| Literature DB >> 33199785 |
Mengfan Song1,2, Jing Lin1,2, Fuzhen Song3, Dan Wu4,5, Zhaoxia Qian3.
Abstract
Carcinoma in situ (CIS) of the uterine cervix is a precursor to cervical carcinoma. However, hysterectomy can be avoided in patients who can be treated by cone biopsy. Previous studies have shown that imaging-based approaches allow for the noninvasive visualization of cervical cancer, and radiomics has high accuracy in classifying cancer and predicting treatment outcome for different cancer types. To develop a magnetic resonance (MR)-based radiomics model for identifying residual disease in patients with CIS after cervical conization. Patients who had CIS after conization and finally underwent hysterectomy were collected to comprise a database to establish an imaging model for predicting the residual status after conization. Then, patients who opted for uterine preservation were classified as high-risk or low-risk patients according to the model. The disease-free survival was compared between the different risk groups using the Kaplan-Meier curve. The model built with the Boruta features outperformed the random forest model. Further validation with patients with uterine preservation showed that the patients classified as high risk were more likely to have tumor recurrence/residual disease in the follow-up period. In conclusion, radiomics can be used to identify residual disease in patients with CIS after cervical conization and could have the potential to predict recurrence in patients who opt for uterine preservation.Entities:
Mesh:
Year: 2020 PMID: 33199785 PMCID: PMC7670468 DOI: 10.1038/s41598-020-76853-1
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379
A summary of the extracted and selected radiomics features.
| Extracted radiomics features | All-relevant features (Boruta) | |||
|---|---|---|---|---|
| T2WI | ADC | T2WI | ADC | |
| First order features | “InterquartileRang”,“Skewness”,“Uniformity”,“Median”,“Energy”,“RobustMeanAbsoluteDeviation”,“MeanAbsoluteDeviation”,“Maximum”,“RootMeanSquared”,“90Percentile”,“Minimum”,“Range”,“Variance”,“10Percentile”,“Kurtosis”,“Mean” | Range, Uniformity | MeanAbsoluteDeviation, Kurtosis | |
| Shape features | “Maximum3DDiameter”,“Maximum2DDiameterSlice”,“Sphericity”,“MinorAxis”,“VolumeRatio”,“Volume”,“MajorAxis”,“SurfaceArea”,“Flatness”,“LeastAxis”,“Maximum2DDiameterColumn”,“Maximum2DDiameterRow” | |||
| GLCM/GLDM features | “GrayLevelVariance”,“HighGrayLevelEmphasis”,“DependenceEntropy”,“DependenceNonUniformity”,“GrayLevelNonUniformity”,“SmallDependenceEmphasis”,“SmallDependence”,“HighGrayLevelEmphasis”,“LargeDependenceEmphasis”,“LargeDependenceLowGrayLevelEmphasis”,“DependenceVariance”,“DependenceHighGrayLevelEmphasis”,“LowGrayLevelEmphasis”,“JointAverage”,“SumAverage”,“ClusterShade”,“Idmn”,“JointEnergy”,“Contrast”,“DifferenceEntropy”,“InverseVariance”,“DifferenceVariance”,“Idn”,“Idm”,“Correlation”,“Autocorrelation”,“SumSquares”,“ClusterProminence”,“DifferenceAverage”,“ClusterTendency” | ClusterShade, DependenceVariance | DifferenceEntropy | |
| GLRLM features | “ShortRunLowGrayLevelEmphasis”,“GrayLevelVariance”,“LowGrayLevelRunEmphasis”,“GrayLevelNonUniformityNormalized”,“RunVariance”,“GrayLevelNonUniformity”,“LongRunEmphasis”,“ShortRunHighGrayLevelEmphasis”,“RunLengthNonUniformity”,“ShortRunEmphasis”,“LongRunHighGrayLevelEmphasis”,“RunPercentage”,“LongRunLowGrayLevelEmphasis”,“HighGrayLevelRunEmphasis”,“RunLengthNonUniformityNormalized” | RunLengthNonUniformityNormalized | RunVariance | |
| GLSZM features | “GrayLevelVariance”,“ZoneVariance”,“GrayLevelNonUniformityNormalized”,“SizeZoneNonUniformityNormalized”,“SizeZoneNonUniformity”,“GrayLevelNonUniformity”,“SmallAreaHighGrayLevelEmphasis”,“ZonePercentage”,“LargeAreaLowGrayLevelEmphasis”,“LargeAreaHighGrayLevelEmphasis”,“HighGrayLevelZoneEmphasis”,“SmallAreaEmphasis”,“LowGrayLevelZoneEmphasis”,“ZoneEntropy”,“SmallAreaLowGrayLevelEmphasis” | SmallAreaHighGrayLevelEmphasis, LargeAreaLowGrayLevelEmphasis | SizeZoneNonUniformityNormalized | |
| NGTDM features | “Coarseness, Complexity”,“Strength”,“Contrast”,“Busyness” | Contrast | ||
Figure 1Heatmap of the normalized feature value distribution of the 13 all-relevant features to differentiate between residual and nonresidual disease.
Figure 2ROC curves of the random forest and all-relevant models for identifying residual disease in the training (a) and test (b) cohort.
Internal validation of the performances of RandomForest model, Boruta model for differentiating residual and nonresidual disease.
| Training group | Test group | |||||
|---|---|---|---|---|---|---|
| RF | Boruta | PM | RF | Boruta | PM | |
| AUC | 0.899 | 0.959 | 0.630 | 0.701 | 0.889 | 0.679 |
| Accuracy | 0.891 | 0.963 | 0.636 | 0.721 | 0.873 | 0.691 |
| Sensitive | 0.722 | 0.944 | 0.611 | 0.706 | 0.824 | 0.647 |
| Specificity | 0.973 | 0.973 | 0.649 | 0.749 | 0.895 | 0.711 |
| PPV | 0.929 | 0.944 | 0.572 | 0.667 | 0.778 | 0.591 |
| NPV | 0.878 | 0.973 | 0.734 | 0.805 | 0.919 | 0.758 |
RF RandomForest, PM positive margin.
Figure 3The Kaplan–Meier curve of the radiomics model for identifying high- and low-risk patients in the validation group.
Figure 4The flowchart of segmentation procedure.