在纳入研究的300例乳腺结节患者中,术后病理学检查结果为良性199例,恶性101例。瘤内超声影像组学模型在训练组曲线下面积(area under curve,AUC)为0.927(95% CI 0.889~0.965),验证组的AUC为0.808(95% CI 0.710~0.905),验证组的准确度、灵敏度、特异度、F1值、精确度分别为0.753、0.731、0.763、0.644、0.576。瘤周超声影像组学模型在训练组AUC为0.930(95% CI 0.891~0.969),验证组的AUC为0.857(95% CI 0.763~0.949),验证组的准确度、灵敏度、特异度、F1值、精确度分别为0.812、0.846、0.797、0.733、0.647。瘤内联合瘤周超声影像组学特征在训练组SVM模型的AUC为0.941(95% CI 0.843~0.967),验证组AUC为0.865(95% CI 0.781~0.949),验证组的准确度、灵敏度、特异度、F1值、精确度分别为0.824、0.692、0.881、0.706、0.720。瘤内瘤周超声影像组学特征结合临床变量的模型在训练集AUC为0.952(95% CI 0.924~0.979),验证组AUC为0.873(95% CI 0.788~0.958),验证组的准确度、灵敏度、特异度、F1值、精确度分别为0.859、0.692、0.932、0.750、0.818。瘤内瘤周联合临床变量模型的诊断效能均优于临床变量组、瘤内影像组学模型,
To investigate the value of ultrasound-based peri-tumoral radiomics in discriminating benign and malignant breast nodules.
Methods:
A total of 300 cases of breast masses patients who were screened by regular ultrasound examination in The Sixth People’s Hospital
Shanghai Jiao Tong University School of Medicine were retrospectively collected. For、 the lesion on the regular ultrasound image
the largest dimension was selected to outline the region of interest. Subsequently
this area was automatically expanded by 2 mm in all directions
conformally and outwardly
to extract intra- and peritumor radiomics features. The included cases were randomly divided into a training group (210 cases) and a validation group (90 cases) in a ratio of 7∶3. Apply the least absolute shrinkage and selection operator (LASSO) to perform feature selection and obtain the optimal featurecombination. The optimal features of the included models were retained by dimensionality reduction of the imaging omics features. The support vector machine (SVM) model was used to classify benign and malignant breast nodules
and evaluate the diagnostic efficacy of ultrasonic breast nodules by the receiver operating characteristics (ROC) curve.
Results:
Among 300 breast nodules
101 were malignant nodules and 199 were benign nodules. The ultrasound-based intra-tumoral radiomics model had an area under curve (AUC) value of 0.927 (95% CI 0.889-0.965) in the training group and 0.808 (95% CI 0.710-0.905) in the validation group. The accuracy
sensitivity
specificity
F1 value
and precision were 0.753
0.731
0
.763
0.644
and 0.576 in the validation group
respectively in the ultrasound-based intra-tumoral radiomics model. The ultrasound-based peri-tumoral radiomics model had an AUC value of 0.930 (95% CI 0.891-0.969) in the training group and 0.857 (95% CI 0.763-0.949) in the validation group
and the accuracy
sensitivity
specificity
F1 value
and precision of this model were 0.812、0.846、0.797、0.733、0.647 for the validation group
respectively in the ultrasound-based peri-tumoral radiomics model. The intratumorally combined with peritumoral ultrasound imaging histological features had an AUC value of 0.941 (95% CI 0.843-0.967) in the training group and 0.865 (95% CI 0.781-0.949) in the validation group
the accuracy
sensitivity
specificity
F1 value
and precision of the model were 0.824
0.692
0.881
0.706
0.720 in the validation group
respectively. The model with intra-perineural radiomics features combined with clinical variables had an AUC value of 0.952 (95% CI 0.924-0.979) in the training set and an AUC value of 0.873 (95% CI: 0.788 to 0.958) in the validation group
and the accuracy
sensitivity
specificity
F1 value
and precision of the validation group were 0.859
0.692
0.932
0.750
and 0.818
respectively. The diagnostic efficacy of the intra-peri-tumoral combined with clinical variables model was better than that of the clinical variables group and intratumoral imaging histology
with statistically significant differences (
P
<0.05); it was higher than that of the peri-tumoral and intratumoral combined with peri-tumoral models
but the differences were not statistically significant (
P
>0.05).
Conclusion:
Both intra-tumoral and peri-tumoral ultrasound radiomics have high value in the diagnosis of benign and malignant breast nodules. The application of intra-tumoral and peri-tumoral radiomics can reduce the missed rate of breast cancer and unnecessary biopsies.