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Submitted
Abstract
Retrospective Review of the Diagnostic Performance of PSMA PET/CT versus mpMRI in the T staging of Clinically Significant Prostate Cancer
Podium Abstract
Basic Research
Oncology: Prostate
Author's Information
9
No more than 10 authors can be listed (as per the Good Publication Practice (GPP) Guidelines).
Please ensure the authors are listed in the right order.
Australia
Marco Rosario m.s.rosario@outlook.com Westmead Hospital Urology Sydney Australia *
Rowan Klein Nulend rowankleinnulend@hotmail.com Westmead Hospital Urology Sydney Australia -
Jeff Thomas Jeff.thomas@health.nsw.gov.au Westmead Hospital Nuclear Medicine Sydney Australia -
Chris Chen Chris.chen@health.nsw.gov.au Westmead Hospital Nuclear Medicine Sydney Australia -
Ali Atabaki Ali.Atabaki@health.nsw.gov.au Westmead Hospital Nuclear Medicine Sydney Australia -
Ankur Dhar Ankur.Dhar@health.nsw.gov.au Westmead Hospital Urology Sydney Australia -
Labib Rahman Labib.Rahman@health.nsw.gov.au Westmead Hospital Nuclear Medicine Sydney Australia -
Lawrence Kim lawrence.kim@health.nsw.gov.au Westmead Hospital Urology Sydney Australia -
Manish Patel manish.patel@health.nsw.gov.au Westmead Hospital Urology Sydney Australia -
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Abstract Content
Multiparametric MRI (mpMRI) is a well-established tool for pre-biopsy assessment in suspected prostate cancer. Prostate-specific membrane antigen positron emission tomography/computed tomography (PSMA PET/CT), while traditionally used for staging nodal and distant metastases, is emerging as a valuable modality in primary staging, including assessment of seminal vesicle invasion (SVI). However, comparative data between mpMRI and PSMA PET/CT in this context remain limited. This study assesses the diagnostic performance of mpMRI and PSMA PET/CT in predicting adverse pathological features in patients undergoing radical prostatectomy.
A retrospective analysis was conducted on patients who underwent radical prostatectomy between 2016 and 2024 under urologists within the Western Sydney Local Health District. Imaging findings from pre-operative mpMRI and PSMA PET/CT were compared with final histopathology. A positive mpMRI was defined as presence of a PI-RADS 3–5 lesion. Tumour characteristics including ISUP grade, cribriform architecture, intraductal features, SVI, and extra-prostatic extension (EPE) were evaluated. SUVmax was analysed in correlation with these features using Kruskal-Wallis and Mann-Whitney U tests.
A total of 240 patients were included (mean age: 67 years). PI-RADS 5 lesions were seen in 63% of cases. Histopathology most commonly revealed ISUP grade group 2 (52%), with 74% showing multifocal acinar adenocarcinoma, 18% intraductal carcinoma, and 2% ductal histology. Cribriform architecture was present in 53%, with EPE in 52% and SVI in 11% of cases. SUVmax was significantly higher in patients with ISUP grade group 5 (median 16.9 [IQR 9.6–22.1]) compared to groups 2 and 3 (p < 0.001), as well as in patients with EPE (9.7 vs 6.0, p < 0.001), SVI (13.0 vs 6.5, p < 0.001), and intraductal carcinoma (10.0 vs 6.4, p = 0.008). Cribriform architecture was not associated with significantly elevated SUVmax. Diagnostic performance for predicting SVI was highest with PSMA PET/CT (sensitivity 62%, specificity 95%), compared to mpMRI alone (sensitivity 19%, specificity 97%). Combining both modalities resulted in a sensitivity of 53% and specificity of 91%. Negative predictive values were high across all modalities (>90%).
Both mpMRI and PSMA PET/CT contribute valuable information in the primary staging of clinically significant prostate cancer. PSMA PET/CT demonstrates superior sensitivity in predicting SVI while maintaining high specificity, suggesting its growing role in pre-operative evaluation. Elevated SUVmax correlates strongly with higher-grade disease, EPE, SVI, and intraductal carcinoma. These findings support incorporating PSMA PET/CT into routine staging algorithms for high-risk prostate cancer patients.
 
 
 
 
 
 
 
 
 
 
 
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Presentation Details
Free Paper Podium(25): Oncology Prostate (F)
Aug. 17 (Sun.)
13:30 - 13:36
1