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抗血管生成治疗的胶质母细胞瘤患者的血管迟滞环和血管结构图谱

Vascular Hysteresis Loops and Vascular Architecture Mapping in Patients with Glioblastoma treated with Antiangiogenic Therapy.

机构信息

Department of Neurosurgery, University of Erlangen-Nürnberg, Erlangen, Germany.

Institute of Medical Radiology, University Clinic of St. Pölten, St. Pölten, Austria.

出版信息

Sci Rep. 2017 Aug 17;7(1):8508. doi: 10.1038/s41598-017-09048-w.

DOI:10.1038/s41598-017-09048-w
PMID:28819189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5561153/
Abstract

In this study, we investigated the variability of vascular hysteresis loop (VHL) shapes and the spatial heterogeneity of neovascularization and microvascular alterations using vascular architecture mapping (VAM) in patients with recurrent glioblastoma during bevacizumab mono-therapy. VAM data were acquired in 13 patients suffering from recurrent glioblastoma prior to and 3 months after bevacizumab treatment onset using a dual contrast agent injections approach as part of routine MRI. Two patients were additionally examined after the first cycle of bevacizumab to check for early treatment response. VHLs were evaluated as biomarker maps of neovascularization activity: microvessel type indicator (MTI) and curvature (Curv) of the VHL-long-axis. Early response to bevacizumab was dominated by reduction of smaller microvasculature (around 10 µm). In the 3-month follow-up, responding tumors additionally showed a reduction in larger microvasculature (>20 µm). VAM biomarker images revealed spatially heterogeneous microvascular alterations during bevacizumab treatment. Responding, non-responding, progressive, and remote-progressive tumor areas were observed. MTI may be useful to predict responding and non-responding tumor regions, and Curv to assess severity of vasogenic edema. Analysis of VHLs in combination with VAM biomarkers may lead to a new perspective on investigating the spatial heterogeneity of neovascularization and microvascular alterations in glioblastoma during antiangiogenic therapy.

摘要

在这项研究中,我们使用血管结构测绘(VAM)研究了复发性胶质母细胞瘤患者在贝伐单抗单药治疗期间血管滞后环(VHL)形状的可变性以及新生血管和微血管改变的空间异质性。VAM 数据是在 13 名复发性胶质母细胞瘤患者中获得的,这些患者在贝伐单抗治疗开始前和 3 个月时使用双重对比剂注射方法进行了常规 MRI 检查。为了检查早期治疗反应,有两名患者在接受贝伐单抗第一个周期后进行了额外检查。VHL 作为新生血管活性的生物标志物图谱进行评估:微血管类型指标(MTI)和 VHL 长轴的曲率(Curv)。贝伐单抗的早期反应主要是较小的微血管减少(约 10μm)。在 3 个月的随访中,反应性肿瘤还显示较大的微血管(>20μm)减少。VAM 生物标志物图像显示在贝伐单抗治疗期间微血管发生了空间异质性改变。观察到了反应性、非反应性、进行性和远程进行性肿瘤区域。MTI 可能有助于预测反应性和非反应性肿瘤区域,而 Curv 可用于评估血管源性水肿的严重程度。对 VHL 的分析结合 VAM 生物标志物可能为研究抗血管生成治疗期间胶质母细胞瘤新生血管和微血管改变的空间异质性提供新视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03aa/5561153/4b6a43ecce24/41598_2017_9048_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03aa/5561153/3a31957b2f02/41598_2017_9048_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03aa/5561153/ddd8ec70ca0c/41598_2017_9048_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03aa/5561153/71985f4dcdf5/41598_2017_9048_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03aa/5561153/a2b88f8b8908/41598_2017_9048_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03aa/5561153/4b6a43ecce24/41598_2017_9048_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03aa/5561153/3a31957b2f02/41598_2017_9048_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03aa/5561153/ddd8ec70ca0c/41598_2017_9048_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03aa/5561153/71985f4dcdf5/41598_2017_9048_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03aa/5561153/a2b88f8b8908/41598_2017_9048_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03aa/5561153/4b6a43ecce24/41598_2017_9048_Fig5_HTML.jpg

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