Puig Josep, Blasco Gerard, Daunis-I-Estadella Josep, Alberich-Bayarri Angel, Essig Marco, Jain Rajan, Remollo Sebastián, Hernández David, Puigdemont Montserrat, Sánchez-González Javier, Mateu Gloria, Wintermark Max, Pedraza Salvador
Research Unit of Diagnostic Imaging Institute (IDI), Department of Radiology [Girona Biomedical Research Institute] IDIBGI, Hospital Universitari Dr Josep Trueta, Av de Francia s/n, 17007, Girona, Spain.
Department of Computer Science, Applied Mathematics and Statistics, University of Girona, Girona, Spain.
Neuroradiology. 2016 Jan;58(1):17-26. doi: 10.1007/s00234-015-1599-0. Epub 2015 Oct 5.
The objective of the study was to determine whether tumor-associated neovascularization on high-resolution gadofosveset-enhanced magnetic resonance angiography (MRA) is a useful biomarker for predicting survival in patients with newly diagnosed glioblastomas.
Before treatment, 35 patients (25 men; mean age, 64 ± 14 years) with glioblastoma underwent MRI including first-pass dynamic susceptibility contrast (DSC) perfusion and post-contrast T1WI sequences with gadobutrol (0.1 mmol/kg) and, 48 h later, high-resolution MRA with gadofosveset (0.03 mmol/kg). Volumes of interest for contrast-enhancing lesion (CEL), non-CEL, and contralateral normal-appearing white matter were obtained, and DSC perfusion and DWI parameters were evaluated. Prognostic factors were assessed by Kaplan-Meier survival and Cox proportional hazards model.
Eighteen (51.42 %) glioblastomas were hypervascular on high-resolution MRA. Hypervascular glioblastomas were associated with higher CEL volume and lower Karnofsky score. Median survival rates for patients with hypovascular and hypervascular glioblastomas treated with surgery, radiotherapy, and chemotherapy were 15 and 9.75 months, respectively (P < 0.001). Tumor-associated neovascularization was the best predictor of survival at 5.25 months (AUC = 0.794, 81.2 % sensitivity, 77.8 % specificity, 76.5 % positive predictive value, 82.4 % negative predictive value) and yielded the highest hazard ratio (P < 0.001).
Tumor-associated neovascularization detected on high-resolution blood-pool-contrast-enhanced MRA of newly diagnosed glioblastoma seems to be a useful biomarker that correlates with worse survival.
本研究的目的是确定高分辨率钆弗塞特增强磁共振血管造影(MRA)上的肿瘤相关新生血管形成是否是预测新诊断胶质母细胞瘤患者生存的有用生物标志物。
治疗前,35例胶质母细胞瘤患者(25例男性;平均年龄64±14岁)接受了MRI检查,包括首过动态对比增强(DSC)灌注和使用钆布醇(0.1 mmol/kg)的对比剂后T1WI序列,48小时后,使用钆弗塞特(0.03 mmol/kg)进行高分辨率MRA检查。获取对比增强病变(CEL)、非CEL和对侧正常白质的感兴趣区,并评估DSC灌注和DWI参数。通过Kaplan-Meier生存分析和Cox比例风险模型评估预后因素。
18例(51.42%)胶质母细胞瘤在高分辨率MRA上表现为高灌注。高灌注胶质母细胞瘤与更高的CEL体积和更低的卡诺夫斯基评分相关。接受手术、放疗和化疗的低灌注和高灌注胶质母细胞瘤患者的中位生存率分别为15个月和9.75个月(P<0.001)。肿瘤相关新生血管形成是5.25个月生存的最佳预测指标(AUC=0.794,敏感性81.2%,特异性77.8%,阳性预测值76.5%,阴性预测值82.4%),并产生最高的风险比(P<0.001)。
在新诊断胶质母细胞瘤的高分辨率血池对比增强MRA上检测到的肿瘤相关新生血管形成似乎是一个与较差生存相关的有用生物标志物。