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Copyright ©The Author(s) 2020.
Artif Intell Gastroenterol. Aug 28, 2020; 1(2): 37-50
Published online Aug 28, 2020. doi: 10.35712/aig.v1.i2.37
Table 2 Application of radiomics in disease staging in gastroenterology
Classification of diseaseImaging modalityFeatures evaluated and methodsOutcomesRef.
Esophageal disease
ESCCUnenhanced CT and CECTSix parameters based on HU values: Mean; 10th percentiles; 90th percentiles; kurtosis; entropy; skewKurtosis and entropy based on unenhanced CT were an independent predictor of T stages, lymph node metastasis (N- vs N+), and overall stages Skew and kurtosis based on unenhanced CT images showed significant differences among N stages as well as 90th percentile based on contrast-enhanced CT images; entropy and 90th percentile based on CECT images showed significant correlations with N stage and overall stage[18]
ESCCCECTA total of 9790 radiomics features were extracted including the following four categories: First-order histogram statistics, size and shape-based features, texture features, and wavelet featuresThe radiomics signature significantly associated with ESCC staging and yielded a better performance for discrimination of early and advanced stage ESCC compared to tumor volume[19]
Gastric disease
GCMRIEntropy-related parameters based on ADC maps including: (1) First-order entropy; (2–5) second-order entropies, including entropy(H)0, entropy(H)45, entropy(H)90, and entropy(H)135; (6) entropy(H)mean; and (7) entropy(H)rangeAll the entropy-related parameters showed significant differences in gastric cancers at different T, N, and overall stages, as well as at different statuses of vascular invasion Entropy, entropy(H)0, entropy(H)45, and entropy(H)90, showed significant differences between gastric cancers with and without perineural invasion[35]
GCCECTMean; maximum frequency; mode; skewness; kurtosis; entropyMaximum frequency in the arterial phase and mean, maximum frequency, mode in the venous phase correlated positively with T, N, and overall stage of GC; entropy in the venous phase also correlated positively with N and overall stage; skewness in the arterial phase had the highest AUC of 0.822 in identifying early from advanced GCs[34]
Hepatic disease
Hepatic fibrosisCECTMean gray-level intensity; entropy; kurtosis; skewnessMean gray-level intensity, mean, and entropy increased with fibrosis stage; kurtosis and skewness decreased with increasing fibrosis[43]
Pancreatic disease
PNETCECTPositive pixels; SD; kurtosis; skewness; entropyEntropy was predictive of Grades 2 and 3 tumors with an accuracy rate for classifying G1, G2, and G3 tumors of 79.3%[53]
PNETCECTMean value; variance; skewness; kurtosis; entropyKurtosis was significantly different among the three G groups, giving an AUC value of 0.924 for the diagnosis of G3 with a sensitivity and specificity of 82% and 85%, respectively; entropy differed significantly between G1 and G3 and between G2 and G3 tumors, giving an AUC value of 0.732 for the diagnosis of G3 with a sensitivity and specificity of 82% and 64%, respectively[54]
Colorectal disease
CRCCECTThe 16-feature-based radiomics signature was generated using LASSO logistic regression modelThe 16-feature-based radiomics signature was an independent predictor for staging of CRC and could categorize CRC into stage I-II and stage III-IV Compared with the clinical model, the radiomics signature showed significantly better performance either in the training dataset (AUC: 0.792 vs 0.632; P < 0.001) or in the validation dataset (AUC: 0.708 vs 0.592; P = 0.037)[59]