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@ARTICLE{Hennrich:182301,
author = {U. Hennrich$^*$ and M. Eder$^*$},
title = {[177{L}u]{L}u-{PSMA}-617 ({P}luvicto{TM}): {T}he {F}irst
{FDA}-{A}pproved {R}adiotherapeutical for {T}reatment of
{P}rostate {C}ancer.},
journal = {Pharmaceuticals},
volume = {15},
number = {10},
issn = {1424-8247},
address = {Basel},
publisher = {MDPI},
reportid = {DKFZ-2022-02558},
pages = {1292},
year = {2022},
note = {#EA:W630#},
abstract = {In March 2022, [177Lu]Lu-PSMA-617 (PluvictoTM) was approved
by the FDA for the treatment of prostate cancer patients.
Until now, the approval has been limited to patients with
PSMA-positive metastatic castration-resistant prostate
cancer who have previously received other therapy options
(such as inhibition of the androgen receptor pathway and
taxane-based chemotherapy). [177Lu]Lu-PSMA-617, which
combines a PSMA-specific peptidomimetic with a therapeutical
radionuclide, is used in a radioligand therapy that
selectively delivers ionizing radiation to tumor cells,
causing their death, while sparing the surrounding healthy
tissue. In numerous clinical trials, the efficacy of
[177Lu]Lu-PSMA-617 was demonstrated.},
subtyp = {Review Article},
keywords = {PSMA (Other) / PluvictoTM (Other) / [177Lu]Lu-PSMA-617
(Other) / prostate cancer (Other) / radioligand therapy
(RLT) (Other) / theranostics (Other)},
cin = {W630 / FR01},
ddc = {610},
cid = {I:(DE-He78)W630-20160331 / I:(DE-He78)FR01-20160331},
pnm = {315 - Bildgebung und Radioonkologie (POF4-315)},
pid = {G:(DE-HGF)POF4-315},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:36297404},
doi = {10.3390/ph15101292},
url = {https://inrepo02.dkfz.de/record/182301},
}