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@INPROCEEDINGS{Peplinski:1053904,
author = {Peplinski, Jana-Marie and Werner, Jan-Michael and Ceccon,
Garry and Wollring, Michael and Stetter, Isabelle and Rosen,
Jurij and Rosen, Elena and Kraft, Manuel and Fink, Gereon
and Langen, Karl-Josef and Lohmann, Philipp and Galldiks,
Norbert},
title = {{IMG}-61. {A}ssessment of18{F}-{FET} {PET}-based response
to bevacizumab-based regimens in patients with glioblastoma
at relapse using the {PET} {RANO} 1.0 criteria},
issn = {1523-5866},
reportid = {FZJ-2026-01602},
year = {2025},
abstract = {AbstractBACKGROUNDWe evaluated the amino acid PET-based
response assessment criteria (PET RANO 1.0) for their
ability to predict longer overall survival (OS) in patients
with glioblastoma treated with bevacizumab-based regimens at
relapse.PATIENTS AND METHODSThirty-eight adult patients with
IDH-wildtype glioblastoma were identified from three
previously published studies. All patients (i) received
bevacizumab in combination with a second agent (irinotecan,
lomustine, or nivolumab), (ii) underwent MRI- and
O-(2-[18F]fluoroethyl)-L-tyrosine (FET) PET imaging at
baseline and at a median time of 8 weeks (range, 4-12 weeks)
after treatment initiation, and (iii) had available
PET-derived parameters, i.e., metabolic tumor volume (MTV),
maximum and mean tumor-to-brain ratios (TBRmax and TBRmean).
A post-hoc analysis was performed to evaluate the predictive
value of the PET RANO 1.0 criteria. In addition, ROC
analyses were performed to define PET parameter thresholds
for predicting an OS≥9 months. Furthermore, response
prediction using the RANO 2.0 criteria for MRI was compared
with the PET RANO 1.0 criteria.RESULTSAccording to the PET
RANO 1.0 criteria, patients fulfilling the criterion Stable
Disease (n=10), Partial Response (n=19), or Complete
Response (n=1) had a significantly longer OS than patients
with Progressive Disease (n=8) (9.0 vs. 4.0 months;
P=0.001). Among the suggested thresholds by the PET RANO 1.0
criteria, only a MTV reduction $≥40\%$ was significantly
predictive of response (7.3 vs. 4.0 months; P=0.008).
Optimal thresholds identified by ROC analysis differed from
those proposed by the PET RANO 1.0 criteria. A reduction in
MTV by $≥30\%$ and in TBRmean by $≥4\%$ were both
predictive of longer OS (7.3 vs. 4.0 months; P=0.008, and
10.6 vs. 6.0 months; P=0.010, respectively). The RANO 2.0
criteria were less significant to predict a longer OS (9.0
vs. 6.0 months; P=0.015).CONCLUSIONPET RANO 1.0 criteria
appear to be effective in predicting response to
bevacizumab-based therapy in glioblastomas at relapse.},
month = {Nov},
date = {2025-11-20},
organization = {7th Quadrennial Meeting of the World
Federation of Neuro-Oncology Societies,
Honolulu (USA), 20 Nov 2025 - 23 Nov
2025},
cin = {INM-4},
ddc = {610},
cid = {I:(DE-Juel1)INM-4-20090406},
pnm = {5253 - Neuroimaging (POF4-525)},
pid = {G:(DE-HGF)POF4-5253},
typ = {PUB:(DE-HGF)1},
doi = {10.1093/neuonc/noaf201.1140},
url = {https://juser.fz-juelich.de/record/1053904},
}