Cohort study of oligorecurrent prostate cancer patients: Oncological outcomes of patients treated with salvage lymph node dissection via PSMA radioguided surgery.

Authors

null

Tobias Maurer

Martini-Klinik Prostate Cancer Center, University Hospital Hamburg-Eppendorf, Hamburg, Germany

Tobias Maurer , Mehrdad Mehdi Irai , Isabel Rauscher , Ricarda Simon , Matthias Eiber , Fijs WB van Leeuwen , Pim van Leeuwen , Lars Budaeus , Thomas Steuber , Markus Graefen , Pierre Tennstedt , Matthias Heck , Thomas Horn , Sophie Knipper

Organizations

Martini-Klinik Prostate Cancer Center, University Hospital Hamburg-Eppendorf, Hamburg, Germany, Martini-Klinik, Hamburg, Germany, Department of Nuclear Medicine, Technical University Munich, Munich, Germany, Department of Urology, Technical University of Munich, Munich, Germany, Leiden University Medical Center, Leiden, Netherlands, Department of Urology, Antoni van Leeuwenhoek Hospital – the Netherlands Cancer Institute, Amsterdam, Netherlands, Martini-Klinik, University Medical Center Hamburg-Eppendorf, Hamburg, Germany, University Medical Center Hamburg-Eppendorf, Martini-Klinik, Hamburg, Germany, Department of Urology, Klinikum rechts der Isar, TU München, Munich, Germany, Rechts der Isar University Hospital, Technical University of Munich, Munich, Germany, Martini-Klinik Prostate Cancer Center, Hamburg, Germany

Research Funding

No funding received

Background: Prostate-specific membrane antigen (PSMA) positron-emission tomography (PET) allows detection of small and/or atypically localized metastatic prostate cancer (PCa) lesions. In a subset of patients with recurrent oligometastatic PCa salvage surgery with PSMA-targeted radioguidance (PSMA-RGS) may be of value. We aimed to evaluate the oncological outcomes of salvage PSMA-RGS for oligorecurrent PCa and determine predictive preoperative factors of improved outcomes. Methods: In this cohort study within two tertiary care centers, patients with biochemical recurrence (BCR) after radical prostatectomy (RP) and imaging with PSMA PET receiving salvage PSMA-RGS between 2014 and 2020 were analyzed. Kaplan-Meier and multivariable Cox regression models adjusted for various parameters were used to test for BCR-free survival (BFS) and therapy-free survival (TFS) differences. Postoperative complications were classified according to Clavien-Dindo. Results: Overall, 364 patients were assessed. At PSMA-RGS, median (IQR) age and preoperative PSA was 67 (61-71) years and 1.0 (0.5-1.9) ng/ml. Metastatic soft-tissue lesions were removed in 356 (94.4%) patients. Within three months from surgery, 25 (6.6%) patients suffered from Clavien-Dindo complications grade III-IV. During follow-up, 235 patients experienced BCR and 129 patients received further therapy. Median follow-up for patients who did not experience BCR and who did not receive further therapy was 11.1 months and 10.5 months, respectively. Median (IQR) BFS and TFS was 7.8 (5.4-10.9) and 34.9 (24.7-43.5) months. At two years of follow-up, BFS rate was 31.9% and TFS rate was 56.6%. In multivariable analyses, higher preoperative PSA (HR: 1.06), higher number of PSMA-avid lesions on preoperative imaging (HR: 1.2) and multiple (pelvic plus retroperitoneal) localizations (HR: 1.7), as well as retroperitoneal localization (HR: 2.0) of lesions in PSMA PET imaging were independent predictors of BCR after PSMA-RGS. Limitations are the retrospective design and lack of a control group. Conclusions: As salvage surgery in oligorecurrent PCa currently constitutes an experimental treatment approach careful patient selection is mandatory based on life expectancy, low PSA values and low number of PSMA PET avid lesions located in the pelvis. Further studies are needed to confirm our findings and define the oncological value of salvage surgical procedures in oligorecurrent PCa.

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Abstract Details

Meeting

2022 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session A: Prostate Cancer

Track

Prostate Cancer - Advanced,Prostate Cancer - Localized

Sub Track

Therapeutics

Citation

J Clin Oncol 40, 2022 (suppl 6; abstr 106)

DOI

10.1200/JCO.2022.40.6_suppl.106

Abstract #

106

Poster Bd #

Online Only

Abstract Disclosures