Development and validation of MRI-based radiomics signatures models for prediction of disease-free survival and overall survival in patients with esophageal squamous cell carcinoma

被引:23
作者
Chu, Funing [1 ,2 ]
Liu, Yun [3 ]
Liu, Qiuping [4 ]
Li, Weijia [5 ]
Jia, Zhengyan [1 ,2 ]
Wang, Chenglong [3 ]
Wang, Zhaoqi [1 ,2 ]
Lu, Shuang [1 ,2 ]
Li, Ping [1 ,2 ]
Zhang, Yuanli [1 ,2 ]
Liao, Yubo [1 ,2 ]
Xu, Mingzhe [1 ,2 ]
Yao, Xiaoqiang [1 ,2 ]
Wang, Shuting [1 ,2 ]
Liu, Cuicui [1 ,2 ]
Zhang, Hongkai [1 ,2 ]
Wang, Shaoyu [6 ]
Yan, Xu [7 ]
Kamel, Ihab R. [8 ]
Sun, Haibo [2 ,9 ]
Yang, Guang [3 ]
Zhang, Yudong [4 ]
Qu, Jinrong [1 ,2 ]
机构
[1] Zhengzhou Univ, Dept Radiol, Affiliated Canc Hosp, 127 Dongming Rd, Zhengzhou 450008, Henan, Peoples R China
[2] Henan Canc Hosp, 127 Dongming Rd, Zhengzhou 450008, Henan, Peoples R China
[3] East China Normal Univ, Shanghai Key Lab Magnet Resonance, Shanghai 200062, Peoples R China
[4] Nanjing Med Univ, Dept Radiol, Affiliated Hosp 1, 300 Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
[5] Henan Prov Inst Med Equipment Testing, Zhengzhou 450000, Henan, Peoples R China
[6] Siemens Healthineers, MR Sci Mkt, Xian 710065, Peoples R China
[7] Siemens Healthineers, MR Sci Mkt, Shanghai 201318, Peoples R China
[8] Johns Hopkins Univ, Dept Radiol, Sch Med, Baltimore, MD 21205 USA
[9] Zhengzhou Univ, Dept Thorac Surg, Affiliated Canc Hosp, Zhengzhou 450008, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Esophageal neoplasms; Neoplasm staging; Magnetic resonance imaging; CANCER;
D O I
10.1007/s00330-022-08776-6
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objectives To develop and validate an optimal model based on the 1-mm-isotropic-3D contrast-enhanced StarVIBE MRI sequence combined with clinical risk factors for predicting survival in patients with esophageal squamous cell carcinoma (ESCC). Methods Patients with ESCC at our institution from 2015 to 2017 participated in this retrospective study based on prospectively acquired data, and were randomly assigned to training and validation groups at a ratio of 7:3. Random survival forest (RSF) and variable hunting methods were used to screen for radiomics features and LASSO-Cox regression analysis was used to build three models, including clinical only, radiomics only and combined clinical and radiomics models, which were evaluated by concordance index (CI) and calibration curve. Nomograms and decision curve analysis (DCA) were used to display intuitive prediction information. Results Seven radiomics features were selected from 434 patients, combined with clinical features that were statistically significant to construct the predictive models of disease-free survival (DFS) and overall survival (OS). The combined model showed the highest performance in both training and validation groups for predicting DFS ([CI], 0.714, 0.729) and OS ([CI], 0.730, 0.712). DCA showed that the net benefit of the combined model and of the clinical model is significantly greater than that of the radiomics model alone at different threshold probabilities. Conclusions We demonstrated that a combined predictive model based on MR Rad-S and clinical risk factors had better predictive efficacy than the radiomics models alone for patients with ESCC.
引用
收藏
页码:5930 / 5942
页数:13
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