Response Assessment in Neuro-Oncology criteria, contrast enhancement and perfusion MRI for assessing progression in glioblastoma

被引:18
作者
Tensaouti, Fatima [1 ]
Khalifa, Jonathan [2 ]
Lusque, Amelie [3 ]
Plas, Benjamin [4 ]
Lotterie, Jean Albert [1 ,5 ]
Berry, Isabelle [1 ,5 ]
Laprie, Anne [1 ,2 ]
Moyal, Elizabeth Cohen-Jonathan [2 ,6 ]
Lubrano, Vincent [1 ,4 ]
机构
[1] Univ Toulouse, Toulouse NeuroImaging Ctr, ToNIC, Inserm,UPS, Toulouse, France
[2] Toulouse Univ, Dept Radiat Oncol, Claudius Regaud Inst, Canc Inst Oncopole, Toulouse, France
[3] Toulouse Univ, Dept Biostat, Claudius Regaud Inst, Canc Inst Oncopole, Toulouse, France
[4] CHU Toulouse, Dept Neurosurg, Toulouse, France
[5] CHU Toulouse, Dept Nucl Med, Toulouse, France
[6] INSERM, Toulouse Ctr Canc Res U1037, Toulouse, France
关键词
Glioblastoma; Criteria; Contrast enhancement; Perfusion magnetic resonance imaging; Disease progression; HIGH-GRADE GLIOMAS; RECURRENT GLIOBLASTOMA; ADJUVANT TEMOZOLOMIDE; MALIGNANT GLIOMA; CLINICAL-TRIAL; WORKING GROUP; PSEUDOPROGRESSION; CONCOMITANT; SURVIVAL; RANO;
D O I
10.1007/s00234-017-1899-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The purpose of the study was to evaluate Response Assessment in Neuro-Oncology (RANO) criteria in glioblastoma multiforme (GBM), with respect to the Macdonald criteria and changes in contrast-enhancement (CE) volume. Related variations in relative cerebral blood volume (rCBV) were investigated. Forty-three patients diagnosed between 2006 and 2010 were included. All underwent surgical resection, followed by temozolomide-based chemoradiation. MR images were retrospectively reviewed. Times to progression (TTPs) according to RANO criteria, Macdonald criteria and increased CE volume (CE-3D) were compared, and the percentage change in the 75th percentile of rCBV (rCBV75) was evaluated. After a median follow-up of 22.7 months, a total of 39 patients had progressed according to RANO criteria, 32 according to CE-3D, and 42 according to Macdonald. Median TTPs were 6.4, 9.3, and 6.6 months, respectively. Overall agreement was 79.07% between RANO and CE-3D and 93.02% between RANO and Macdonald. The mean percentage change in rCBV75 at RANO progression onset was over 73% in 87.5% of patients. In conclusion, our findings suggest that CE-3D criterion is not yet suitable to assess progression in routine clinical practice. Indeed, the accurate threshold is still not well defined. To date, in our opinion, early detection of disease progression by RANO combined with advanced MRI imaging techniques like MRI perfusion and diffusion remains the best way to assess disease progression. Further investigations that would examine the impact of treatment modifications after progression determined by different criteria on overall survival would be of great value.
引用
收藏
页码:1013 / 1020
页数:8
相关论文
共 33 条
[1]  
[Anonymous], 2008, P ESMRMB C VAL SPAIN
[2]   MGMT promoter methylation status can predict the incidence and outcome of pseudoprogression after concomitant radiochemotherapy in newly diagnosed glioblastoma patients [J].
Brandes, Alba A. ;
Franceschi, Enrico ;
Tosoni, Alicia ;
Blatt, Valeria ;
Pession, Annalisa ;
Tallini, Giovanni ;
Bertorelle, Roberta ;
Bartolini, Stefania ;
Calbucci, Fabio ;
Andreoli, Alvaro ;
Frezza, Giampiero ;
Leonardi, Marco ;
Spagnolli, Federica ;
Ermani, Mario .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (13) :2192-2197
[3]   Clinical investigation survival prediction in high-grade gliomas by MRI perfusion before and during early stage of RT. (vol 64, pg 876, 2006) [J].
Cao, Y ;
Tsien, CI ;
Nagesh, V ;
Junck, L ;
Ten Haken, R ;
Ross, BD ;
Chenevert, TL ;
Lawrence, TS .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2006, 65 (03) :960-960
[4]   Response Assessment Criteria for Glioblastoma: Practical Adaptation and Implementation in Clinical Trials of Antiangiogenic Therapy [J].
Chinot, Olivier L. ;
Macdonald, David R. ;
Abrey, Lauren E. ;
Zahlmann, Gudrun ;
Kerloeguen, Yannick ;
Cloughesy, Timothy F. .
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS, 2013, 13 (05)
[5]   Pseudoprogression and pseudoresponse: Challenges in brain tumor imaging [J].
Clarke, Jennifer L. ;
Chang, Susan .
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS, 2009, 9 (03) :241-246
[6]   Transient postictal MRI changes in patients with brain tumors may mimic disease progression [J].
Finn, Michael A. ;
Blumenthal, Deborah T. ;
Salzman, Karen L. ;
Jensen, Randy L. .
SURGICAL NEUROLOGY, 2007, 67 (03) :246-250
[7]   Comparison of 2D (RANO) and volumetric methods for assessment of recurrent glioblastoma treated with bevacizumab-a report from the BELOB trial [J].
Gahrmann, Renske ;
van den Bent, Martin ;
van der Holt, Bronno ;
Vernhout, Rene Michel ;
Taal, Walter ;
Vos, Maaike ;
de Groot, Jan Cees ;
Beerepoot, Laurens Victor ;
Buter, Jan ;
Flach, Zwenneke Hendrieke ;
Hanse, Monique ;
Jasperse, Bas ;
Smits, Marion .
NEURO-ONCOLOGY, 2017, 19 (06) :853-861
[8]   Brain tumor imaging in clinical trials [J].
Henson, J. W. ;
Ulmer, S. ;
Harris, G. J. .
AMERICAN JOURNAL OF NEURORADIOLOGY, 2008, 29 (03) :419-424
[9]   Relative Cerebral Blood Volume Values to Differentiate High-Grade Glioma Recurrence from Posttreatment Radiation Effect: Direct Correlation between Image-Guided Tissue Histopathology and Localized Dynamic Susceptibility-Weighted Contrast-Enhanced Perfusion MR Imaging Measurements [J].
Hu, L. S. ;
Baxter, L. C. ;
Smith, K. A. ;
Feuerstein, B. G. ;
Karis, J. P. ;
Eschlbacher, J. M. ;
Coons, S. W. ;
Nakaji, P. ;
Yeh, R. F. ;
Debbins, J. ;
Heiserman, J. E. .
AMERICAN JOURNAL OF NEURORADIOLOGY, 2009, 30 (03) :552-558
[10]   Reevaluating the imaging definition of tumor progression: perfusion MRI quantifies recurrent glioblastoma tumor fraction, pseudoprogression, and radiation necrosis to predict survival [J].
Hu, Leland S. ;
Eschbacher, Jennifer M. ;
Heiserman, Joseph E. ;
Dueck, Amylou C. ;
Shapiro, William R. ;
Liu, Seban ;
Karis, John P. ;
Smith, Kris A. ;
Coons, Stephen W. ;
Nakaji, Peter ;
Spetzler, Robert F. ;
Feuerstein, Burt G. ;
Debbins, Josef ;
Baxter, Leslie C. .
NEURO-ONCOLOGY, 2012, 14 (07) :919-930