Department of Breast Surgery, Second Affiliated Hospital of Dalian Medical University, 467, Zhongshan Road, Shahekou District, Dalian, Liaoning 116023, China.
Biomed Res Int. 2022 May 26;2022:1376659. doi: 10.1155/2022/1376659. eCollection 2022.
Image texture information was extracted from enhanced magnetic resonance imaging (MRI) and pathological hematoxylin and eosin- (HE-) stained images of female breast cancer patients. We established models individually, and then, we combine the two kinds of data to establish model. Through this method, we verified whether sufficient information could be obtained from enhanced MRI and pathological slides to assist in the determination of epidermal growth factor receptor (EGFR) mutation status in patients.
We obtained enhanced MRI data from patients with breast cancer before treatment and selected diffusion-weighted imaging (DWI), T1 fast-spin echo (T1 FSE), and T2 fast-spin echo (T2 FSE) as the data sources for extracting texture information. Imaging physicians manually outlined the 3D regions of interest (ROIs) and extracted texture features according to the gray level cooccurrence matrix (GLCM) of the images. For the HE staining images of the patients, we adopted a specific normalization algorithm to simulate the images dyed with only hematoxylin or eosin and extracted textures. We extracted texture features to predict the expression of EGFR. After evaluating the predictive power of each model, the models from the two data sources were combined for remodeling.
For enhanced MRI data, the modeling of texture information of T1 FSE had a good predictive effect for EGFR mutation status. For pathological images, eosin-stained images can achieve a better prediction effect. We selected these two classifiers as the weak classifiers of the final model and obtained good results (training group: AUC, 0.983; 95% CI, 0.95-1.00; accuracy, 0.962; specificity, 0.936; and sensitivity, 0.979; test group: AUC, 0.983; 95% CI, 0.94-1.00; accuracy, 0.943; specificity, 1.00; and sensitivity, 0.905).
The EGFR mutation status of patients with breast cancer can be well predicted based on enhanced MRI data and pathological data. This helps hospitals that do not test the EGFR mutation status of patients with breast cancer. The technology gives clinicians more information about breast cancer, which helps them make accurate diagnoses and select suitable treatments.
从女性乳腺癌患者增强磁共振成像(MRI)和病理苏木精和伊红(HE)染色图像中提取图像纹理信息。我们分别建立模型,然后将两种数据结合起来建立模型。通过这种方法,我们验证了从增强 MRI 和病理切片中是否可以获得足够的信息来帮助确定患者表皮生长因子受体(EGFR)突变状态。
我们从接受治疗前的乳腺癌患者中获得增强 MRI 数据,并选择弥散加权成像(DWI)、T1 快速自旋回波(T1 FSE)和 T2 快速自旋回波(T2 FSE)作为提取纹理信息的数据源。影像医师根据图像的灰度共生矩阵(GLCM)手动勾勒出 3D 感兴趣区(ROI)并提取纹理特征。对于患者的 HE 染色图像,我们采用特定的归一化算法来模拟仅用苏木精或伊红染色的图像,并提取纹理。我们提取纹理特征来预测 EGFR 的表达。在评估每个模型的预测能力后,对来自两种数据源的模型进行组合重建。
对于增强 MRI 数据,T1 FSE 纹理信息的建模对 EGFR 突变状态具有良好的预测效果。对于病理图像,伊红染色图像可以达到更好的预测效果。我们选择这两个分类器作为最终模型的弱分类器,取得了较好的结果(训练组:AUC 为 0.983;95%CI,0.95-1.00;准确率为 0.962;特异性为 0.936;敏感性为 0.979;测试组:AUC 为 0.983;95%CI,0.94-1.00;准确率为 0.943;特异性为 1.00;敏感性为 0.905)。
基于增强 MRI 数据和病理数据可以很好地预测乳腺癌患者的 EGFR 突变状态。这有助于那些不检测乳腺癌患者 EGFR 突变状态的医院。该技术为临床医生提供了更多有关乳腺癌的信息,有助于他们做出准确的诊断并选择合适的治疗方法。