Back to Search Start Over

Clinical and Genomic Differences Between Advanced Molecular Imaging-detected and Conventional Imaging-detected Metachronous Oligometastatic Castration-sensitive Prostate Cancer.

Authors :
Sutera, Philip
Song, Yang
Van der Eecken, Kim
Shetty, Amol C.
English, Keara
Hodges, Theresa
Chang, Jinhee
Fonteyne, Valérie
Rana, Zaker
Ren, Lei
Mendes, Adrianna A.
Lumen, Nicolaas
Delrue, Louke
Verbeke, Sofie
De Man, Kathia
Song, Daniel Y.
Pienta, Kenneth
Feng, Felix Y.
Joniau, Steven
Lotan, Tamara
Source :
European Urology. Dec2023, Vol. 84 Issue 6, p531-535. 5p.
Publication Year :
2023

Abstract

We demonstrate that patients with oligometastatic castration-sensitive prostate cancer detected via molecular imaging alone have less aggressive disease, as indicated by fewer high-risk pathogenic DNA mutations, and better overall survival in comparison to patients with oligometastasis detected via conventional imaging. In metastatic castration-sensitive prostate cancer (mCSPC), disease volume plays an integral role in guiding treatment recommendations, including selection of docetaxel therapy, metastasis-directed therapy, and radiation to the prostate. Although there are multiple definitions of disease volume, they have commonly been studied in the context of metastases detected via conventional imaging (CIM). One such numeric definition of disease volume, termed oligometastasis, is heavily dependent on the sensitivity of the imaging modality. We performed an international multi-institutional retrospective review of men with metachronous oligometastatic CSPC (omCSPC), detected via either advanced molecular imaging alone (AMIM) or CIM. Patients were compared with respect to clinical and genomic features using the Mann-Whitney U test, Pearson's χ2 test, and Kaplan-Meier overall survival (OS) analyses with a log-rank test. A total of 295 patients were included for analysis. Patients with CIM-omCSPC had significantly higher Gleason grade group (p = 0.032), higher prostate-specific antigen at omCSPC diagnosis (8.0 vs 1.7 ng/ml; p < 0.001), more frequent pathogenic TP53 mutations (28% vs 17%; p = 0.030), and worse 10-yr OS (85% vs 100%; p < 0.001). This is the first report of clinical and biological differences between AMIM-detected and CIM-detected omCSPC. Our findings are particularly important for ongoing and planned clinical trials in omCSPC. Metastatic prostate cancer with just a few metastases only detected via newer scanning methods (called molecular imaging) is associated with fewer high-risk DNA mutations and better survival in comparison to metastatic cancer detected via conventional scan methods. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03022838
Volume :
84
Issue :
6
Database :
Academic Search Index
Journal :
European Urology
Publication Type :
Academic Journal
Accession number :
173608665
Full Text :
https://doi.org/10.1016/j.eururo.2023.04.025