Non-invasive prediction of microsatellite instability in colorectal cancer by a genetic algorithm-enhanced artificial neural network-based CT radiomics signature

被引:17
作者
Chen, Xiaobo [1 ,2 ,3 ]
He, Lan [1 ,2 ]
Li, Qingshu [4 ]
Liu, Liu [5 ]
Li, Suyun [1 ,2 ,6 ]
Zhang, Yuan [1 ,2 ,3 ]
Liu, Zaiyi [1 ,2 ]
Huang, Yanqi [1 ,2 ]
Mao, Yun [1 ,5 ]
Chen, Xin [7 ]
机构
[1] Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Dept Radiol, 106 Zhongshan Er Rd, Guangzhou 510080, Peoples R China
[2] Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Guangdong Prov Key Lab Artificial Intelligence Me, Guangzhou 510080, Peoples R China
[3] Southern Med Univ, Sch Clin Med 2, Guangzhou 510515, Peoples R China
[4] Chongqing Med Univ, Coll Basic Med, Dept Pathol, Chongqing 400016, Peoples R China
[5] Chongqing Med Univ, Dept Radiol, Affiliated Hosp 1, Chongqing 400016, Peoples R China
[6] South China Univ Technol, Sch Med, Guangzhou 510006, Peoples R China
[7] South China Univ Technol, Guangzhou Peoples Hosp 1, Sch Med, Dept Radiol, 1 Panfu Rd, Guangzhou 510180, Peoples R China
关键词
Colorectal neoplasms; Microsatellite instability; Neural networks; Survival analysis; HETEROGENEITY;
D O I
10.1007/s00330-022-08954-6
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
Objective The stratification of microsatellite instability (MSI) status assists clinicians in making treatment decisions for colorectal cancer (CRC) patients. This study aimed to establish a CT-based radiomics signature to predict MSI status in patients with CRC. Methods A total of 837 CRC patients who underwent preoperative enhanced CT and had available MSI status data were recruited from two hospitals. Radiomics features were extracted from segmented tumours, and a series of data balancing and feature selection strategies were used to select MSI-related features. Finally, an MSI-related radiomics signature was constructed using a genetic algorithm-enhanced artificial neural network model. Combined and clinical models were constructed using multivariate logistic regression analyses by integrating the clinical factors with or without the signature. A Kaplan-Meier survival analysis was conducted to explore the prognostic information of the signature in patients with CRC. Results Ten features were selected to construct a signature which showed robust performance in both the internal and external validation cohorts, with areas under the curves (AUC) of 0.788 and 0.775, respectively. The performance of the signature was comparable to that of the combined model (AUCs of 0.777 and 0.767, respectively) and it outperformed the clinical model constituting age and tumour location (AUCs of 0.768 and 0.623, respectively). Survival analysis demonstrated that the signature could stratify patients with stage II CRC according to prognosis (HR: 0.402, p = 0.029). Conclusions This study built a robust radiomics signature for identifying the MSI status of CRC patients, which may assist individualised treatment decisions.
引用
收藏
页码:11 / 22
页数:12
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