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@ARTICLE{Meiner:1010196,
author = {Meißner, Anna-Katharina and Gutsche, Robin and Galldiks,
Norbert and Kocher, Martin and Jünger, Stephanie T. and
Eich, Marie-Lisa and Nogova, Lucia and Araceli, Tommaso and
Schmidt, Nils Ole and Ruge, Maximilian I. and Goldbrunner,
Roland and Proescholdt, Martin and Grau, Stefan and Lohmann,
Philipp},
title = {{R}adiomics for the non-invasive prediction of {PD}-{L}1
expression in patients with brain metastases secondary to
non-small cell lung cancer},
journal = {Journal of neuro-oncology},
volume = {163},
number = {3},
issn = {0167-594x},
address = {Dordrecht [u.a.]},
publisher = {Springer Science + Business Media B.V},
reportid = {FZJ-2023-03007},
pages = {597 - 605},
year = {2023},
note = {„Open access publication funded by the Deutsche
Forschungsgemeinschaft (DFG, German Research Foundation) –
491111487“},
abstract = {BackgroundThe expression level of the programmed cell death
ligand 1 (PD-L1) appears to be a predictor for response to
immunotherapy using checkpoint inhibitors in patients with
non-small cell lung cancer (NSCLC). As differences in terms
of PD-L1 expression levels in the extracranial primary tumor
and the brain metastases may occur, a reliable method for
the non-invasive assessment of the intracranial PD-L1
expression is, therefore of clinical value. Here, we
evaluated the potential of radiomics for a non-invasive
prediction of PD-L1 expression in patients with brain
metastases secondary to NSCLC.Patients and
methodsFifty-three NSCLC patients with brain metastases from
two academic neuro-oncological centers (group 1, n = 36
patients; group 2, n = 17 patients) underwent tumor
resection with a subsequent immunohistochemical evaluation
of the PD-L1 expression. Brain metastases were manually
segmented on preoperative T1-weighted contrast-enhanced MRI.
Group 1 was used for model training and validation, group 2
for model testing. After image pre-processing and radiomics
feature extraction, a test-retest analysis was performed to
identify robust features prior to feature selection. The
radiomics model was trained and validated using random
stratified cross-validation. Finally, the best-performing
radiomics model was applied to the test data. Diagnostic
performance was evaluated using receiver operating
characteristic (ROC) analyses.ResultsAn intracranial PD-L1
expression (i.e., staining of at least $1\%$ or more of
tumor cells) was present in 18 of 36 patients $(50\%)$ in
group 1, and 7 of 17 patients $(41\%)$ in group 2.
Univariate analysis identified the contrast-enhancing tumor
volume as a significant predictor for PD-L1 expression (area
under the ROC curve (AUC), 0.77). A random forest classifier
using a four-parameter radiomics signature, including tumor
volume, yielded an AUC of 0.83 ± 0.18 in the training
data (group 1), and an AUC of 0.84 in the external test data
(group 2).ConclusionThe developed radiomics classifiers
allows for a non-invasive assessment of the intracranial
PD-L1 expression in patients with brain metastases secondary
to NSCLC with high accuracy.},
cin = {INM-3 / INM-4},
ddc = {610},
cid = {I:(DE-Juel1)INM-3-20090406 / I:(DE-Juel1)INM-4-20090406},
pnm = {5252 - Brain Dysfunction and Plasticity (POF4-525) / DFG
project 491111487 - Open-Access-Publikationskosten / 2022 -
2024 / Forschungszentrum Jülich (OAPKFZJ) (491111487)},
pid = {G:(DE-HGF)POF4-5252 / G:(GEPRIS)491111487},
typ = {PUB:(DE-HGF)16},
pubmed = {37382806},
UT = {WOS:001022079900002},
doi = {10.1007/s11060-023-04367-7},
url = {https://juser.fz-juelich.de/record/1010196},
}