Survival rate prediction of nasopharyngeal carcinoma patients based on <scp>MRI</scp> and gene expression using a deep neural network
Qihao Zhang, Gang Wu, Qianyu Yang, Ganmian Dai, Tiansheng Li, Pianpian Chen, Jiao Li, Weiyuan Huang
Abstract
Abstract To achieve a better treatment regimen and follow‐up assessment design for intensity‐modulated radiotherapy (IMRT)‐treated nasopharyngeal carcinoma (NPC) patients, an accurate progression‐free survival (PFS) time prediction algorithm is needed. We propose developing a PFS prediction model of NPC patients after IMRT treatment using a deep learning method and comparing that with the traditional texture analysis method. One hundred and fifty‐one NPC patients were included in this retrospective study. T1‐weighted, proton density and dynamic contrast‐enhanced magnetic resonance (MR) images were acquired. The expression level of five genes (HIF‐1α, EGFR, PTEN, Ki‐67, and VEGF) and infection of Epstein–Barr (EB) virus were tested. A residual network was trained to predict PFS from MR images. The output as well as patient characteristics were combined using a linear regression model to provide a final PFS prediction. The prediction accuracy was compared with that of the traditional texture analysis method. A regression model combining the deep learning output with HIF‐1α expression and Epstein–Barr infection provides the best PFS prediction accuracy (Spearman correlation R 2 = 0.53; Harrell's C‐index = 0.82; receiver operative curve [ROC] analysis area under the curve [AUC] = 0.88; log‐rank test hazard ratio [HR] = 8.45), higher than a regression model combining texture analysis with HIF‐1α expression (Spearman correlation R 2 = 0.14; Harrell's C‐index =0.68; ROC analysis AUC = 0.76; log‐rank test HR = 2.85). The deep learning method does not require a manually drawn tumor region of interest. MR image processing using deep learning combined with patient characteristics can provide accurate PFS prediction for nasopharyngeal carcinoma patients and does not rely on specific kernels or tumor regions of interest, which is needed for the texture analysis method.