Differentiation between vasogenic-edema versus tumor-infiltrative area in patients with glioblastoma during bevacizumab therapy: A longitudinal MRI study

被引:53
作者
Artzi, Moran [1 ,2 ]
Bokstein, Felix [3 ]
Blumenthal, Deborah T. [3 ]
Aizenstein, Orna [1 ]
Liberman, Gilad [1 ,4 ]
Corn, Benjamin W. [1 ,5 ]
Ben Bashat, Dafna [1 ,2 ,6 ]
机构
[1] Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Funct Brain Ctr, IL-69978 Tel Aviv, Israel
[2] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
[3] Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Neurooncol Serv, IL-69978 Tel Aviv, Israel
[4] Bar Ilan Univ, Gonda Multidisciplinary Brain Res Ctr, Ramat Gan, Israel
[5] Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Inst Radiotherapy, IL-69978 Tel Aviv, Israel
[6] Tel Aviv Univ, Sagol Sch Neurosci, IL-69978 Tel Aviv, Israel
关键词
Glioblastoma; Bevacizumab; Vasogenic-edema; Tumor infiltrative areas; RANO criteria; MAGNETIC-RESONANCE SPECTROSCOPY; HIGH-GRADE GLIOMAS; RECURRENT GLIOBLASTOMA; PERITUMORAL EDEMA; BRAIN-TUMORS; SEGMENTATION; PROGRESSION; PERFUSION; CLASSIFICATION; SUSCEPTIBILITY;
D O I
10.1016/j.ejrad.2014.03.026
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background: Treatment with bevacizumab is associated with substantial radiologic response in patients with glioblastoma ( GB). However, following this initial response, changes in T2-weighted MRI signal may develop, suggesting an infiltrative pattern of tumor progression. The aim of this study was to differentiate between vasogenic-edema versus tumor-infiltrative area in GB patients. Methods and materials: Fourteen patients with GB were longitudinally scanned, before and during intravenous bevacizumab therapy (5110 mg/kg every 2-weeks). A total of 40 MR scans including conventional, diffusion, dynamic susceptibility contrast, dynamic contrast enhancement imaging, and MR-spectroscopy (MRS) were analyzed. Classification of non-enhancing fluid-attenuation-inversion-recovery (FLAIR) area was performed based on mean diffusivity, cerebral blood volume and flow maps, and further characterized using multiple MRI parameters. Results: The non-enhancing FLAIR lesion area was classified into: vasogenic-edema, characterized by reduced perfusion and increased FLAIR values; or tumor-infiltrative area, characterized by increased perfusion. Tumor-infiltrative area demonstrated a higher malignant pattern on MRS compared to areas of vasogenic-edema. Substantial reductions of the enhanced T-1 -weighted (58 +/- 10%) and hyperintense FLAIR (53 +/- 9%) lesion volumes were detected mainly during the first weeks of therapy, with a shift to an infiltrative pattern of tumor progression thereafter, as detected by an increase in tumor-infiltrative area in the majority of patients, which correlated with progression-free survival (week 8: r = 0.86, p = 0.003, week 16: r= 0.99, p = 0.001). Conclusion: Characterization of non-enhancing hyperintense FLAIR lesion area in GB patients can provide an MR-based biomarker, indicating a shift to an infiltrative progression pattern, and may improve therapy response assessment in patients following bevacizumab therapy. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1250 / 1256
页数:7
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