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@ARTICLE{CiobanuCaraus:284754,
author = {O. Ciobanu-Caraus and T. Czech and A. Peyrl and C. Haberler
and G. Kasprian and J. Furtner and M. Kool$^*$ and M.
Sill$^*$ and J. M. Frischer and A. Cho and I. Slavc and K.
Rössler and J. Gojo and C. Dorfer},
title = {{T}he {S}ite of {O}rigin of {M}edulloblastoma: {S}urgical
{O}bservations {C}orrelated to {M}olecular {G}roups.},
journal = {Cancers},
volume = {15},
number = {19},
issn = {2072-6694},
address = {Basel},
publisher = {MDPI},
reportid = {DKFZ-2023-02065},
pages = {4877},
year = {2023},
abstract = {Developmental gene expression data from medulloblastoma
(MB) suggest that WNT-MB originates from the region of the
embryonic lower rhombic lip (LRL), whereas SHH-MB and
non-WNT/non-SHH MB arise from cerebellar precursor matrix
regions. This study aimed to analyze detailed intraoperative
data with regard to the site of origin (STO) and compare
these findings with the hypothesized regions of origin
associated with the molecular group. A review of the
institutional database identified 58 out of 72 pediatric
patients who were operated for an MB at our department
between 1996 and 2020 that had a detailed operative report
and a surgical video as well as clinical and genetic
classification data available for analysis. The STO was
assessed based on intraoperative findings. Using the
intraoperatively defined STO, 'correct' prediction of
molecular groups was feasible in $20\%$ of WNT-MB, $60\%$ of
SHH-MB and $71\%$ of non-WNT/non-SHH MB. The positive
predictive values of the neurosurgical inspection to detect
the molecular group were 0.21 $(95\%$ CI 0.08-0.48) for
WNT-MB, 0.86 $(95\%$ CI 0.49-0.97) for SHH-MB and 0.73
$(95\%$ CI 0.57-0.85) for non-WNT/non-SHH MB. The present
study demonstrated a limited predictive value of the
intraoperatively observed STO for the prediction of the
molecular group of MB.},
keywords = {MB (Other) / molecular group (Other) / neurosurgery (Other)
/ origin (Other)},
cin = {B062 / HD01},
ddc = {610},
cid = {I:(DE-He78)B062-20160331 / I:(DE-He78)HD01-20160331},
pnm = {312 - Funktionelle und strukturelle Genomforschung
(POF4-312)},
pid = {G:(DE-HGF)POF4-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:37835571},
pmc = {pmc:PMC10571892},
doi = {10.3390/cancers15194877},
url = {https://inrepo02.dkfz.de/record/284754},
}