Linguraru Marius George, Yao Jianhua, Gautam Rabindra, Peterson James, Li Zhixi, Linehan W Marston, Summers Ronald M
Diagnostic Radiology Department, Clinical Center, National Institutes of Health, Bethesda, MD, USA.
Pattern Recognit. 2009 Jun 1;42(6):1149-1161. doi: 10.1016/j.patcog.2008.09.018.
Kidney cancer occurs in both a hereditary (inherited) and sporadic (non-inherited) form. It is estimated that almost a quarter of a million people in the USA are living with kidney cancer and their number increases with 51,000 diagnosed with the disease every year. In clinical practice, the response to treatment is monitored by manual measurements of tumor size, which are 2D, do not reflect the 3D geometry and enhancement of tumors, and show high intra- and inter-operator variability. We propose a computer-assisted radiology tool to assess renal tumors in contrast-enhanced CT for the management of tumor diagnoses and responses to new treatments. The algorithm employs anisotropic diffusion (for smoothing), a combination of fast-marching and geodesic level-sets (for segmentation), and a novel statistical refinement step to adapt to the shape of the lesions. It also quantifies the 3D size, volume and enhancement of the lesion and allows serial management over time. Tumors are robustly segmented and the comparison between manual and semi-automated quantifications shows disparity within the limits of inter-observer variability. The analysis of lesion enhancement for tumor classification shows great separation between cysts, von Hippel-Lindau syndrome lesions and hereditary papillary renal carcinomas (HPRC) with p-values inferior to 0.004. The results on temporal evaluation of tumors from serial scans illustrate the potential of the method to become an important tool for disease monitoring, drug trials and noninvasive clinical surveillance.
肾癌以遗传性(遗传)和散发性(非遗传)两种形式出现。据估计,美国有近25万人患有肾癌,且每年新增51000例确诊病例。在临床实践中,通过手动测量肿瘤大小来监测治疗反应,这种测量是二维的,无法反映肿瘤的三维几何形状和强化情况,并且在操作者内部和操作者之间存在很大差异。我们提出一种计算机辅助放射学工具,用于在对比增强CT中评估肾肿瘤,以管理肿瘤诊断和对新治疗的反应。该算法采用各向异性扩散(用于平滑)、快速行进和测地线水平集的组合(用于分割)以及一个新颖的统计细化步骤来适应病变的形状。它还可以量化病变的三维大小、体积和强化情况,并允许进行长期的连续管理。肿瘤被稳健地分割,手动和半自动量化之间的比较显示出在观察者间差异范围内的差异。对肿瘤分类的病变强化分析显示,囊肿、冯·希佩尔-林道综合征病变和遗传性乳头状肾癌(HPRC)之间有很大的区分,p值小于0.004。连续扫描对肿瘤进行时间评估的结果表明,该方法有可能成为疾病监测、药物试验和无创临床监测的重要工具。