放射学特征作为肺癌组织学亚型分类的诊断因素

Xiang Yao, Ling Mao, Ke Yi, Yuxiao Han, Wentao Li, Ying Xiao, Jun Ji, Qingqing Wang, Ke Ren
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引用次数: 0

摘要

目的:探讨放射组学在计算机断层扫描(CT)分析中的应用,以提高其在肺部的诊断效果,特别是在鉴别鳞状细胞癌(SCC)、肺腺癌(ADC)和小细胞肺癌(SCLC)中的应用。方法:回顾性分析确诊的189例肺癌的病理资料,其中SCC 60例,ADC 69例,SCLC 60例。神经网络用于确定是选择肺窗还是纵隔窗来提取有效的放射学特征。利用最小绝对收缩和选择算子(LASSO)多元逻辑回归模型提取放射性特征的关键特征。接下来,使用受试者工作特征曲线和曲线下面积(AUC)分析来评估放射学特征在训练(129例)和验证队列(60例)中的表现。结果:从人工勾画的肿瘤区域中提取了约295个特征。从纵隔窗CT扫描中提取的特征比肺窗扫描具有更好的预后能力。纵隔窗扫描的平均准确率为0.933。我们的分析显示,从纵隔窗扫描中提取的放射学特征有可能建立一个区分SCC、肺ADC和SCLC的预测模型。在验证队列中,放射学特征诊断SCC和SCLC的性能被证明是有效的,AUC值分别为0.869和0.859。结论:构建了独特的放射组学特征作为不同组织学亚型肺癌的诊断因素。肺癌患者可能会从这个提议的放射特征中受益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Radiomic Signature as a Diagnostic Factor for Classification of Histologic Subtypes of Lung Cancer
Objectives: To discuss the application of radiomics using Computerized Tomography (CT) analysis, for improving its diagnostic efficacy in lung, specifically in distinguishing Squamous Cell Carcinoma (SCC), lung Adenocarcinoma (ADC), and Small Cell Lung Cancer (SCLC). Methods: The pathology of 189 identified cases of lung cancer was analyzed, retrospectively (60 patients with SCC, 69 patients with lung ADC and 60 patients with SCLC). A neural network was used to determine whether the pulmonary or mediastinal window was selected to extract effective radiomic features. The key features of radiomic signature were retrieved by a Least Absolute Shrinkage and Selection Operator (LASSO) multiple logistic regression model. Next, receiver operating characteristic curve and Area Under the Curve (AUC) analysis were used to evaluate the performance of the radiomic signature in both, training(129 patients) and validation cohorts (60 patients). Results: About 295 features were extracted from a manually outlined tumor region. Features extracted from mediastinal window CT scans had a better prognostic ability than pulmonary window scans. The average accuracy for mediastinal window scans was 0.933. Our analysis revealed that the radiomic features extracted from mediastinal window scans had the potential to build a prediction model for distinguishing between SCC, lung ADC, and SCLC. The performance of the radiomic signature to diagnose SCC and SCLC in validation cohorts proved effective, with AUC values of 0.869 and 0.859, respectively. Conclusions: A unique radiomic signature was constructed as a diagnostic factor for different histologic subtypes of lung cancer. Patients with lung cancer may benefit from this proposed radiomic signature.
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