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Evaluation of a deep learning architecture for MR imaging prediction of ATRX in glioma patients

机译:评估胶质瘤患者ATRX先生成像预测的深层学习架构

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Predicting mutation/loss of alpha-thalassemia/mental retardation syndrome X-linked (ATRX) gene utilizing MR imaging is of high importance since it is a predictor of response and prognosis in brain tumors. In this study, we compare a deep neural network approach based on a residual deep neural network (ResNet) architecture and one based on a classical machine learning approach and evaluate their ability in predicting ATRX mutation status without the need for a distinct tumor segmentation step. We found that the ResNet50 (50 layers) architecture, pre trained on ImageNet data was the best performing model, achieving an accuracy of 0.91 for the test set (classification of a slice as no tumor, ATRX mutated, or mutated) in terms of fl score in a test set of 35 cases. The SVM classifier achieved 0.63 for differentiating the Flair signal abnormality regions from the test patients based on their mutation status. We report a method that alleviates the need for extensive preprocessing and acts as a proof of concept that deep neural network architectures can be used to predict molecular biomarkers from routine medical images.
机译:利用MR成像的预测突变/丧失α-地产血症/发育迟滞综合征X-链接(ATRX)基因具有很高的重要性,因为它是脑肿瘤的响应和预后的预测因素。在这项研究中,我们基于古代神经网络(Reset)架构的深度神经网络方法,基于经典机器学习方法,并评估其预测ATRX突变状态的能力,而不需要不同的肿瘤分割步骤。我们发现Reset50(50层)架构,预先训练的想象数据是最佳的性能模型,实现了测试集的精度为0.91(切片的分类,也没有肿瘤,ATRX突变或突变)。在35例测试组中得分。基于其突变状态,SVM分类器实现了0.63,用于区分从测试患者的Flair信号异常区域。我们报告了一种减轻了广泛预处理的方法,并作为深度神经网络架构可用于预测来自常规医学图像的分子生物标志物的概念证明。

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