Utility of PSMA PET/CT for imaging ductal carcinoma of the prostate.

Authors

null

Ahmed M. Mahmoud

Mayo Clinic Rochester, Rochester, MN

Ahmed M. Mahmoud , Patrick Navin , Miguel Muniz , Fernando Quevedo , Jacob Orme , Jack R. Andrews , Adam McLain Kase , Osama M Mosalem , Alan Haruo Bryce , Irbaz Bin Riaz , Brian J. Burkett , Ayse T. Kendi , Geoffrey Johnson , Praful Ravi , Eugene D. Kwon , Oliver Sartor , Daniel S Childs

Organizations

Mayo Clinic Rochester, Rochester, MN, Department of Medical Oncology, Mayo Clinic, Rochester, MN, Mayo Clinic Arizona, Phoenix, AZ, Mayo Clinic Florida, Jacksonville, FL, Mayo Clinic Arizona, Scottsdale, AZ, Division of Hematology and Oncology, Mayo Clinic, Scottsdale, AZ, Dana-Farber Cancer Institute, Boston, MA

Research Funding

No funding sources reported

Background: Ductal carcinoma (DC) is the second most commonly encountered histologic variant of prostate cancer. Previous studies have described its molecular features and aggressive behavior, but few have explored the performance of PSMA PET/CT in the initial staging and follow-up of DC. Methods: To address this gap, we performed a single-institution retrospective analysis using the Mayo Clinic PSMA PET database. All patients receiving a PSMA PET/CT scan in the interval of January 1, 2021, to December 31, 2022, were eligible for inclusion. Cases were filtered and categorized by histology at the time of diagnosis to select for pure DAC and mixed ductal variants. Trained research personnel annotated disease- and treatment-related variables. A board-certified radiologist performed tumor burden segmentation with calculations of SUV max, total lesion SUV mean and volume, and total lesion uptake, and ascribed a miPSMA expression score. Results: We queried 1792 patients from our PSMA PET/CT registry and identified 32 (1.8%) patients with a pathologically confirmed DC, including 8 (25%) patients with pure ductal and 25 (75%) patients with mixed histology. The indication for PSMA PET/CT was biochemical progression or restaging for 29 (91%) patients and initial staging for 3 (9%) patients. The median (IQR) time from prostate cancer diagnosis to PSMA PET scan was 41.6 (11.5-64.7) months, during this time 50% (n= 16) of patients developed CRPC. At the time of the PSMA PET/CT scan, the median age was 70 years, the median (IQR) PSA was 0.5 ng/mL (0.2-2.6). The distribution of metastatic spread and quantitative imaging parameters from PSMA PET are shown in the Table. Conclusions: Despite low PSA at the time of imaging, PSMA PET/CT frequently detected high volume osseous and/or visceral metastases in patients with DC. However, it is noteworthy that more than 50% of patients with DC had a low miPSMA score (0-1). Additional studies are needed to better understand the performance of novel imaging modalities when evaluating variant prostate cancers.

FeaturesPure Ductal
(n=8)
Mixed Ductal
(n=24)
PSA at PSMA PET/CT scan (Median/IQR) ng/mL1.1
(0.06-4.23)
0.4
(0.20-2.38)
Distribution of disease
- Pelvic recurrence
- Distant lymph nodes
- Osseous
1-5 lesions
>5 lesions
- Visceral
Lung
Liver
Multiple

2 (25%)
4 (50%)
6 (75%)
4 (50%)
2 (25%)
3 (37.5%)
1 (12.5%)
0 (0%)
2 (25%)

11 (45.8%)
4 (16.7%)
8 (33.3%)
5 (20.8%)
3 (12.5%)
4 (16.7%)
4 (16.7%)
0 (0%)
0 (0%)
miPSMA score
0
1
2
3

1 (12.5%)
3 (37.5%)
2 (25%)
2 (25%)

0 (0%)
13 (54.2%)
9 (37.5%)
2 (8.3%)
Total tumor volume (Median/IQR)8.3 (1.1-193.4)1.9 (1.1-4.3)
SUV mean (Median/IQR)3.9 (1.5-6.5)3.3 (1.9-4.5)
SUV max (Median/IQR)6.6 (2.5-14.9)6.2 (2.5-8.9)

PSA: Prostate Specific Antigen, PSMA: Prostate Specific Membrane Antigen, CT: Computed Tomography, IQR: Interquartile Range, SUV: Standardized Uptake Value.

Disclaimer

This material on this page is ©2024 American Society of Clinical Oncology, all rights reserved. Licensing available upon request. For more information, please contact licensing@asco.org

Abstract Details

Meeting

2024 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session A: Prostate Cancer

Track

Prostate Cancer - Advanced,Prostate Cancer - Localized

Sub Track

Diagnostics and Imaging

Citation

J Clin Oncol 42, 2024 (suppl 4; abstr 49)

DOI

10.1200/JCO.2024.42.4_suppl.49

Abstract #

49

Poster Bd #

B6

Abstract Disclosures

Similar Abstracts

First Author: Edward Maldonado

First Author: Jose Mauricio Mota

First Author: Michael Leapman

First Author: Clayton P Smith