Correlation of MRI sequences to assess progressive glioblastoma multiforme treated with bevacizumab

被引:9
作者
Thompson, Eric M. [1 ]
Dosa, Edit [2 ]
Kraemer, Dale F. [3 ,4 ,5 ]
Neuwelt, Edward A. [1 ,2 ,6 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Neurol Surg, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Dept Neurol, Portland, OR 97239 USA
[3] Oregon Hlth & Sci Univ, Dept Publ Hlth & Prevent Med, Portland, OR 97239 USA
[4] Oregon Hlth & Sci Univ, Dept Med Informat & Clin Epidemiol, Portland, OR 97239 USA
[5] Oregon Hlth & Sci Univ, Dept Pharm Practice, Oregon State Univ, Coll Pharm, Portland, OR 97239 USA
[6] Portland VA Med Ctr, Portland, OR 97239 USA
关键词
Bevacizumab; Macdonald criteria; FLAIR; Progressive malignant glioma; PHASE-II; IRINOTECAN; EFFICACY; GLIOMAS; CARBOPLATIN; SURVIVAL; CRITERIA; VOLUME; TUMORS;
D O I
10.1007/s11060-010-0397-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the context of bevacizumab therapy for the treatment of progressive malignant gliomas, it is currently unclear how different magnetic resonance imaging (MRI) sequences correlate with each other over time. The objective of this study was to determine if a reliable and predictable relationship over time exists between post-gadolinium based contrast agent T1-weighted (T1 + GBCA), T2-weighted, and FLAIR MRI in patients with progressive glioblastoma multiforme (GBM) receiving bevacizumab and chemotherapy. The MRI lesion volumes of 10 patients with progressive GBM that received bevacizumab plus chemotherapy were manually calculated by two independent reviewers. T2 and FLAIR volumes were analyzed by analysis of covariance (ANCOVA) as a function of T1 + GBCA lesion enhancement volume, reviewer, and time interval between MRI acquisitions. Pearson product moment correlation (r) was used to compare pre and post treatment volumes for the group of 10 patients and for each individual patient over their treatment course. ANCOVA demonstrated a significant association between T1 + GBCA and T2-weighted volumes (P = 0.0006) and between T1 + GBCA and FLAIR volumes (P < 0.0001). These associations remained constant over time. The correlation between T1 + GBCA and both T2-weighted and FLAIR volumes improved after bevacizumab treatment. Individual correlations between T1 + GBCA and FLAIR were strong (r a parts per thousand yen 0.63) with one exception, while correlations between T1 + GBCA and T2 were more variable (r = 0.18-0.99). These findings suggest that FLAIR MRI should be evaluated in addition to T1 + GBCA MRI when evaluating GBM responses.
引用
收藏
页码:353 / 360
页数:8
相关论文
共 22 条
[1]   Time course of imaging changes of GBM during extended bevacizumab treatment [J].
Ananthnarayan, Suchitra ;
Bahng, Jennie ;
Roring, James ;
Nghiemphu, Phioanh ;
Lai, Albert ;
Cloughesy, Timothy ;
Pope, Whitney B. .
JOURNAL OF NEURO-ONCOLOGY, 2008, 88 (03) :339-347
[2]   AZD2171, a pan-VEGF receptor tyrosine kinase inhibitor, normalizes tumor vasculature and alleviates edema in glioblastoma patients [J].
Batchelor, Tracy T. ;
Sorensen, A. Gregory ;
di Tomaso, Emmanuelle ;
Zhang, Wei-Ting ;
Duda, Dan G. ;
Cohen, Kenneth S. ;
Kozak, Kevin R. ;
Cahill, Daniel P. ;
Chen, Poe-Jou ;
Zhu, Mingwang ;
Ancukiewicz, Marek ;
Mrugala, Maciej M. ;
Plotkin, Scott ;
Drappatz, Jan ;
Louis, David N. ;
Ivy, Percy ;
Scadden, David T. ;
Benner, Thomas ;
Loeffler, Jay S. ;
Wen, Patrick Y. ;
Jain, Rakesh K. .
CANCER CELL, 2007, 11 (01) :83-95
[3]   Treatment with bevacizumab and irinotecan for recurrent high-grade glial tumors [J].
Bokstein, Felix ;
Shpigel, Shulim ;
Blumenthal, Deborah T. .
CANCER, 2008, 112 (10) :2267-2273
[4]   POTENTIAL FOR DIFFERENTIATION OF PSEUDOPROGRESSION FROM TRUE TUMOR PROGRESSION WITH DYNAMIC SUSCEPTIBILITY-WEIGHTED CONTRAST-ENHANCED MAGNETIC RESONANCE IMAGING USING FERUMOXYTOL VS. GADOTERIDOL: A PILOT STUDY [J].
Gahramanov, Seymur ;
Raslan, Ahmed M. ;
Muldoon, Leslie L. ;
Hamilton, Bronwyn E. ;
Rooney, William D. ;
Varallyay, Csanad G. ;
Njus, Jeffrey M. ;
Haluska, Marianne ;
Neuwelt, Edward A. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2011, 79 (02) :514-523
[5]  
IWAMA T, 1991, Neurological Research, V13, P48
[6]   Efficacy and MRI of rituximab and methotrexate treatment in a nude rat model of CNS lymphoma [J].
Jahnke, Kristoph ;
Muldoon, Leslie L. ;
Varallyay, Csanad G. ;
Lewin, Seth J. ;
Brown, Robert D. ;
Kraemer, Dale F. ;
Soussain, Carole ;
Neuwelt, Edward A. .
NEURO-ONCOLOGY, 2009, 11 (05) :503-513
[7]   Bevacizumab and carboplatin increase survival and asymptomatic tumor volume in a glioma model [J].
Jahnke, Kristoph ;
Muldoon, Leslie L. ;
Varallyay, Csanad G. ;
Lewin, Seth J. ;
Kraemer, Dale F. ;
Neuwelt, Edward A. .
NEURO-ONCOLOGY, 2009, 11 (02) :142-150
[8]   Irinotecan and bevacizumab in progressive primary brain tumors, an evaluation of efficacy and safety [J].
Kang, Tyler Y. ;
Jin, Tony ;
Elinzano, Heinrich ;
Peereboom, David .
JOURNAL OF NEURO-ONCOLOGY, 2008, 89 (01) :113-118
[9]   RANDOMIZED DOUBLE-BLIND PLACEBO-CONTROLLED TRIAL OF BEVACIZUMAB THERAPY FOR RADIATION NECROSIS OF THE CENTRAL NERVOUS SYSTEM [J].
Levin, Victor A. ;
Bidaut, Luc ;
Hou, Ping ;
Kumar, Ashok J. ;
Wefel, Jeffrey S. ;
Bekele, B. Nebiyou ;
Prabhu, Sujit ;
Loghin, Monica ;
Gilbert, Mark R. ;
Jackson, Edward F. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2011, 79 (05) :1487-1495
[10]   RESPONSE CRITERIA FOR PHASE-II STUDIES OF SUPRATENTORIAL MALIGNANT GLIOMA [J].
MACDONALD, DR ;
CASCINO, TL ;
SCHOLD, SC ;
CAIRNCROSS, JG .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (07) :1277-1280