Quantification of edema reduction using differential quantitative T2 (DQT2) relaxometry mapping in recurrent glioblastoma treated with bevacizumab

被引:53
作者
Ellingson, Benjamin M. [1 ,2 ]
Cloughesy, Timothy F. [3 ]
Lai, Albert [3 ]
Nghiemphu, Phioanh L. [3 ]
Lalezari, Shadi [3 ]
Zaw, Taryar [1 ]
Motevalibashinaeini, Kourosh [1 ]
Mischel, Paul S. [4 ]
Pope, Whitney B. [1 ]
机构
[1] Univ Calif Los Angeles, Dept Radiol Sci, David Geffen Sch Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Biomed Phys, David Geffen Sch Med, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Neurol, David Geffen Sch Med, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Dept Pathol & Lab Med, David Geffen Sch Med, Los Angeles, CA 90095 USA
关键词
GBM; Glioblastoma; Angiogenesis; DQT2; Magnetic resonance imaging; MRI; Bevacizumab; HIGH-GRADE GLIOMAS; FUNCTIONAL DIFFUSION MAPS; MAGNETIC-RESONANCE; IMAGING BIOMARKER; MALIGNANT GLIOMAS; GLIAL NEOPLASMS; BRAIN-TUMORS; PHASE-II; IRINOTECAN; MR;
D O I
10.1007/s11060-011-0638-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of the current study was to quantify the reduction in T2 signal abnormality accompanying administration of the anti-angiogenic drug bevacizumab in recurrent glioblastoma (GBM) patients using a voxel-wise differential quantitative T2 (DQT2) mapping technique. Twenty-six patients with recurrent GBM treated with bevacizumab were scanned before and 4-6 weeks after treatment on a 1.5T clinical MR scanner. Quantitative T2 maps were created from proton density and T2-weighted images acquired using a standard multi-echo fast-spin echo sequence. T2 maps after treatment were co-registered with T2 maps prior to treatment in the same patient, and then voxel-wise subtraction was performed to create DQT2 maps for each patient. Results suggest DQT2 maps allow visualization and quantification of voxel-wise T2 changes resulting from anti-VEGF therapy. Results demonstrated a significant decrease in T2 within pre-treatment T2 abnormal regions (mean reduction = 49.4 ms at 1.5T) following anti-VEGF treatment (Wilcoxon signed rank test, P < 0.0001). An elevated residual, post-treatment, median T2 was predictive of both progression-free (Log-rank, P = 0.0074) and overall survival (Log-rank, P = 0.0393).
引用
收藏
页码:111 / 119
页数:9
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