Radiomic analysis of imaging heterogeneity in tumours and the surrounding parenchyma based on unsupervised decomposition of DCE-MRI for predicting molecular subtypes of breast cancer

被引:67
|
作者
Fan, Ming [1 ]
Zhang, Peng [1 ]
Wang, Yue [2 ]
Peng, Weijun [3 ]
Wang, Shiwei [4 ]
Gao, Xin [5 ]
Xu, Maosheng [4 ]
Li, Lihua [1 ]
机构
[1] Hangzhou Dianzi Univ, Inst Biomed Engn & Instrumentat, Hangzhou, Zhejiang, Peoples R China
[2] Virginia Polytech Inst & State Univ, Dept Elect & Comp Engn, Arlington, VA 22203 USA
[3] Fudan Univ, Dept Radiol, Shanghai Canc Ctr, Shanghai, Peoples R China
[4] Zhejiang Chinese Med Univ, Affiliated Hosp 1, Dept Radiol, Hangzhou, Zhejiang, Peoples R China
[5] KAUST, CBRC, Comp Elect & Math Sci & Engn Div CEMSE, Thuwal 239556900, Saudi Arabia
基金
中国国家自然科学基金;
关键词
Breast neoplasms; Magnetic resonance imaging; Diagnostic imaging; NEOADJUVANT CHEMOTHERAPY; ENHANCEMENT; PHENOTYPES; DECONVOLUTION; PARAMETERS; FEATURES;
D O I
10.1007/s00330-018-5891-3
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
ObjectivesThis study aimed to predict the molecular subtypes of breast cancer via intratumoural and peritumoural radiomic analysis with subregion identification based on the decomposition of contrast-enhanced magnetic resonance imaging (DCE-MRI).MethodsThe study included 211 women with histopathologically confirmed breast cancer. We utilised a completely unsupervised convex analysis of mixtures (CAM) method by unmixing dynamic imaging series from heterogeneous tissues. Each tumour and the surrounding parenchyma were thus decomposed into multiple subregions, representing different vascular characterisations, from which radiomic features were extracted. A random forest model was trained and tested using a leave-one-out cross-validation (LOOCV) method to predict breast cancer subtypes. The predictive models from tumoural and peritumoural subregions were fused for classification.ResultsTumour and peritumour DCE-MR images were decomposed into three compartments, representing plasma input, fast-flow kinetics, and slow-flow kinetics. The tumour subregion related to fast-flow kinetics showed the best performance among the subregions for differentiating between patients with four molecular subtypes (area under the receiver operating characteristic curve (AUC)=0.832), exhibiting an AUC value significantly (p<0.0001) higher than that obtained with the entire tumour (AUC=0.719). When the tumour- and parenchyma-based predictive models were fused, the performance, measured as the AUC, increased to 0.897; this value was significantly higher than that obtained with other tumour partition methods.ConclusionsRadiomic analysis of intratumoural and peritumoural heterogeneity based on the decomposition of image time-series signals has the potential to more accurately identify tumour kinetic features and serve as a valuable clinical marker to enhance the prediction of breast cancer subtypes.Key Points center dot Decomposition of image time-series signals has the potential to more accurately identify tumour kinetic features.center dot Fusion of intratumoural- and peritumoural-based predictive models improves the prediction of breast cancer subtypes.
引用
收藏
页码:4456 / 4467
页数:12
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