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High-grade glioma before and after treatment with radiation and Avastin: Initial observations

机译:放疗和阿瓦斯汀治疗前后的高度神经胶质瘤:初步观察

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We evaluate the effects of adjuvant treatment with the angiogenesis inhibitor Avastin (bevacizumab) on pathological tissue specimens of high-grade glioma. Tissue from five patients before and after treatment with Avastin was subjected to histological evaluation and compared to four control cases of glioma before and after similar treatment protocols not including bevacizumab. Clinical and radiographic data were reviewed. Histological analysis focused on microvessel density and vascular morphology, and expression patterns of vascular endothe-lial growth factor-A (VEGF-A) and the hematopoietic stem cell, mesenchymal, and cell motility markers CD34, smooth muscle actin, D2-40, and fascin. All patients with a decrease in microvessel density had a radiographic response, whereas no response was seen in the patients with increased microvessel density. Vascular morphology showed apparent "normalization" after Avastin treatment in two cases, with thin-walled and evenly distributed vessels. VEGF-A expression in tumor cells was increased in two cases and decreased in three and did not correlate with treatment response. There was a trend toward a relative increase of CD34, smooth muscle actin, D2-40, and fascin immunostaining following treatment with Avastin. Specimens from four patients with recurrent malignant gliomas before and after adjuvant treatment (not including bevacizumab) had features dissimilar from our study cases. We conclude that a change in vascular morphology can be observed following anti-angiogenic treatment. There seems to be no correlation between VEGF-A expression and clinical parameters. While the phenomena we describe may not be specific to Avastin, they demonstrate the potential of tissue-based analysis for the discovery of clinically relevant treatment response biomarkers.
机译:我们评估血管生成抑制剂阿瓦斯汀(贝伐单抗)对高级别神经胶质瘤病理组织标本的辅助治疗效果。对5名接受Avastin治疗前后的患者的组织进行组织学评估,并将其与4例神经胶质瘤的对照病例进行比较(包括贝伐单抗),治疗前后相似。回顾了临床和影像学数据。组织学分析集中于微血管密度和血管形态,以及血管内皮生长因子-A(VEGF-A)和造血干细胞,间充质和细胞运动性标记CD34,平滑肌肌动蛋白,D2-40和fascin。所有微血管密度降低的患者均发生放射线照相反应,而微血管密度增加的患者未见反应。 Avastin治疗后的2例患者血管形态显示明显的“正常化”,血管薄壁且分布均匀。 VEGF-A在肿瘤细胞中的表达在2例中增加,在3例中减少,并且与治疗反应无​​关。用阿瓦斯汀治疗后,CD34,平滑肌肌动蛋白,D2-40和fascin免疫染色有相对增加的趋势。在辅助治疗前后(不包括贝伐单抗)的四名复发性恶性神经胶质瘤患者的标本特征与我们的研究病例不同。我们得出的结论是,抗血管生成治疗后可以观察到血管形态的变化。 VEGF-A表达与临床参数之间似乎没有相关性。尽管我们描述的现象可能不是Avastin特有的,但它们证明了基于组织的分析在发现临床相关治疗反应生物标志物方面的潜力。

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