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Role of Lutetium Radioligand Therapy in Prostate Cancer
Książek, I.
;
Ligęza, A.
;
Drzymała, F.
;
Borek, A.
;
Miszczyk, M. ✉
;
Francuz, M.R.
;
Matsukawa, A.
;
Yanagisawa, T.
;
Fazekas, T. [Fazekas, Tamás (Urológia), szerző] Urológiai Klinika (SE / AOK / K); Transzlációs Medicina Központ (SE / KSZE)
;
Zapała, Ł.
;
Rajwa, P. ✉
Angol nyelvű Összefoglaló cikk (Folyóiratcikk) Tudományos
Megjelent:
CANCERS 2072-6694
16
(13)
Paper: 2433
, 15 p.
2024
SJR Scopus - Oncology: Q1
Azonosítók
MTMT: 35144683
DOI:
10.3390/cancers16132433
WoS:
001269405400001
Scopus:
85198339775
PubMed:
39001495
Theranostics utilize ligands that chelate radionuclides and selectively bind with cancer-specific membrane antigens. In the case of prostate cancer (PCa), the state-of-the-art lutetium-177-PSMA combines the radioactive β-emitter 177Lu with Vipivotide Tetraxetan, a prostate-specific membrane antigen (PSMA)-binding ligand. Several studies have been conducted, and the therapy is not without adverse effects (e.g., xerostomia, nausea, and fatigue); however, few events are reported as severe. The available evidence supports the use of 177Lu-PSMA in selected metastatic castration-resistant prostate cancer patients, and the treatment is considered a standard of care in several clinical scenarios. Emerging research shows promising results in the setting of hormone-sensitive prostate cancer; however, evidence from high-quality controlled trials is still missing. In this review, we discuss the available evidence for the application of 177Lu-PSMA in the management of PCa patients. © 2024 by the authors.
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2025-04-03 11:24
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