Li Lin, Wang Kai, Sun Xilin, Wang Kezheng, Sun Yingying, Zhang Guangfeng, Shen Baozhong
Department of Radiology, Fourth Hospital of Harbin Medical University, Harbin, Heilongjiang, China (mainland).
Molecular Imaging Center, Harbin Medical University, Harbin, Heilongjiang, China (mainland).
Med Sci Monit. 2015 Feb 1;21:376-82. doi: 10.12659/MSM.892534.
Breast cancer is the most common malignancy and the leading cause of cancer death in women worldwide; however, early diagnosis has been difficult due to its complex pathological structure. This study evaluated the value of morphological examination in conjunction with dynamic contrast-enhanced MRI (DCE-MRI) for more precise diagnosis of breast cancer, as well as their correlation with angiogenesis and proliferation biomarkers.
MATERIAL/METHODS: DCE-MRI parameters (including Ktrans: volume transfer coefficient reflecting vascular permeability, Kep: flux rate constant, Ve: extracellular volume ratio reflecting vascular permeability, and ADC: apparent diffusion coefficient) were obtained from 124 patients with breast cancer (124 lesions). Microvessel density (MVD) was evaluated by the immunohistochemical analysis of tumor vessels for CD31 and CD105 expression. The proliferation was assessed by analyzing Ki67.
Ktrans values were in the order of: malignant lesions>benign lesions>normal glands. Similar results were observed for Kep. The opposite changes were seen with Ve. Ktrans and Kep values were significantly higher in invasive ductal carcinoma (IDC) and ductal carcinoma in situ (DCIS) than in mammary ductal dysplasia (MDD; ANOVA followed by Dunnett's test). In sharp contrast, ADC values were lower in IDC and DCIS than in MDD, and Ve was not significantly different among the three groups. The data from MIP (maximum intensity projection) showed that benign breast lesions had no or only one blood vessel, whereas malignant lesions had two or more blood vessels. In addition, expression of CD105 and Ki67, the commonly recognized markers for angiogenesis and proliferation, respectively, were closely correlated with MRI parameters as revealed by Pearson analysis.
Determination of Ktrans, Kep and ADC values permits estimation of tumor angiogenesis and proliferation in breast cancer and DCE-MRI parameters can be used as imaging biomarkers to predict patient prognosis and the biologic aggressiveness of the tumor.
乳腺癌是全球女性中最常见的恶性肿瘤,也是癌症死亡的主要原因;然而,由于其复杂的病理结构,早期诊断一直很困难。本研究评估了形态学检查联合动态对比增强磁共振成像(DCE-MRI)对乳腺癌更精确诊断的价值,以及它们与血管生成和增殖生物标志物的相关性。
材料/方法:从124例乳腺癌患者(124个病灶)中获取DCE-MRI参数(包括Ktrans:反映血管通透性的容积转运系数、Kep:流速常数、Ve:反映血管通透性的细胞外容积比、ADC:表观扩散系数)。通过对肿瘤血管进行CD31和CD105表达的免疫组织化学分析来评估微血管密度(MVD)。通过分析Ki67评估增殖情况。
Ktrans值的顺序为:恶性病灶>良性病灶>正常腺体。Kep也观察到类似结果。Ve则呈现相反变化。浸润性导管癌(IDC)和原位导管癌(DCIS)的Ktrans和Kep值显著高于乳腺导管发育异常(MDD;方差分析后进行Dunnett检验)。与之形成鲜明对比的是,IDC和DCIS的ADC值低于MDD,且三组之间Ve无显著差异。最大强度投影(MIP)数据显示,良性乳腺病灶无血管或仅有一条血管,而恶性病灶有两条或更多血管。此外,Pearson分析显示,分别作为血管生成和增殖的常用标志物CD105和Ki67的表达与MRI参数密切相关。
测定Ktrans、Kep和ADC值可评估乳腺癌中的肿瘤血管生成和增殖情况,DCE-MRI参数可作为影像学生物标志物来预测患者预后和肿瘤的生物学侵袭性。