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Dynamic contrast-enhanced magnetic resonance imaging of the metastatic potential of tumors: A preclinical study of cervical carcinoma and melanoma xenografts

机译:肿瘤转移潜力的动态对比增强磁共振成像:宫颈癌和黑色素瘤异种移植物的临床前研究

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Background. Gadolinium diethylene-triamine penta-acetic acid (Gd-DTPA)-based dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) has been suggested to be a useful non-invasive method for providing biomarkers for personalized cancer treatment. In this preclinical study, we investigated whether Gd-DTPA-based DCE-MRI may have the potential to differentiate between poorly and highly metastatic tumors. Material and methods. CK-160 cervical carcinoma and V-27 melanoma xenografts were used as tumor models. Fifty-six tumors were imaged, and parametric images of Ktrans (the volume transfer constant of Gd-DTPA) and ve (the fractional distribution volume of Gd-DTPA) were produced by pharmacokinetic analysis of the DCE-MRI series. The host mice were examined for lymph node metastases immediately after the DCE-MRI. Results. Highly metastatic tumors showed lower values for median Ktrans than poorly metastatic tumors (p = 0.00033, CK-160; p 0.00001, V-27). Median ve was lower for highly than for poorly metastatic V-27 tumors (p = 0.047), but did not differ significantly between metastatic and non-metastatic CK-160 tumors (p 0.05). Conclusion. This study supports the clinical attempts to establish DCE-MRI as a method for providing biomarkers for tumor aggressiveness and suggests that tumors showing low Ktrans and low ve values may have high probability of lymphogenous metastatic dissemination.
机译:背景。 d二乙三胺五乙酸(Gd-DTPA)为基础的动态对比增强磁共振成像(DCE-MRI)已被建议是一种有用的非侵入性方法,可为个性化癌症治疗提供生物标志物。在这项临床前研究中,我们调查了基于Gd-DTPA的DCE-MRI是否有可能区分低转移性肿瘤和高转移性肿瘤。材料与方法。 CK-160宫颈癌和V-27黑色素瘤异种移植物用作肿瘤模型。对56个肿瘤进行成像,并通过DCE-MRI系列的药代动力学分析生成Ktrans(Gd-DTPA的体积转移常数)和ve(Gd-DTPA的分数分布体积)的参数化图像。 DCE-MRI后立即检查宿主小鼠的淋巴结转移情况。结果。高度转移性肿瘤的中位Ktrans值低于转移性较差的肿瘤(p = 0.00033,CK-160; p <0.00001,V-27)。高中位数ve低于转移性差的V-27肿瘤(p = 0.047),但转移性和非转移性CK-160肿瘤之间无显着差异(p> 0.05)。结论。这项研究支持建立DCE-MRI作为为肿瘤侵袭性提供生物标志物的方法的临床尝试,并表明显示出低Ktrans和低ve值的肿瘤可能具有较高的淋巴结转移转移可能性。

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