Harris Robert J, Cloughesy Timothy F, Hardy Anthony J, Liau Linda M, Pope Whitney B, Nghiemphu Phioanh L, Lai Albert, Ellingson Benjamin M
UCLA Brain Tumor Imaging Laboratory (BTIL), Department of Radiological Sciences, David Geffen School of Medicine, University of California Los Angeles, 924 Westwood Blvd., Suite 615, Los Angeles, CA, 90024, USA.
J Neurooncol. 2015 May;122(3):497-505. doi: 10.1007/s11060-015-1755-8. Epub 2015 Mar 15.
Bevacizumab is a therapeutic drug used in treatment of recurrent glioblastoma to inhibit angiogenesis. Treatment response is often monitored through the use of perfusion MRI measures of cerebral blood volume, flow, and other pharmacokinetic parameters; however, most methods for deriving these perfusion parameters can produce errors depending on bolus kinetics. Recently, a number of new methods have been developed to overcome these challenges. In the current study we examine cerebral blood volume and blood flow characteristics in 45 recurrent glioblastoma patients before and after treatment with bevacizumab. Perfusion MRI data was processed using a standard single value decomposition (SVD) technique, two block-circulant SVD techniques, and a Bayesian estimation technique. A proportional hazards model showed that patients with a large decrease in relative blood volume (RBV) after treatment had extended overall survival (P = 0.0048). Patients with large pre-treatment relative blood flow (RBF) showed extended progression-free survival (P = 0.0216) and overall survival (P = 0.0112), and patients with a large decrease in RBF following treatment showed extended overall survival (P = 0.0049). These results provide evidence that blood volume and blood flow measurements can be used as biomarkers in patients treated with bevacizumab.
贝伐单抗是一种用于治疗复发性胶质母细胞瘤以抑制血管生成的治疗药物。治疗反应通常通过使用灌注MRI测量脑血容量、血流及其他药代动力学参数来监测;然而,大多数用于推导这些灌注参数的方法可能会因团注动力学而产生误差。最近,已开发出一些新方法来克服这些挑战。在本研究中,我们检测了45例复发性胶质母细胞瘤患者在接受贝伐单抗治疗前后的脑血容量和血流特征。灌注MRI数据使用标准单值分解(SVD)技术、两种块循环SVD技术和一种贝叶斯估计技术进行处理。比例风险模型显示,治疗后相对血容量(RBV)大幅下降的患者总生存期延长(P = 0.0048)。治疗前相对血流(RBF)高的患者无进展生存期延长(P = 0.0216)和总生存期延长(P = 0.0112),且治疗后RBF大幅下降的患者总生存期延长(P = 0.0049)。这些结果提供了证据,表明血容量和血流测量可作为接受贝伐单抗治疗患者的生物标志物。