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PSMA PET/CT Accuracy in Diagnosing Prostate Cancer Nodes Metastases.

Authors :
PEPE, PIETRO
PEPE, LUDOVICA
FIORENTINO, VINCENZO
CURDUMAN, MARA
PENNISI, MICHELE
FRAGGETTA, FILIPPO
Source :
In Vivo; Nov/Dec2024, Vol. 38 Issue 6, p2880-2885, 6p
Publication Year :
2024

Abstract

Background/Aim: This study aimed to evaluate the diagnostic accuracy of prostate-specific membrane antigen (PSMA)-directed positron emission tomography/ computed tomography (PET/CT) in pelvic nodal staging, using postoperative histopathology data as the reference standard. Patients and Methods: From January 2020 to June 2024, 78 patients with clinically significant prostate cancer (PCa) (ISUP Grade Group 2) underwent radical prostatectomy plus extended pelvic lymph node dissection (ePLND): 60 (77%) vs. 18 (23%) men had an intermediate vs. high risk PCa. All the patients underwent PSMA PET/TC before surgery for clinical staging and nodes focal uptake (standardized uptake value "SUVmax) was evaluated to rule out the presence of metastases. Results: PSMA PET/CT was suspicious for nodes metastases in 16/78 (20.5%) men (median SUVmax 26.2), conversely, histology demonstrated nodes metastases in 18/78 (23.1%). PSMA PET/CT was negative for nodal involvement in all Grade Group 2 (GG2) PCa, positive in 4/4 (100%) GG3 PCa, and in 10/14 (71.4%) GG5 PCa. In detail, PSMA PET/CT was false negative in 2/4 PCa, characterized by GG5 plus ductal adenocarcinoma. Overall, PSMA PET/CT sensitivity, specificity, positive and negative predictive value, and diagnostic accuracy in diagnosing nodal metastases were equal to 87.5, 96.8, 87.5 96.7, and 92.3%, respectively. Conclusion: PSMA PET/CT demonstrated an overall diagnostic accuracy of 92.3% in nodal staging (100% in GG2 PCa), which decreased to 63.6% in GG5 PCa. In high-risk patients or in case of ductal adenocarcinoma, a negative PSMA PET/CT does not rule out the need for ePLND. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0258851X
Volume :
38
Issue :
6
Database :
Complementary Index
Journal :
In Vivo
Publication Type :
Academic Journal
Accession number :
181050409
Full Text :
https://doi.org/10.21873/invivo.13769