Mutual information-based feature selection for radiomics

被引:3
|
作者
Oubel, Estanislao [1 ]
Beaumont, Hubert [1 ]
Iannessi, Antoine [2 ]
机构
[1] Median Technol, Valbonne, France
[2] Ctr Antoine Lacassagne, 36 Voie Romaine, F-06054 Nice, France
关键词
feature selection; radiomics; big data; mutual information; clinical trials; oncology; biomarkers; response to treatment; prediction; LESIONS; RECIST; NUMBER;
D O I
10.1117/12.2216746
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
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.
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页数:9
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