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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 3 Application of radiomics in evaluation of therapeutic efficacy and prognosis in gastroenterology
Classification of diseaseImaging modalityFeatures evaluated and methodsOutcomesRef.
Esophageal disease
EC18F-FDG PETA total of 38 features (such as entropy, size, and magnitude of local and global heterogeneous and homogeneous tumor regions) extracted from 5 different texturesTumor textural analysis provided non-responder, partial-responder, and complete-responder patient identification with a higher sensitivity (76%-92%) than any SUV measurement[22]
ESCCMRI138 radiomic features were extracted from each image sequence based on three principal methods: Histogram-based (IH, GH), texture-based (GLCM, GLRLM, and NIDM), and transform-based (GWTF)Radiomic analysis showed that CR vs SD, PR vs SD, and responders (CR and PR) vs non- responders could be differentiated by 26, 17, and 33 features, respectively; the prediction models (ANN and SVM) based on features extracted from SPAIR T2W sequence (SVM: 0.929; ANN: 0.883) showed higher accuracy than those derived from T2W (SVM: 0.893; ANN: 0.861)[24]
Gastric disease
GCCECTHistogram features: Kurtosis, skewness; GLCM: ASM, contrast, entropy, variance, correlationContrast, variance, and correlation showed fair accuracy for the prediction of good survival with all AUCs being over 0.7, and all were statistically significant[38]
Hepatic disease
HCCCECT21 textural parameters per filter were extracted from the region of interests delineated around tumor outline by application of a Gabor filter and wavelet transform with 3 band-width responses (filter 0, 1.0, and 1.5)Texture analysis was observed to have potential in assessment of prognosis and selection of appropriate patients with intermediate-advanced HCC treated by TACE and sorafenib[46]
HCCCECTFirst order statistics; geometry; texture analysis; GLCMTextures derived from pretreatment dynamic CT imaging were analyzed, higher arterial enhancement ratio and GLCM moments, smaller tumor size, and lower tumor homogeneity were significant predictors of CR after TACE[47]
Pancreatic disease
Pancreas head cancerCECTLaplacian of the Gaussian band-pass filter was applied to detect intensity changes within the images smoothened by Gaussian distribution based on the filter sigma value of 1.0 (fine texture, filter width 4 pixels), 1.5 to 2.0 (medium texture, filter width 6-10 pixels), and 2.5 (coarse texture, filter width 12 pixels)Texture parameters of average, contrast, correlation, and standard deviation with no filter, and fine to medium filter values, as well as the presence of nodal metastasis were significantly different between recurred and non-recurred patients; lower standard deviation and contrast and higher correlation with lower average value representing homogenous texture were significantly associated with poorer DFS, along with the presence of lymph node metastasis[55]
PDACCECTMean gray-level; intensity; entropy; MPP; kurtosis; SD; skewnessTumor size, tumor SD, and skewness were significantly and independently associated with PFS, while tumor size and tumor SD were significantly and independently associated with OS[56]
Colorectal disease
LARCMRI18 features extracted using the Haralick's GLCM and 12 parameters calculated for the histogram-based analysisRadiomics based on pre-treatment and early follow-up MRI could provide quantitative information to differentiate pCR from non-pCR, and GR from non-GR.[60]
Rectal cancerMRIKurtosis; entropy; skewness; MPPThe change in kurtosis between midtreatment and pretreatment images was significantly lower in the PR + NR subgroup compared with the pCR subgroup; pretreatment AUROC to discriminate between pCR and PR + NR, was significantly higher for kurtosis (0.907, P < 0.001)[61]