IDH-Mutation Is a Weak Predictor of Long-Term Survival in Glioblastoma Patients

被引:48
作者
Amelot, Aymeric [1 ]
De Cremoux, Patricia [2 ]
Quillien, Veronique [3 ]
Polivka, Marc [4 ]
Adle-Biassette, Homa [4 ]
Lehmann-Che, Jacqueline [2 ]
Francoise, Laurence [2 ]
Carpentier, Antoine F. [5 ]
George, Bernard [1 ,6 ]
Mandonnet, Emmanuel [1 ,6 ,7 ]
Froelich, Sebastien [1 ,6 ]
机构
[1] Lariboisiere Hosp, AP HP, Dept Neurosurg, Paris, France
[2] St Louis Hosp, AP HP, Dept Biochem, Mol Oncol Unit, Paris, France
[3] Ctr Eugene Marquis, Dept Biol, F-35042 Rennes, France
[4] Lariboisiere Hosp, AP HP, Dept Pathol, Paris, France
[5] Avicennes Hosp, AP HP, Dept Neurol, Bobigny, France
[6] Univ Paris Diderot, Sorbonne Paris Cite, Paris, France
[7] IMNC, UMR 8165, Orsay, France
来源
PLOS ONE | 2015年 / 10卷 / 07期
关键词
PROGNOSTIC VALUE; MULTIFORME; TEMOZOLOMIDE; MGMT; METHYLATION; RESECTION; IMMUNOHISTOCHEMISTRY; SERIES; EXTENT;
D O I
10.1371/journal.pone.0130596
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background A very small proportion of patients diagnosed with glioblastoma (GBM) survive more than 3 years. Isocitrate dehydrogenase 1 or 2 (IDH1/2) mutations define a small subgroup of GBM patients with favourable prognosis. However, it remains controversial whether long-term survivors (LTS) are found among those IDH1/2 mutated patients. Methods We retrospectively analyzed 207 GBM patients followed at Lariboisiere Hospital (Paris) between 2005 and 2010. Clinical parameters were obtained from medical records. Mutations of IDH1/2 were analyzed in these patients, by immunohistochemistry for the R132H mutation of IDH1 and by high-resolution melting-curve analysis, followed by Sanger sequencing for IDH1 and IDH2 exon 4 mutations. Mutation rates in LTS and non-LTS groups were compared by Chi square Pearson test. Results Seventeen patients with survival >3 years were identified (8.2% of the total series). The median overall survival in long-term survivors was 4.6 years. Subgroup analysis found that the median age at diagnosis was significantly higher for non long-term survivors (non-LTS) compared to LTS (60 versus 51 years, p <0.03). The difference in the rate of IDH mutation between non-LTS and LTS was statistically not significant (1.16% versus 5.9%, p = 0.144). Among LTS, 10 out of 16 tumors presented a methylation of MGMT promoter. Conclusions This study confirms that long-term survival in GBM patients is if at all only weakly correlated to IDH-mutation.
引用
收藏
页数:13
相关论文
共 46 条
[1]   Racial/ethnic differences in survival among elderly patients with a primary glioblastoma [J].
Barnholtz-Sloan, Jill S. ;
Maldonado, John L. ;
Williams, Vonetta L. ;
Curry, William T. ;
Rodkey, Elizabeth A. ;
Barker, Frederick G., II ;
Sloan, Andrew E. .
JOURNAL OF NEURO-ONCOLOGY, 2007, 85 (02) :171-180
[2]  
Burton EC, 2002, CLIN CANCER RES, V8, P180
[3]   IDH1 mutation is associated with improved overall survival in patients with glioblastoma: a meta-analysis [J].
Cheng, Hong-Bin ;
Yue, Wu ;
Xie, Chen ;
Zhang, Ru-You ;
Hu, Shao-Shan ;
Wang, Zhi .
TUMOR BIOLOGY, 2013, 34 (06) :3555-3559
[4]   DNA Methylation, Isocitrate Dehydrogenase Mutation, and Survival in Glioma [J].
Christensen, Brock C. ;
Smith, Ashley A. ;
Zheng, Shichun ;
Koestler, Devin C. ;
Houseman, E. Andres ;
Marsit, Carmen J. ;
Wiemels, Joseph L. ;
Nelson, Heather H. ;
Karagas, Margaret R. ;
Wrensch, Margaret R. ;
Kelsey, Karl T. ;
Wiencke, John K. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2011, 103 (02) :143-153
[5]   A clinicopathological and molecular analysis of glioblastoma multiforme with long-term survival [J].
Das, Prasenjit ;
Puri, Tarun ;
Jha, Prerana ;
Pathak, Pankaj ;
Joshi, Nikhil ;
Suri, Vaishali ;
Sharma, Mehar Chand ;
Sharma, Bhawani S. ;
Mahapatra, A. K. ;
Suri, Ashish ;
Sarkar, Chitra .
JOURNAL OF CLINICAL NEUROSCIENCE, 2011, 18 (01) :66-70
[6]   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
[7]   Transcriptional diversity of long-term glioblastoma survivors [J].
Gerber, Naamit K. ;
Goenka, Anuj ;
Turcan, Sevin ;
Reyngold, Marsha ;
Makarov, Vladimir ;
Kannan, Kasthuri ;
Beal, Kathryn ;
Omuro, Antonio ;
Yamada, Yoshiya ;
Gutin, Phillip ;
Brennan, Cameron W. ;
Huse, Jason T. ;
Chan, Timothy A. .
NEURO-ONCOLOGY, 2014, 16 (09) :1186-1195
[8]   Dose-Dense Temozolomide for Newly Diagnosed Glioblastoma: A Randomized Phase III Clinical Trial [J].
Gilbert, Mark R. ;
Wang, Meihua ;
Aldape, Kenneth D. ;
Stupp, Roger ;
Hegi, Monika E. ;
Jaeckle, Kurt A. ;
Armstrong, Terri S. ;
Wefel, Jeffrey S. ;
Won, Minhee ;
Blumenthal, Deborah T. ;
Mahajan, Anita ;
Schultz, Christopher J. ;
Erridge, Sara ;
Baumert, Brigitta ;
Hopkins, Kristen I. ;
Tzuk-Shina, Tzahala ;
Brown, Paul D. ;
Chakravarti, Arnab ;
Curran, Walter J., Jr. ;
Mehta, Minesh P. .
JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (32) :4085-+
[9]   Long-Term Survival in Primary Glioblastoma With Versus Without Isocitrate Dehydrogenase Mutations [J].
Hartmann, Christian ;
Hentschel, Bettina ;
Simon, Matthias ;
Westphal, Manfred ;
Schackert, Gabriele ;
Tonn, Joerg C. ;
Loeffler, Markus ;
Reifenberger, Guido ;
Pietsch, Torsten ;
von Deimling, Andreas ;
Weller, Michael .
CLINICAL CANCER RESEARCH, 2013, 19 (18) :5146-5157
[10]   MGMT gene silencing and benefit from temozolomide in glioblastoma [J].
Hegi, ME ;
Diserens, A ;
Gorlia, T ;
Hamou, M ;
de Tribolet, N ;
Weller, M ;
Kros, JM ;
Hainfellner, JA ;
Mason, W ;
Mariani, L ;
Bromberg, JEC ;
Hau, P ;
Mirimanoff, RO ;
Cairncross, JG ;
Janzer, RC ;
Stupp, R .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (10) :997-1003