nebraska Medical Center (UNMC) between October 2007 and June 2022. Features from the CT image, Biological Effective Dose (BED) and five interaction matrices between CT and BED were extracted using radiomics mathematics. Our in-house feature selection pipeline was utilized to evaluate and rank features based on their importance and redundancy, with only the selected non-redundant features being used for predictive modeling. We randomly selected 151 cases and 28 cases as training and test datasets. Four different models were trained utilizing the Balanced Random Forest framework on the same training dataset to differentiate between failure and non-failure cases. These four models utilized the same number of selected features extracted from CT-only, BED-only, a combination of CT and BED, and a composite of CT and BED including their interaction matrices, respectively.
The cohort included 125 non-failure cases and 54 failure cases, with a median follow-up time of 34.4 months. We selected the top 17 important and non-redundant features (with the Pearsons's coefficient < 0.5) in each model. When evaluated on the same independent test set, the four models-CT features-only, BED features-only, a combination of CT and BED features, and a composite model including features from CT and BED that includes their interaction matrices-achieved AUC values of 0.56, 0.75, 0.73, and 0.82, respectively, with corresponding accuracies of 0.61, 0.79, 0.71, and 0.79. The composite model demonstrated the highest AUC and accuracy, indicating that incorporating interactions between CT and BED reveals more predictive capabilities in distinguishing between failure and non-failure cases.
The dosiomics model integrating the interaction between CT and Dose can effectively predict treatment failure following lung SBRT treatment and may serve as a useful tool to proactively evaluate and select lung SBRT treatment plans to reduce treatment failure in the future.
本研究旨在探讨肺部立体定向体部放疗(SBRT)计划中CT密度与剂量分布相互作用的剂量组学特征,并建立一个模型来预测肺部SBRT治疗后的治疗失败情况。
进行了一项回顾性研究,纳入了2007年10月至2022年6月期间在内布拉斯加大学医学中心(UNMC)接受SBRT治疗的179例肺癌患者。使用放射组学数学方法从CT图像、生物等效剂量(BED)以及CT与BED之间的五个相互作用矩阵中提取特征。我们利用内部特征选择流程,根据特征的重要性和冗余性对其进行评估和排序,仅将选定的非冗余特征用于预测建模。我们随机选择151例和28例分别作为训练和测试数据集。在相同的训练数据集上,利用平衡随机森林框架训练了四种不同的模型,以区分失败和非失败病例。这四种模型分别利用了从仅CT、仅BED、CT和BED的组合以及包括其相互作用矩阵的CT和BED的复合体中提取的相同数量的选定特征。
该队列包括125例非失败病例和54例失败病例,中位随访时间为34.4个月。我们在每个模型中选择了前17个重要且非冗余的特征(皮尔逊系数<0.5)。在相同的独立测试集上进行评估时,四个模型——仅CT特征、仅BED特征、CT和BED特征的组合以及包括来自CT和BED的特征及其相互作用矩阵的复合模型——的AUC值分别为0.56、0.75、0.73和0.82,相应的准确率分别为0.61、0.79、0.71和0.79。复合模型显示出最高 的AUC值和准确率,表明纳入CT和BED之间的相互作用在区分失败和非失败病例方面具有更强的预测能力。
整合CT与剂量之间相互作用的剂量组学模型能够有效预测肺部SBRT治疗后的治疗失败情况,并且可能成为未来主动评估和选择肺部SBRT治疗计划以减少治疗失败的有用工具。