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@ARTICLE{Witt:142207,
author = {H. Witt$^*$ and D. Gramatzki and B. Hentschel and K.
Pajtler$^*$ and J. Felsberg$^*$ and G. Schackert and M.
Löffler and D. Capper$^*$ and F. Sahm$^*$ and M. Sill$^*$
and A. von Deimling$^*$ and M. Kool$^*$ and U. Herrlinger
and M. Westphal and T. Pietsch and G. Reifenberger$^*$ and
S. Pfister$^*$ and J. C. Tonn and M. Weller},
collaboration = {G. G. Network},
title = {{DNA} methylation-based classification of ependymomas in
adulthood: implications for diagnosis and treatment.},
journal = {Neuro-Oncology},
volume = {20},
number = {12},
issn = {1523-5866},
address = {Oxford},
publisher = {Oxford Univ. Press},
reportid = {DKFZ-2019-00021},
pages = {1616 - 1624},
year = {2018},
abstract = {Ependymal tumors are glial tumors that commonly manifest in
children and young adults. Their classification has remained
entirely morphological until recently, and surgery and
radiotherapy are the main treatment options, especially in
adults. Here we sought to correlate DNA methylation profiles
with clinical and pathological characteristics in the
prospective cohort of the German Glioma Network.Tumors from
122 adult patients with myxopapillary ependymoma,
ependymoma, anaplastic ependymoma, subependymoma, or RELA
fusion-positive ependymoma classified according to the World
Health Organization (WHO) 2016 were subjected to DNA
methylation profiling using the Illumina HumanMethylation450
BeadChip platform. Molecular data were correlated with
histologic features and clinical characteristics.At a median
follow-up of 86.7 months, only 22 patients experienced
progression $(18.0\%)$ and 13 patients $(10.7\%)$ died. Each
tumor could be assigned to one of the previously defined
molecular ependymoma subgroups. All histologic
subependymomas corresponded to subependymoma (SE) DNA
methylation subgroups, but the reverse was not true: 19
histologic ependymomas (WHO grade II) were allocated to
molecular SE groups. Similarly, all histological
myxopapillary ependymomas were assigned to the molecularly
defined spinal myxopapillary ependymoma (SP-MPE) class, but
this molecular subgroup additionally included 15 WHO grade
II ependymomas by histology. Overall, WHO grade II
ependymomas distributed into 7 molecular subgroups.Most
adult patients with ependymoma show a favorable prognosis.
Molecular classification may provide diagnostic and
prognostic information beyond histology and facilitate
patient stratification in future clinical trials. The
prognostic significance of a subependymoma or myxopapillary
ependymoma DNA methylation phenotype without corresponding
histology requires further study.1. Ependymoma diagnosed in
adult patients most often shows a good prognosis. 2.
Molecular classification can support diagnostic and
prognostic information beyond histology.},
cin = {B062 / G380 / L101 / L401 / L201 / L301 / L701},
ddc = {610},
cid = {I:(DE-He78)B062-20160331 / I:(DE-He78)G380-20160331 /
I:(DE-He78)L101-20160331 / I:(DE-He78)L401-20160331 /
I:(DE-He78)L201-20160331 / I:(DE-He78)L301-20160331 /
I:(DE-He78)L701-20160331},
pnm = {312 - Functional and structural genomics (POF3-312)},
pid = {G:(DE-HGF)POF3-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:30053291},
pmc = {pmc:PMC6231197},
doi = {10.1093/neuonc/noy118},
url = {https://inrepo02.dkfz.de/record/142207},
}