In this study, a radiomics approach was extended to optical fluorescence molecular imaging data for tissue classification, termed 'optomics'. Fluorescence molecular imaging is emerging for precise surgical guidance during head and neck squamous cell carcinoma (HNSCC) resection. However, the tumor-to-normal tissue contrast is confounded by intrinsic physiological limitations of heterogeneous expression of the target molecule, epidermal growth factor receptor (EGFR). Optomics seek to improve tumor identification by probing textural pattern differences in EGFR expression conveyed by fluorescence. A total of 1,472 standardized optomic features were extracted from fluorescence image samples. A supervised machine learning pipeline involving a support vector machine classifier was trained with 25 top-ranked features selected by minimum redundancy maximum relevance criterion. Model predictive performance was compared to fluorescence intensity thresholding method by classifying testing set image patches of resected tissue with histologically confirmed malignancy status. The optomics approach provided consistent improvement in prediction accuracy on all test set samples, irrespective of dose, compared to fluorescence intensity thresholding method (mean accuracies of 89% vs. 81%; P = 0.0072). The improved performance demonstrates that extending the radiomics approach to fluorescence molecular imaging data offers a promising image analysis technique for cancer detection in fluorescence-guided surgery.
翻译:在本研究中,对组织分类的光荧光分子成像数据采用了放射法,称为“optomics ” 。在头部和颈部粘合细胞癌分解期间,正在出现精确的外科指导的荧光分子成像。然而,肿瘤与正常组织对比是由目标分子、上皮生长因子受体的多元表达方式(EGFR)的内在生理局限性所混杂的。 optomics试图通过对通过荧光显示的EGBFR表达方式的纹理模式差异来改进肿瘤识别。从荧光图像样本中提取了总共1,472个标准化的选制成特征。一个由支持矢量机分类(HNSCC)组成的受监督的机器学习管道接受了25个顶级特征的培训,这些特征由最小冗余最大相关性标准所选择。模型的预测性能与荧光强度临界值的临界值方法相比较,通过对测试所设定的受精度组织成像部分和经心理学确认的恶性状态来改进肿瘤识别。 选情学方法为所有测试样品的预测准确度提供了一致的精确度,而不论剂量的剂量的剂量为多少度;精度的精度分析方法的精度,比值为81度分析的精度;度的精度分析的精度为焦度的精度分析。