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Pretest PSA and Restaging PSMA PET/CT Predict Survival in Biochemically Recurrent Prostate Cancer

Affiliation
Cytel Incorporated, Waltam, MA 02452, USA
von Eyben, Rie;
ORCID
0000-0002-8867-5525
Affiliation
Institute for Preventive Medicine of German Armed Forces, 56626 Andernach, Germany
Hoffmann, Manuela Andrea;
ORCID
0000-0002-6199-8551
Affiliation
Department of Nuclear Medicine, University of Ankara, 0600 Ankara, Turkey;
Soydal, Cigdem;
ORCID
0000-0001-7097-6170
Affiliation
Department of Nuclear Medicine, University Hospital in Innsbruck, 6020 Innsbruck, Austria;
Virgolini, Irene;
ORCID
0000-0003-2352-3587
Affiliation
Department of Nuclear Medicine, Hacettepe University, Ankara 06230, Turkey
Tuncel, Murat;
ORCID
0000-0002-4882-9366
Affiliation
Department of Nuclear Medicine, Incept, Institute Holland, 38100 Grenoble, France;
Gauthé, Mathieu;
ORCID
0000-0002-3659-3253
Affiliation
Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA
Kapp, Daniel S.;
Affiliation
Center of Tobacco Control Research, DK-5230 Odense, Denmark
von Eyben, Finn Edler

Background: A biochemical recurrence (BCR) risk model was created based on pretest prostate specific antigen (PSA) and groupings by restaging prostate specific membrane antigen (PSMA) PET/CT. Methods: A cohort of 1216 BCR patients were analyzed for overall survival (OS) according to the PSA threshold and restaging PSMA PET/CT. A Cox regression analysis of OS was carried out to detect significant clinical characteristics. Results: In the cohort, 271 patients had a pretest PSA of <0.5 ng/mL and 945 patients had higher PSA values. The restaging PSMA PET/CT was positive for 834 patients and negative for 369. Of 1203 patients, 133 (11%) died, including 19 of the 369 (5%) patients without positive sites on the restaging PSMA PET/CT, 82 of the 711 (12%) with 1–5 positive sites, and 32 of the 123 (26%) with >5 positive sites. In the Cox regression analysis, four variables significantly predicted OS: treatment center, International Society of Urologic Pathology (ISUP) grade, pretest PSA threshold, and the grouping of positive sites on the restaging PSMA PET/CT. Conclusions: The pretest PSA and PSMA PET/CT were important for the OS of the BCR patients. The findings argue for the new BCR risk model and serve as framework for ongoing trials.

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