Role of Lutetium Radioligand Therapy in Prostate Cancer

Author:

Książek Ignacy1,Ligęza Artur1,Drzymała Franciszek1,Borek Adam1,Miszczyk Marcin23ORCID,Francuz Marcin Radosław1,Matsukawa Akihiro24ORCID,Yanagisawa Takafumi4ORCID,Fazekas Tamás56,Zapała Łukasz7ORCID,Rajwa Paweł12

Affiliation:

1. Department of Urology, Medical University of Silesia, 41-800 Zabrze, Poland

2. Department of Urology, Medical University of Vienna, 1090 Vienna, Austria

3. Collegium Medicum—Faculty of Medicine, WSB University, 41-300 Dąbrowa Górnicza, Poland

4. Department of Urology, Jikei University School of Medicine, Tokyo 105-8461, Japan

5. Department of Urology, Semmelweis University, 1085 Budapest, Hungary

6. Centre for Translational Medicine, Semmelweis University, 1085 Budapest, Hungary

7. Clinic of General, Oncological and Functional Urology, Medical University of Warsaw, 02-091 Warsaw, Poland

Abstract

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.

Publisher

MDPI AG

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