Abstract

BackgroundA substantial number of patients will develop further biochemical progression after radical prostatectomy (RP) and salvage radiotherapy (sRT). Recently published data using prostate-specific membrane antigen ligand positron emission tomography (PSMA - PET) for re-staging suggest that those recurrences are often located outside the prostate fossa and most of the patients have a limited number of metastases, making them amenable to metastasis-directed treatment (MDT).MethodsWe analyzed 78 patients with biochemical progression after RP and sRT from a retrospective European multicenter database and assessed the biochemical recurrence-free survival (bRFS; PSA < nadir + 0.2 ng/ml or no PSA decline) as well as the androgen deprivation therapy- free survival (ADT-FS) using Kaplan-Meier curves. Log-rank test and multivariate analysis was performed to determine influencing factors.ResultsA total of 185 PSMA – PET positive metastases were detected and all lesions were treated with radiotherapy (RT). Concurrent ADT was prescribed in 16.7% (13/78) of patients. The median PSA level before RT was 1.90 ng/mL (range, 0.1–22.1) and decreased statistically significantly to a median PSA nadir level of 0.26 ng/mL (range, 0.0–12.25; p < 0.001). The median PSA level of 0.88 ng/mL (range, 0.0–25.8) at the last follow-up was also statistically significantly lower (p = 0.008) than the median PSA level of 1.9 ng/mL (range, 0.1–22.1) before RT. The median bRFS was 17.0 months (95% CI, 14.2–19.8). After 12 months, 55.3% of patients were free of biochemical progression. Multivariate analyses showed that concurrent ADT was the most important independent factor for bRFS (p = 0.01). The median ADT-FS was not reached and exploratory statistical analyses estimated a median ADT-FS of 34.0 months (95% CI, 16.3–51.7). Multivariate analyses revealed no significant parameters for ADT-FS.ConclusionsRT as MDT based on PSMA - PET of all metastases of recurrent prostate cancer after RP and sRT represents a viable treatment option for well-informed and well-selected patients.

Highlights

  • A substantial number of patients will develop further biochemical progression after radical prostatectomy (RP) and salvage radiotherapy

  • Recent data showed a positive effect on the clinical outcome for metastasis-directed treatment (MDT) with low toxicity, staging with positron emission tomography (PET) with prostatespecific membrane antigen (PSMA) radio ligands was not available and the number of metastases could be underestimated [10, 11]

  • Concurrent Androgen deprivation therapy (ADT) was prescribed in 16.7% (13/78) of patients and ADT was deferred in the remaining patients

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Summary

Introduction

A substantial number of patients will develop further biochemical progression after radical prostatectomy (RP) and salvage radiotherapy (sRT). Published data using prostate-specific membrane antigen ligand positron emission tomography (PSMA - PET) for re-staging suggest that those recurrences are often located outside the prostate fossa and most of the patients have a limited number of metastases, making them amenable to metastasis-directed treatment (MDT). Published data suggest that early recurrences are often located outside the prostate fossa [4,5,6], and a large proportion of these patients (40–70%) have a limited number of metastases, making them amenable to metastasis-directed treatment (MDT) [7]. These cases are usually considered oligorecurrent disease. Recent data showed a positive effect on the clinical outcome for MDT with low toxicity, staging with positron emission tomography (PET) with prostatespecific membrane antigen (PSMA) radio ligands was not available and the number of metastases could be underestimated [10, 11]

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