利用多源特征表征预测肺腺癌中Egfr突变状态

Jianhong Cheng, Jin Liu, M. Jiang, H. Yue, Lin Wu, Jianxin Wang
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引用次数: 3

摘要

表皮生长因子受体(EGFR)基因分型对于使用酪氨酸激酶抑制剂治疗肺腺癌的治疗指南至关重要。然而,准确和无创的方法检测EGFR基因是一个持续的挑战。在这项研究中,我们提出了一个混合框架,即HC-DLR,通过融合多源特征,包括低水平手工放射组学(HCR)特征、高水平基于深度学习的放射组学(DLR)特征和人口统计学特征,来无创预测EGFR突变状态。HCR特征首先从从CT图像中提取的大量手工特征中选择。使用预训练的3D DenseNet从CT图像中提取DLR特征。然后,对多源特征表示进行细化和融合,构建HC-DLR模型,以提高EGFR突变的预测性能。该方法在新收集的670例患者数据集上进行了评估。实验结果表明,HC-DLR模型的预测效果令人鼓舞,AUC为0.76,准确率为72.47%,f1评分为71.35%,在预测肺腺癌EGFR突变方面可能具有潜在的临床价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prediction of Egfr Mutation Status in Lung Adenocarcinoma Using Multi-Source Feature Representations
Epidermal growth factor receptor (EGFR) genotyping is essential to treatment guidelines for the use of tyrosine kinase inhibitors in lung adenocarcinoma. However, accurate and noninvasive methods to detect the EGFR gene are ongoing challenges. In this study, we propose a hybrid framework, namely HC-DLR, to noninvasively predict EGFR mutation status by fusing multi-source features including low-level handcrafted radiomics (HCR) features, high-level deep learning-based radiomics (DLR) features, and demographics features. The HCR features first are selected from massive handcrafted features extracted from CT images. The DLR features are also extracted from CT images using the pre-trained 3D DenseNet. Then, multi-source feature representations are refined and fused to build an HC-DLR model for improving the predictive performance of EGFR mutations. The proposed method is evaluated on a newly collected dataset with 670 patients. Experimental results show that the HC-DLR model achieves an encouraging predictive performance with an AUC of 0.76, an accuracy of 72.47%, and an F1-score of 71.35%, which may have potential clinical value for predicting EGFR mutations in lung adenocarcinoma.
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