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Published in: Acta Neuropathologica 6/2017

01-12-2017 | Correspondence

Molecular and clinical heterogeneity of adult diffuse low-grade IDH wild-type gliomas: assessment of TERT promoter mutation and chromosome 7 and 10 copy number status allows superior prognostic stratification

Authors: Maarten M. J. Wijnenga, Hendrikus J. Dubbink, Pim J. French, Nathalie E. Synhaeve, Winand N. M. Dinjens, Peggy N. Atmodimedjo, Johan M. Kros, Clemens M. F. Dirven, Arnaud J. P. E. Vincent, Martin J. van den Bent

Published in: Acta Neuropathologica | Issue 6/2017

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Excerpt

With the 2016 revision of the World Health Organization classification of tumors of the central nervous system (WHO 2016) testing for the presence of mutations in isocitrate dehydrogenase 1 and 2 (IDH) and chromosome 1p/19q status is the cornerstone of glioma classification [5]. Approximately 80% of diffuse low-grade (grades II and III) gliomas (DLGG) are IDH mutated and have a relatively favorable prognosis compared to their IDH wild-type (IDHwt) counterparts [2]. The prognosis of IDHwt DLGG is almost similar to primary glioblastoma and genetic aberrations that are seen in primary glioblastoma are also reported in IDHwt DLGG: the combination of trisomy of whole chromosome 7 and loss of chromosomal arm 10q (+ 7/− 10q), and telomerase reverse transcriptase gene promoter (TERTp) mutations [2, 6, 7]. However, + 7/− 10q or TERTp mutations are not part of the WHO 2016 criteria and not all IDHwt DLGG have these specific molecular aberrations [2, 5]. Although clinical trials have not been performed, in view of their poor prognosis, aggressive treatment regimens for IDHwt DLGG have been suggested. However, as this is not a well-defined separate entity, the question remains whether IDHwt DLGG classified according to current WHO classification qualifies as a single entity, with sufficient information to estimate prognosis adequately, and therefore, guide treatment, or if the assessment of additional markers is necessary and if so which. A recent study by Aibaidula et al. showed that IDHwt DLGG are prognostically heterogeneous and that markers like TERTp, EGFR amplification and H3F3A mutation could be of additional value [1]. The prognostic role of + 7/− 10q and its relationship with TERTp mutations were not reported, however. In this study, we report on the impact of additional molecular markers, including + 7/− 10q and TERTp, on overall survival in adult IDHwt DLGG. …
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Literature
1.
2.
go back to reference Cancer Genome Atlas Research N, Brat DJ, Verhaak RG, Aldape KD, Yung WK, Salama SR, Cooper LA, Rheinbay E, Miller CR, Vitucci M et al (2015) Comprehensive, integrative genomic analysis of diffuse lower-grade gliomas. N Engl J Med 372:2481–2498. doi:10.1056/NEJMoa1402121 CrossRef Cancer Genome Atlas Research N, Brat DJ, Verhaak RG, Aldape KD, Yung WK, Salama SR, Cooper LA, Rheinbay E, Miller CR, Vitucci M et al (2015) Comprehensive, integrative genomic analysis of diffuse lower-grade gliomas. N Engl J Med 372:2481–2498. doi:10.​1056/​NEJMoa1402121 CrossRef
3.
go back to reference Dubbink HJ, Atmodimedjo PN, Kros JM, French PJ, Sanson M, Idbaih A, Wesseling P, Enting R, Spliet W, Tijssen C et al (2016) Molecular classification of anaplastic oligodendroglioma using next-generation sequencing: a report of the prospective randomized EORTC Brain Tumor Group 26951 phase III trial. Neuro Oncol 18:388–400. doi:10.1093/neuonc/nov182 CrossRefPubMed Dubbink HJ, Atmodimedjo PN, Kros JM, French PJ, Sanson M, Idbaih A, Wesseling P, Enting R, Spliet W, Tijssen C et al (2016) Molecular classification of anaplastic oligodendroglioma using next-generation sequencing: a report of the prospective randomized EORTC Brain Tumor Group 26951 phase III trial. Neuro Oncol 18:388–400. doi:10.​1093/​neuonc/​nov182 CrossRefPubMed
4.
go back to reference Dubbink HJ, Atmodimedjo PN, van Marion R, Krol NM, Riegman PH, Kros JM, van den Bent MJ, Dinjens WN (2016) Diagnostic detection of allelic losses and imbalances by next-generation sequencing: 1p/19q co-deletion analysis of gliomas. J Mol Diagn 18:775–786. doi:10.1016/j.jmoldx.2016.06.002 CrossRefPubMed Dubbink HJ, Atmodimedjo PN, van Marion R, Krol NM, Riegman PH, Kros JM, van den Bent MJ, Dinjens WN (2016) Diagnostic detection of allelic losses and imbalances by next-generation sequencing: 1p/19q co-deletion analysis of gliomas. J Mol Diagn 18:775–786. doi:10.​1016/​j.​jmoldx.​2016.​06.​002 CrossRefPubMed
5.
go back to reference Louis DN, Perry A, Reifenberger G, von Deimling A, Figarella-Branger D, Cavenee WK, Ohgaki H, Wiestler OD, Kleihues P, Ellison DW (2016) The 2016 World Health Organization classification of tumors of the central nervous system: a summary. Acta Neuropathol 131:803–820. doi:10.1007/s00401-016-1545-1 CrossRefPubMed Louis DN, Perry A, Reifenberger G, von Deimling A, Figarella-Branger D, Cavenee WK, Ohgaki H, Wiestler OD, Kleihues P, Ellison DW (2016) The 2016 World Health Organization classification of tumors of the central nervous system: a summary. Acta Neuropathol 131:803–820. doi:10.​1007/​s00401-016-1545-1 CrossRefPubMed
7.
go back to reference Weller M, Weber RG, Willscher E, Riehmer V, Hentschel B, Kreuz M, Felsberg J, Beyer U, Loffler-Wirth H, Kaulich K et al (2015) Molecular classification of diffuse cerebral WHO grade II/III gliomas using genome- and transcriptome-wide profiling improves stratification of prognostically distinct patient groups. Acta Neuropathol 129:679–693. doi:10.1007/s00401-015-1409-0 CrossRefPubMed Weller M, Weber RG, Willscher E, Riehmer V, Hentschel B, Kreuz M, Felsberg J, Beyer U, Loffler-Wirth H, Kaulich K et al (2015) Molecular classification of diffuse cerebral WHO grade II/III gliomas using genome- and transcriptome-wide profiling improves stratification of prognostically distinct patient groups. Acta Neuropathol 129:679–693. doi:10.​1007/​s00401-015-1409-0 CrossRefPubMed
8.
go back to reference Wijnenga MMJ, French PJ, Dubbink HD, Dinjens WNM, Atmodimedjo PN, Kros JM, Smits M, Gahrmann R, Rutten GJ, Verheul JB et al (2017) The impact of surgery in molecularly defined low-grade glioma: an integrated clinical, radiological and molecular analysis. Neuro Oncol. doi:10.1093/neuonc/nox176 PubMed Wijnenga MMJ, French PJ, Dubbink HD, Dinjens WNM, Atmodimedjo PN, Kros JM, Smits M, Gahrmann R, Rutten GJ, Verheul JB et al (2017) The impact of surgery in molecularly defined low-grade glioma: an integrated clinical, radiological and molecular analysis. Neuro Oncol. doi:10.​1093/​neuonc/​nox176 PubMed
Metadata
Title
Molecular and clinical heterogeneity of adult diffuse low-grade IDH wild-type gliomas: assessment of TERT promoter mutation and chromosome 7 and 10 copy number status allows superior prognostic stratification
Authors
Maarten M. J. Wijnenga
Hendrikus J. Dubbink
Pim J. French
Nathalie E. Synhaeve
Winand N. M. Dinjens
Peggy N. Atmodimedjo
Johan M. Kros
Clemens M. F. Dirven
Arnaud J. P. E. Vincent
Martin J. van den Bent
Publication date
01-12-2017
Publisher
Springer Berlin Heidelberg
Published in
Acta Neuropathologica / Issue 6/2017
Print ISSN: 0001-6322
Electronic ISSN: 1432-0533
DOI
https://doi.org/10.1007/s00401-017-1781-z

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