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
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.
Hivatkozás stílusok: IEEEACMAPAChicagoHarvardCSLMásolásNyomtatás
2025-04-03 11:24