CC BY 4.0 · World J Nucl Med 2023; 22(02): 152-170
DOI: 10.1055/s-0043-1769965
Presentation Abstracts

177Lu-PSMA-617 in the Treatment of Castration-Resistant Prostate Cancer: Experience in Uruguay

Helen Silva
1   Urology Center, Clínical Hospital “Dr. Manuel Quintela,” Montevideo, Uruguay
,
Enzo Silvera
2   Uruguayan Center of Molecular Imaging – CUDIM, Uruguay
,
Agustina Banchero
2   Uruguayan Center of Molecular Imaging – CUDIM, Uruguay
,
Ismael Cordero
2   Uruguayan Center of Molecular Imaging – CUDIM, Uruguay
,
Omar Alonso
2   Uruguayan Center of Molecular Imaging – CUDIM, Uruguay
,
Pablo Duarte
2   Uruguayan Center of Molecular Imaging – CUDIM, Uruguay
,
Juan Pablo Gambini
2   Uruguayan Center of Molecular Imaging – CUDIM, Uruguay
,
Gerardo dos Santos
2   Uruguayan Center of Molecular Imaging – CUDIM, Uruguay
› Author Affiliations
 

erardo.dossantos@cudim.org

Introduction: Prostate cancer is the most frequent solid neoplasm in the world, ranking first in incidence and mortality in Uruguayan men. Despite recent therapeutic advances, metastatic-Castration-Resistant-Prostate-Cancer (mCRPC) remains invariably fatal. Long before 177Lutetium-PSMA radio-directed therapy was approved by the FDA (03/2022), Uruguay already had this technology available for this group of patients. To assess the therapeutic response and safety profile of 177Lu-PSMA-617 in the treatment of mCRPC-patients.

Methods: Prospective, analytical and experimental study of mCRPC patients who underwent doses of 177Lu-PSMA-617 (7.4GBq every 6 weeks) at CUDIM in the period October 2017/June 2022.

We included 24 PET/CT-PSMA-positive patients who received at least one new androgen-axis drug and 1 or 2 taxane regimens. 68Ga-PSMA-11 PET/CT was performed periodically assessing PSMA expression in metastatic lesions and response. Primary end-point was the therapeutic response in terms of imaging tumor volume. Biochemical response, clinical response (visual analog pain scale, VS) and adverse events (Clavien–Dindo Scale) were assessed as secondary end-points.

Results: In total, 80% of patients completed at least 3 cycles of 177Lu-PSMA-617. Five patients completed 4 cycles and 1 completed 5 cycles due to high response rate. In addition, 44% presented a positive response regarding decreased tumor volume, measured in all cases by PET/CT. A total of 63% showed a positive biochemical response (PSA decrease). 75% of patients with metastatic debut did not respond to therapy and 100% of patients with Gleason score of 8 or more progressed after the third cycle. There were no cases of hepatotoxicity or nephrotoxicity. 55% reported sustained pain relief after treatment.

Conclusion: 177Lu-PSMA-617 therapy is a promising option in the treatment of patients with mCRPC, whose survival and quality of life have not been able to improve despite the innumerable treatments available. Carrying out a longer follow-up to confirm encouraging data on prolongation of overall survival and imaging relapse-free survival is mandatory.



Publication History

Article published online:
25 May 2023

© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

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