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首页> 外文期刊>Journal of magnetic resonance imaging: JMRI >Correlation of dynamic contrast enhancement MRI parameters with microvessel density and VEGF for assessment of angiogenesis in breast cancer.
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Correlation of dynamic contrast enhancement MRI parameters with microvessel density and VEGF for assessment of angiogenesis in breast cancer.

机译:动态对比增强MRI参数与微血管密度和VEGF的相关性,以评估乳腺癌中的血管生成。

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PURPOSE: To investigate the association between parameters obtained from dynamic contrast enhanced MRI (DCE-MRI) of breast cancer using different analysis approaches, as well as their correlation with angiogenesis biomarkers (vascular endothelial growth factor and vessel density). MATERIALS AND METHODS: DCE-MRI results were obtained from 105 patients with breast cancer (108 lesions). Three analysis methods were applied: 1) whole tumor analysis, 2) regional hot-spot analysis, and 3) intratumor pixel-by-pixel analysis. Early enhancement intensities and fitted pharmacokinetic parameters were studied. Paraffin blocks of 71 surgically resected specimens were analyzed by immunohistochemical staining to measure microvessel counts (with CD31) and vascular endothelial growth factor (VEGF) expression levels. RESULTS: MRI parameters obtained from the three analysis methods showed significant correlations (P < 0.0001), but a substantial dispersion from the linear regression line was noted (r = 0.72-0.97). The entire region of interest (ROI) vs. pixel population analyses had a significantly higher association compared to the entire ROI vs. hot-spot analyses. Cancer specimens with high VEGF expression had significantly higher CD31 microvessel densities than did specimens with low VEGF levels (P < 0.005). No significant association was found between MRI parameters obtained from the three analysis strategies and IHC based measurements of angiogenesis. CONCLUSION: A consistent analysis strategy was important in the DCE-MRI study. In this series, none of these strategies yielded results for MRI based quantitation of tumor vascularity that were associated with IHC based measurements. Therefore, different analyses could not account for the lack of association. J. Magn. Reson. Imaging 2003;18:467-477.
机译:目的:研究使用不同分析方法从乳腺癌动态对比增强MRI(DCE-MRI)获得的参数之间的关联,以及它们与血管生成生物标记物(血管内皮生长因子和血管密度)的相关性。材料与方法:DCE-MRI结果来自105例乳腺癌患者(108个病灶)。应用了三种分析方法:1)整个肿瘤分析,2)区域热点分析和3)肿瘤内逐像素分析。研究了早期增强强度和拟合的药代动力学参数。通过免疫组织化学染色分析了71个手术切除标本的石蜡块,以测量微血管计数(带有CD31)和血管内皮生长因子(VEGF)的表达水平。结果:从这三种分析方法获得的MRI参数显示出显着的相关性(P <0.0001),但是注意到线性回归线存在较大的分散性(r = 0.72-0.97)。与整个ROI与热点分析相比,整个感兴趣区域(ROI)与像素总体分析的关联性显着更高。高VEGF表达的癌症标本比低VEGF水平的标本具有更高的CD31微血管密度(P <0.005)。从这三种分析策略获得的MRI参数与基于IHC的血管生成测量之间没有发现显着关联。结论:一致的分析策略在DCE-MRI研究中很重要。在本系列中,这些策略均未产生与基于IHC的测量结果相关的基于MRI的肿瘤血管定量定量结果。因此,不同的分析不能说明缺乏关联。 J.Magn。雷森成像2003; 18:467-477。

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