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Mutual information-based feature selection for radiomics

机译:基于互联网的相互信息的特征选择

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Background The extraction and analysis of image features (radiomics) is a promising field in the precision medicine era, with applications to prognosis, prediction, and response to treatment quantification. In this work, we present a mutual information - based method for quantifying reproducibility of features, a necessary step for qualification before their inclusion in big data systems. Materials and Methods Ten patients with Non-Small Cell Lung Cancer (NSCLC) lesions were followed over time (7 time points in average) with Computed Tomography (CT). Five observers segmented lesions by using a semi-automatic method and 27 features describing shape and intensity distribution were extracted. Inter-observer reproducibility was assessed by computing the multi-information (MI) of feature changes over time, and the variability of global extrema. Results The highest MI values were obtained for volume-based features (VBF). The lesion mass (M), surface to volume ratio (SVR) and volume (V) presented statistically significant higher values of MI than the rest of features. Within the same VBF group, SVR showed also the lowest variability of extrema. The correlation coefficient (CC) of feature values was unable to make a difference between features. Conclusions MI allowed to discriminate three features (M, SVR, and V) from the rest in a statistically significant manner. This result is consistent with the order obtained when sorting features by increasing values of extrema variability. MI is a promising alternative for selecting features to be considered as surrogate biomarkers in a precision medicine context.
机译:背景技术图像特征的提取和分析(adrioMICS)是精密医学时代的有希望的领域,具有预后,预测和治疗量化的响应。在这项工作中,我们介绍了一种基于相同的信息 - 用于量化特征的重复性,在其包含在大数据系统中的符合要求之前的必要步骤。材料和方法10例非小细胞肺癌(NSCLC)病变伴随时间(平均值7个时间点),具有计算机断层扫描(CT)。通过使用半自动方法和描述形状和强度分布的27个特征来分割病变和描述形状和强度分布的27个观察者。通过计算功能变化的多信息(MI)以及全球极值的可变性来评估观察者间再现性。结果获得基于体积的特征(VBF)的最高MI值。病变质量(m),表面到体积比(SVR)和体积(V)呈现比其余特征的统计学显着的MI值。在同一VBF组中,SVR也显示了极值的最低变异性。特征值的相关系数(CC)无法在功能之间产生差异。结论MI允许以统计显着的方式在其余部分中区分三个特征(M,SVR和V)。该结果与通过增加极值变异性的值来排序特征时获得的顺序一致。 MI是在精确药物背景下选择被视为替代生物标志物的特征的有前途的替代方案。

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