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动态钆布醇增强磁共振成像在小鼠异种移植模型中可预测对抗血管生成治疗而非抗增殖治疗的早期反应。

Dynamic gadobutrol-enhanced MRI predicts early response to antivascular but not to antiproliferation therapy in a mouse xenograft model.

作者信息

Dassler Katrin, Scholle Frank-Detlef, Schütz Gunnar

机构信息

MR & CT Contrast Media Research, Bayer Pharma AG, Berlin, Germany.

出版信息

Magn Reson Med. 2014 May;71(5):1826-33. doi: 10.1002/mrm.24815. Epub 2013 Jun 10.

DOI:10.1002/mrm.24815
PMID:23754607
Abstract

PURPOSE

Dynamic contrast-enhanced magnetic resonance imaging has been described as a method to assess tumor vascularity and, therefore, is discussed as a noninvasive biomarker for drug response prediction in tumor therapies. Because antiangiogenic and antiproliferative drugs are frequently combined for therapy, the aim was to investigate (1) the early response predictability and (2) the extent to which these therapy types influence dynamic contrast-enhanced magnetic resonance imaging with gadobutrol soon after therapy initiation.

METHODS

Mice bearing a KPL-4 tumor were treated with either bevacizumab as an antiangiogenic drug or trastuzumab as a cytotoxic anti-tumor drug. The gadobutrol-contrast agent exposure of the tumor was recorded before and at several time points after therapy initiation to examine the response prediction by dynamic contrast-enhanced magnetic resonance imaging.

RESULTS

Both therapies resulted in significant tumor growth attenuation over 30 days of therapy, but the individual response to each therapy was different. Specifically, bevacizumab affected the dynamic gadobutrol-enhanced MRI-derived area under the curve at early time points (≤8 days), while trastuzumab did not.

CONCLUSION

The area under the curve obtained from dynamic gadobutrol-enhanced MRI predicted early tumor response to the antiangiogenic drug bevacizumab, but not to the anti-tumor cell drug trastuzumab. This indicates that the area under the curve may be useful for assessing early antiangiogenic but not antiproliferative drug effects.

摘要

目的

动态对比增强磁共振成像已被描述为一种评估肿瘤血管生成的方法,因此被讨论作为肿瘤治疗中药物反应预测的一种非侵入性生物标志物。由于抗血管生成和抗增殖药物经常联合用于治疗,本研究旨在探讨:(1)早期反应的可预测性;(2)这些治疗类型在治疗开始后不久对钆布醇动态对比增强磁共振成像的影响程度。

方法

用抗血管生成药物贝伐单抗或细胞毒性抗肿瘤药物曲妥珠单抗治疗携带KPL - 4肿瘤的小鼠。在治疗开始前及开始后的几个时间点记录肿瘤的钆布醇造影剂暴露情况,以通过动态对比增强磁共振成像检查反应预测情况。

结果

两种治疗在30天的治疗期内均导致肿瘤生长显著减缓,但每种治疗的个体反应不同。具体而言,贝伐单抗在早期时间点(≤8天)影响了动态钆布醇增强磁共振成像衍生的曲线下面积,而曲妥珠单抗则没有。

结论

动态钆布醇增强磁共振成像获得的曲线下面积可预测肿瘤对抗血管生成药物贝伐单抗的早期反应,但不能预测对抗肿瘤细胞药物曲妥珠单抗的反应。这表明曲线下面积可能有助于评估早期抗血管生成药物的效果,但不能评估抗增殖药物的效果。

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