% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Telli:300101,
author = {T. Telli$^*$ and L. Lopes and M. Karpinski$^*$ and K. M.
Pabst$^*$ and V. Grünwald$^*$ and K. Shi and B.
Hadaschik$^*$ and C. Kesch$^*$ and L. Umutlu$^*$ and K.
Herrmann$^*$ and R. Seifert$^*$ and W. P. Fendler$^*$},
title = {{P}rognostic value of [18{F}]{FDG}- and {PSMA}-{PET} in
patients evaluated for [177{L}u]{L}u-{PSMA} therapy of
m{CRPC}.},
journal = {European journal of nuclear medicine and molecular imaging},
volume = {52},
issn = {1619-7070},
address = {Heidelberg [u.a.]},
publisher = {Springer-Verl.},
reportid = {DKFZ-2025-00601},
pages = {3199–3210},
year = {2025},
note = {Volume 52, pages 3199–3210, (2025)},
abstract = {To improve [177Lu]Lu-Prostate-specific membrane antigen
therapy (LuPSMA) selection, this study investigates the
prognostic value of PSMA and 2-[18F]fluoro-2-deoxy-D-glucose
([18F]FDG)-PET in metastatic castration-resistant prostate
cancer (mCRPC) patients considered for LuPSMA therapy.We
conducted a retrospective analysis in 152 mCRPC patients
referred for LuPSMA therapy who underwent PSMA and
[18F]FDG-PET/CT. Of these, 104 patients $(68.4\%)$ underwent
LuPSMA therapy, while 48 $(31.6\%)$ received other standard
of care (SOC). PET/CT analyses included visual assessment
and semiquantitative measurements. Clinical and laboratory
parameters were recorded. Overall survival (OS) and PSA
response (decline > $50\%)$ were primary and secondary
endpoints, respectively.Baseline [18F]FDG-derived total
tumor volume was the only independent predictor of overall
survival both in patients subsequently treated with LuPSMA
(HR 1.28 $[95\%CI$ 1.02-1.61]; p = 0.03) or in those under
other SOC (HR 1.61 $[95\%CI$ 1.02-2.56]; p = 0.04),
respectively. In other SOC patients, additional independent
predictors of OS were total lesion PSMA uptake (PSMA-TL; HR
1.14 $[95\%CI$ 1.03-1.26]; p = 0.01), [18F]FDG mean SUV (HR
20.88 $[95\%CI$ 1.2-364.74]; p = 0.04), and [18F]FDG total
lesion glycolysis (HR 1.61 $[95\%CI$ 1.02-2.56]; p = 0.04).
In LuPSMA patients, PSMA-PET SUVmean was a significant
independent predictor of PSA decline ≥ $50\%$ (OR 2.97
$[95\%CI$ 1.27-8.16]; p = 0.02).PSMA-PET and [18F]FDG-PET
provide imaging biomarkers of outcome in candidates for
LuPSMA. FDG-PET total tumor volume was an independent
predictor of overall survival in candidates for LuPSMA
therapy, irrespective of subsequent treatment decision.
PSMA-PET SUVmean was associated with biochemical response to
LuPSMA. Dual tracer imaging should further be assessed in
prospective trials for mCRPC treatment guidance.},
keywords = {Biomarkers (Other) / FDG (Other) / PSMA (Other) /
Prognostics (Other) / Prostate cancer (Other)},
cin = {ED01},
ddc = {610},
cid = {I:(DE-He78)ED01-20160331},
pnm = {899 - ohne Topic (POF4-899)},
pid = {G:(DE-HGF)POF4-899},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40113645},
doi = {10.1007/s00259-025-07198-y},
url = {https://inrepo02.dkfz.de/record/300101},
}