Multilevel analysis of spatiotemporal association features for differentiation of tumor enhancement patterns in breast DCE-MRI

被引:50
|
作者
Lee, Sang Ho [2 ,3 ]
Kim, Jong Hyo [1 ]
Cho, Nariya [4 ]
Park, Jeong Seon [4 ]
Yang, Zepa [5 ]
Jung, Yun Sub [6 ]
Moon, Woo Kyung [1 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Radiol, Seoul 110744, South Korea
[2] Seoul Natl Univ, Coll Med, Interdisciplinary Program Radiat Appl Life Sci, Seoul 110744, South Korea
[3] Seoul Natl Univ, Med Res Ctr, Inst Radiat Med, Seoul 110744, South Korea
[4] Seoul Natl Univ Hosp, Dept Radiol, Seoul 110744, South Korea
[5] Seoul Natl Univ, Coll Med, Dept Biomed Sci, Seoul 110744, South Korea
[6] Seoul Natl Univ, Coll Med, Interdisciplinary Program Radiat Appl Life Sci, Seoul 110744, South Korea
关键词
breast dynamic contrast-enhanced MRI; computer-aided diagnosis; spatiotemporal association; feature extraction; classification; 3D moment invariants; support vector machines; tumor characterization; AIDED-DIAGNOSIS CAD; HIGH FAMILIAL RISK; SPATIAL-RESOLUTION; NONRIGID REGISTRATION; CANCER; MAMMOGRAPHY; LESIONS; CLASSIFICATION; WOMEN; CURVES;
D O I
10.1118/1.3446799
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
Purpose: Analyzing spatiotemporal enhancement patterns is an important task for the differential diagnosis of breast tumors in dynamic contrast-enhanced MRI (DCE-MRI), and yet remains challenging because of complexities in analyzing the time-series of three-dimensional image data. The authors propose a novel approach to breast MRI computer-aided diagnosis (CAD) using a multi-level analysis of spatiotemporal association features for tumor enhancement patterns in DCE-MRI. Methods: A database of 171 cases consisting of 111 malignant and 60 benign tumors was used. Time-series contrast-enhanced MR images were obtained from two different types of MR scanners and protocols. The images were first registered for motion compensation, and then tumor regions were segmented using a fuzzy c-means clustering-based method. Spatiotemporal associations of tumor enhancement patterns were analyzed at three levels: Mapping of pixelwise kinetic features within a tumor, extraction of spatial association features from kinetic feature maps, and extraction of kinetic association features at the spatial feature level. A total of 84 initial features were extracted. Predictable values of these features were evaluated with an area under the ROC curve, and were compared between the spatiotemporal association features and a subset of simple form features which do not reflect spatiotemporal association. 'Several optimized feature sets were identified among the spatiotemporal association feature group or among the simple feature group based on a feature ranking criterion using a support vector machine based recursive feature elimination algorithm. A least-squares support vector machine (LS-SVM) classifier was used for tumor differentiation and the performances were evaluated using a leave-one-out testing. Results: Predictable values of the extracted single features ranged in 0.52-0.75. By applying multilevel analysis strategy, the spatiotemporal association features became more informative in predicting tumor malignancy, which was shown by a statistical testing in ten spatiotemporal association features. By using a LS-SVM classifier with the optimized second and third level feature set, the CAD scheme showed A(z) of 0.88 in classification of malignant and benign tumors. When this performance was compared to the same LS-SVM classifier with simple form features which do not reflect spatiotemporal association, there was a statistically significant difference (0.88 vs 0.79, p<0.05), suggesting that the multilevel analysis strategy yields a significant performance improvement. Conclusions: The results suggest that the multilevel analysis strategy characterizes the complex tumor enhancement patterns effectively with the spatiotemporal association features, which in turn leads to an improved tumor differentiation. The proposed CAD scheme has a potential for improving diagnostic performance in breast DCE-MRI. (C) 2010 American Association of Physicists in Medicine. [DOI: 10.1118/1.3446799]
引用
收藏
页码:3940 / 3956
页数:17
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