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@ARTICLE{Kocher:892559,
author = {Kocher, Martin and Jockwitz, Christiane and Lohmann,
Philipp and Stoffels, Gabriele and Filss, Christian and
Mottaghy, Felix M. and Ruge, Maximilian I. and Weiss Lucas,
Carolin and Goldbrunner, Roland and Shah, N. J. and Fink,
Gereon R. and Galldiks, Norbert and Langen, Karl-Josef and
Caspers, Svenja},
title = {{L}esion-{F}unction {A}nalysis from {M}ultimodal {I}maging
and {N}ormative {B}rain {A}tlases for {P}rediction of
{C}ognitive {D}eficits in {G}lioma {P}atients},
journal = {Cancers},
volume = {13},
number = {10},
issn = {2072-6694},
address = {Basel},
publisher = {MDPI},
reportid = {FZJ-2021-02158},
pages = {2373 -},
year = {2021},
abstract = {Cognitive deficits are common in glioma patients following
multimodality therapy, but the relative impact of different
types and locations of treatment-related brain damage and
recurrent tumors on cognition is not well understood. In 121
WHO Grade III/IV glioma patients, structural MRI,
O-(2-[18F]fluoroethyl)-L-tyrosine FET-PET, and
neuropsychological testing were performed at a median
interval of 14 months (range, 1–214 months) after therapy
initiation. Resection cavities, T1-enhancing lesions,
T2/FLAIR hyperintensities, and FET-PET positive tumor sites
were semi-automatically segmented and elastically registered
to a normative, resting state (RS) fMRI-based functional
cortical network atlas and to the JHU atlas of white matter
(WM) tracts, and their influence on cognitive test scores
relative to a cohort of matched healthy subjects was
assessed. T2/FLAIR hyperintensities presumably caused by
radiation therapy covered more extensive brain areas than
the other lesion types and significantly impaired cognitive
performance in many domains when affecting left-hemispheric
RS-nodes and WM-tracts as opposed to brain tissue damage
caused by resection or recurrent tumors. Verbal episodic
memory proved to be especially vulnerable to T2/FLAIR
abnormalities affecting the nodes and tracts of the left
temporal lobe. In order to improve radiotherapy planning,
publicly available brain atlases, in conjunction with
elastic registration techniques, should be used, similar to
neuronavigation in neurosurgery.},
cin = {INM-4 / INM-11 / INM-1 / INM-3 / JARA-BRAIN},
ddc = {610},
cid = {I:(DE-Juel1)INM-4-20090406 / I:(DE-Juel1)INM-11-20170113 /
I:(DE-Juel1)INM-1-20090406 / I:(DE-Juel1)INM-3-20090406 /
I:(DE-Juel1)VDB1046},
pnm = {525 - Decoding Brain Organization and Dysfunction
(POF4-525) / HBP SGA3 - Human Brain Project Specific Grant
Agreement 3 (945539)},
pid = {G:(DE-HGF)POF4-525 / G:(EU-Grant)945539},
typ = {PUB:(DE-HGF)16},
pubmed = {34069074},
UT = {WOS:000654648600001},
doi = {10.3390/cancers13102373},
url = {https://juser.fz-juelich.de/record/892559},
}