Patterns of Tumor Contrast Enhancement Predict the Prognosis of Anaplastic Gliomas with IDH1 Mutation

被引:43
作者
Wang, Y. Y. [1 ,3 ]
Wang, K. [2 ]
Li, S. W. [2 ]
Wang, J. F. [1 ]
Ma, J. [2 ]
Jiang, T. [1 ,3 ,4 ]
Dai, J. P. [2 ,3 ]
机构
[1] Beijing Tian Tan Hosp, Dept Neurosurg, Beijing, Peoples R China
[2] Beijing Tian Tan Hosp, Dept Neuroradiol, Beijing, Peoples R China
[3] Capital Med Univ, Beijing Neurosurg Inst, Beijing 100050, Peoples R China
[4] Beijing Inst Brain Disorders, Ctr Brain Tumor, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
CODON; 132; MUTATION; SURVIVAL; ASTROCYTOMAS; CLASSIFICATION; AGE;
D O I
10.3174/ajnr.A4407
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BACKGROUND AND PURPOSE: It is proposed that isocitrate dehydrogenase 1 (IDH1) mutation predicts the outcome in patients with high-grade glioma. In addition, contrast enhancement on preoperative MR imaging reflects tumor biologic features. Patients with anaplastic glioma with the IDH1 mutation were evaluated by using MR imaging to determine whether tumor enhancement is a prognostic factor and can be used to predict survival. MATERIALS AND METHODS: A cohort of 216 patients with histologically confirmed anaplastic glioma was reviewed retrospectively. Tumor contrast-enhancement patterns were classified on the basis of preoperative Tl contrast MR images. Tumor IDH1 status was examined by using RNA sequencing. We used univariate analysis and the multivariate Cox model to evaluate the prognostic value of the IDH1 mutation and tumor contrast-enhancement pattern for progression-free survival and overall survival. RESULTS: In all 216 patients, IDH1mutation was associated with longer progression-free survival (P =.004, hazard ratio =0.439) and overall survival (P=.002, hazard ratio = 0.406). For patients with IDH1 mutant anaplastic glioma, the absence of contrast enhancement was associated with longer progression-free survival (P =.038, hazard ratio = 0.473) and overall survival (P =.043, hazard ratio = 0.436). Furthermore, we were able to stratify the progression-free survival and overall survival of patients with IDH1 mutation by using the tumor contrast-enhancement patterns (P =.022 and 0.029, respectively; log-rank). CONCLUSIONS: Tumor enhancement on postcontrast MR imaging is a valuable prognostic factor for patients with anaplastic glioma and IDH1 mutation. Furthermore, the contrast-enhancement patterns could potentially be used to stratify the survival outcome of such patients.
引用
收藏
页码:2023 / 2029
页数:7
相关论文
共 27 条
[1]   Analysis of the IDH1 codon 132 mutation in brain tumors [J].
Balss, Joerg ;
Meyer, Jochen ;
Mueller, Wolf ;
Korshunov, Andrey ;
Hartmann, Christian ;
von Deimling, Andreas .
ACTA NEUROPATHOLOGICA, 2008, 116 (06) :597-602
[2]   IDH1 mutant malignant astrocytomas are more amenable to surgical resection and have a survival benefit associated with maximal surgical resection [J].
Beiko, Jason ;
Suki, Dima ;
Hess, Kenneth R. ;
Fox, Benjamin D. ;
Cheung, Vincent ;
Cabral, Matthew ;
Shonka, Nicole ;
Gilbert, Mark R. ;
Sawaya, Raymond ;
Prabhu, Sujit S. ;
Weinberg, Jeffrey ;
Lang, Frederick F. ;
Aldape, Kenneth D. ;
Sulman, Erik P. ;
Rao, Ganesh ;
McCutcheon, Ian E. ;
Cahill, Daniel P. .
NEURO-ONCOLOGY, 2014, 16 (01) :81-91
[3]   Relationship between Tumor Enhancement, Edema, IDH1 Mutational Status, MGMT Promoter Methylation, and Survival in Glioblastoma [J].
Carrillo, J. A. ;
Lai, A. ;
Nghiemphu, P. L. ;
Kim, H. J. ;
Phillips, H. S. ;
Kharbanda, S. ;
Moftakhar, P. ;
Lalaezari, S. ;
Yong, W. ;
Ellingson, B. M. ;
Cloughesy, T. F. ;
Pope, W. B. .
AMERICAN JOURNAL OF NEURORADIOLOGY, 2012, 33 (07) :1349-1355
[4]   Prognostic significance of contrast-enhancing anaplastic astrocytomas in adults Clinical article [J].
Chaichana, Kaisorn L. ;
Kosztowski, Thomas ;
Niranjan, Ashwini ;
Olivi, Alessandro ;
Weingart, Jon D. ;
Laterra, John ;
Brem, Henry ;
Quinones-Hinojosa, Alfredo .
JOURNAL OF NEUROSURGERY, 2010, 113 (02) :286-292
[5]   Anaplastic Gliomas [J].
DeAngelis, Lisa M. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (35) :5861-5862
[6]   From genomics to the clinic: biological and translational insights of mutant IDH1/2 in glioma [J].
Dunn, Gavin P. ;
Andronesi, Ovidiu C. ;
Cahill, Daniel P. .
NEUROSURGICAL FOCUS, 2013, 34 (02)
[7]   Combining two biomarkers, IDH1/2 mutations and 1p/19q codeletion, to stratify anaplastic oligodendroglioma in three groups: a single-center experience [J].
Frenel, J. S. ;
Leux, C. ;
Loussouarn, D. ;
Le Loupp, A. -G. ;
Leclair, F. ;
Aumont, M. ;
Mervoyer, A. ;
Martin, S. ;
Denis, M. G. ;
Campone, M. .
JOURNAL OF NEURO-ONCOLOGY, 2013, 114 (01) :85-91
[8]   Patients with IDH1 wild type anaplastic astrocytomas exhibit worse prognosis than IDH1-mutated glioblastomas, and IDH1 mutation status accounts for the unfavorable prognostic effect of higher age: implications for classification of gliomas [J].
Hartmann, Christian ;
Hentschel, Bettina ;
Wick, Wolfgang ;
Capper, David ;
Felsberg, Joerg ;
Simon, Matthias ;
Westphal, Manfred ;
Schackert, Gabriele ;
Meyermann, Richard ;
Pietsch, Torsten ;
Reifenberger, Guido ;
Weller, Michael ;
Loeffler, Markus ;
von Deimling, Andreas .
ACTA NEUROPATHOLOGICA, 2010, 120 (06) :707-718
[9]   Type and frequency of IDH1 and IDH2 mutations are related to astrocytic and oligodendroglial differentiation and age: a study of 1,010 diffuse gliomas [J].
Hartmann, Christian ;
Meyer, Jochen ;
Balss, Joerg ;
Capper, David ;
Mueller, Wolf ;
Christians, Arne ;
Felsberg, Joerg ;
Wolter, Marietta ;
Mawrin, Christian ;
Wick, Wolfgang ;
Weller, Michael ;
Herold-Mende, Christel ;
Unterberg, Andreas ;
Jeuken, Judith W. M. ;
Wesseling, Peter ;
Reifenberger, Guido ;
von Deimling, Andreas .
ACTA NEUROPATHOLOGICA, 2009, 118 (04) :469-474
[10]   Frequent ATRX, CIC, FUBP1 and IDH1 mutations refine the classification of malignant gliomas [J].
Jiao, Yuchen ;
Killela, Patrick J. ;
Reitman, Zachary J. ;
Rasheed, B. Ahmed ;
Heaphy, Christopher M. ;
de Wilde, Roeland F. ;
Rodriguez, Fausto J. ;
Rosemberg, Sergio ;
Oba-Shinjo, Sueli Mieko ;
Marie, Suely Kazue Nagahashi ;
Bettegowda, Chetan ;
Agrawal, Nishant ;
Lipp, Eric ;
Pirozzi, Christopher J. ;
Lopez, Giselle Y. ;
He, Yiping ;
Friedman, Henry S. ;
Friedman, Allan H. ;
Riggins, Gregory J. ;
Holdhoff, Matthias ;
Burger, Peter ;
McLendon, Roger E. ;
Bigner, Darell D. ;
Vogelstein, Bert ;
Meeker, Alan K. ;
Kinzler, Kenneth W. ;
Papadopoulos, Nickolas ;
Diaz, Luis A., Jr. ;
Yan, Hai .
ONCOTARGET, 2012, 3 (07) :709-722