% 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{Dietlein:874917,
author = {Dietlein, Felix and Hohberg, Melanie and Kobe, Carsten and
Zlatopolskiy, Boris D. and Krapf, Philipp and Endepols,
Heike and Täger, Philipp and Hammes, Jochen and
Heidenreich, Axel and Neumaier, Bernd and Drzezga, Alexander
and Dietlein, Markus},
title = {{A}n 18 {F}-{L}abeled {PSMA} {L}igand for {PET}/{CT} of
{P}rostate {C}ancer: {F}irst-in-{H}umans {O}bservational
{S}tudy and {C}linical {E}xperience with 18
{F}-{JK}-{PSMA}-7 {D}uring the {F}irst {Y}ear of
{A}pplication},
journal = {Journal of nuclear medicine},
volume = {61},
number = {2},
issn = {2159-662X},
address = {New York, NY},
publisher = {Soc.},
reportid = {FZJ-2020-01701},
pages = {202 - 209},
year = {2020},
abstract = {In preclinical trials, the recently developed tracer
2-methoxy-18F-DCFPyL (18F-JK-prostate-specific membrane
antigen [PSMA]-7) has shown favorable properties regarding
clinical performance and radiochemical accessibility. The
aim of this study was to evaluate the clinical utility of
18F-JK-PSMA-7 for PET/CT imaging of patients with prostate
cancer. Methods: In an Institutional Review Board–approved
pilot study, the initial clinical utility of PET/CT imaging
with 18F-JK-PSMA-7 was directly compared with 68Ga-PSMA-11
PET/CT in a group of 10 patients with prostate cancer. The 2
PSMA tracers were administered to each patient less than 3
wk apart. Next, we analyzed the data of 75 consecutive
patients who had undergone clinical 18F-JK-PSMA-7 PET/CT
imaging for tumor localization of biochemical recurrence
(BCR). Results: The pilot study in 10 patients who were
examined with both PSMA tracers demonstrated that
18F-JK-PSMA-7 was at least equivalent to 68Ga-PSMA-11. All
unequivocally 68Ga-PSMA-11–positive lesions could be also
detected using 18F-JK-PSMA-7, and in 4 patients additional
suspected PSMA-positive lesions were identified (1 patient
changed from PSMA-negative to PSMA-positive). In patients
with BCR (after prostatectomy or radiotherapy), the capacity
of 18F-JK-PSMA-7 PET/CT to detect at least one PSMA-positive
lesion was $84.8\%.$ The prostate-specific antigen
(PSA)–stratified detection rate of 18F-JK-PSMA-7 after
prostatectomy varied among $54.5\%$ (6/11 patients; PSA <
0.5 μg/L), $87.5\%$ (14/16 patients; PSA 0.5–2 μg/L),
and $90.9\%$ (20/22 patients; PSA > 2 μg/L). Conclusion:
The tracer 18F-JK-PSMA-7 was found to be safe and clinically
useful. We demonstrated that 18F-JK-PSMA-7 was not inferior
when directly compared with 68Ga-PSMA-11 in a pilot study
but indeed identified additional PSMA-avid suspected lesions
in oligometastasized patients with BCR. In a subsequent
analysis of a clinical cohort of BCR patients, 18F-JK-PSMA-7
was useful in tumor localization. 18F-JK-PSMA-7 is
recommended for future prospective trials.},
cin = {INM-5 / INM-2},
ddc = {610},
cid = {I:(DE-Juel1)INM-5-20090406 / I:(DE-Juel1)INM-2-20090406},
pnm = {573 - Neuroimaging (POF3-573)},
pid = {G:(DE-HGF)POF3-573},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:31324713},
UT = {WOS:000512119600013},
doi = {10.2967/jnumed.119.229542},
url = {https://juser.fz-juelich.de/record/874917},
}