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@ARTICLE{Ceccon:885860,
author = {Ceccon, G. and Lohmann, Philipp and Werner, Jan-Michael and
Caroline, Tscherpel and Dunkl, Veronika and Stoffels,
Gabriele and Rosen, Jurij and Rapp, Marion and Herrlinger,
Ulrich and Schäfer, Niklas and Shah, N. J. and Fink, Gereon
Rudolf and Langen, Karl-Josef and Galldiks, Norbert},
title = {{E}arly treatment response assessment using
$^{18}${F}-{FET} {PET} compared to contrast-enhanced {MRI}
in glioma patients after adjuvant temozolomide chemotherapy},
journal = {Journal of nuclear medicine},
volume = {62},
number = {7},
issn = {0022-3123},
address = {New York, NY},
publisher = {Soc.},
reportid = {FZJ-2020-04140},
pages = {918-925},
year = {2021},
abstract = {The goal of this study was to compare the value of
contrast-enhanced MRI and O-(2-[18F]fluoroethyl)-l-tyrosine
(18F-FET) PET for response assessment in glioma patients
after adjuvant temozolomide chemotherapy (TMZ). Methods:
After biopsy or resection and completion of radiotherapy
with concomitant TMZ, 41 newly diagnosed and
histomolecularly characterized glioma patients
(glioblastoma, $90\%;$ age range, 20–79 y) were
subsequently treated with adjuvant TMZ. MR and 18F-FET PET
imaging were performed at baseline and after the second
cycle of adjuvant TMZ. We obtained 18F-FET metabolic tumor
volumes (MTVs) as well as mean and maximum tumor-to-brain
ratios (TBRmean and TBRmax, respectively). Threshold values
of 18F-FET PET parameters to predict outcome were
established by receiver-operating-characteristic analyses
using a median progression-free survival (PFS) of ≥ 9 mo
and overall survival (OS) of ≥ 15 mo as reference. MRI
response assessment was based on the Response Assessment in
Neuro-Oncology (RANO) working group criteria. The predictive
value of changes of 18F-FET PET and MRI parameters on
survival was evaluated subsequently using univariate and
multivariate survival estimates. Results: After 2 cycles of
adjuvant TMZ chemotherapy, a treatment-induced reduction of
MTV and TBRmax predicted a significantly longer PFS and OS
(both P ≤ 0.03; univariate survival analyses) whereas RANO
criteria were not significant (P > 0.05). Multivariate
survival analysis revealed that TBRmax changes predicted a
prolonged PFS (P = 0.012) and changes of MTV a prolonged OS
(P = 0.005) independent of
O6-methylguanine-DNA-methyltransferase promoter methylation
and other strong prognostic factors. Conclusion: Changes of
18F-FET PET parameters appear to be helpful for identifying
responders to adjuvant TMZ early after treatment
initiation.},
cin = {INM-3 / INM-4},
ddc = {610},
cid = {I:(DE-Juel1)INM-3-20090406 / I:(DE-Juel1)INM-4-20090406},
pnm = {572 - (Dys-)function and Plasticity (POF3-572) / 5253 -
Neuroimaging (POF4-525)},
pid = {G:(DE-HGF)POF3-572 / G:(DE-HGF)POF4-5253},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:33158907},
UT = {WOS:000709477900011},
doi = {10.2967/jnumed.120.254243},
url = {https://juser.fz-juelich.de/record/885860},
}