Abstract

(1) Purpose: To investigate the role of 68Ga-PSMA-11 PET/CT in guiding retreatment stereotactic body radiation therapy (SBRT) in prostate cancer (PCa) patients in biochemical recurrence (BCR) after salvage radiotherapy (S-RT). (2) Methods: We retrospectively evaluated PCa patients previously treated with S-RT on the prostate bed and with proven serum prostate antigen (PSA) failure after S-RT. In all patients (pts), 68Ga-PSMA-11 PET/CT was positive in the prostate bed only and guided retreatment SBRT. All retreatments were performed by applying the same radiotherapy protocol (median dose of 18 Gy/3 fractions; IQR 18–21 Gy). The median follow-up was 27 months (range 4–35 months). (3) Results: 38 consecutive patients were considered in this analysis. The overall median PSA level before RT was 1.10 ng/mL (IQR 0.82–2.59). PSA decreased at 3 and 6 months after treatment, with a median value of 0.60 ng/mL (IQR 0.31–0.96; p < 0.001) and 0.51 ng/mL (IQR 0.29–1.17; p < 0.001), respectively. Overall, biochemical recurrence-free survival (b-RFS) was 15.0 months (95% CI 13–23). Grade-1 toxicity was reported in 31.6% of patients (12/38). (4) Conclusion: These results confirm that 68Ga-PSMA-11-PET/CT is able to identify the site of recurrence in patients who have failed S-RT, thus supporting the use of metastases-directed radiotherapy as a safe and effective treatment.

Highlights

  • Prostate cancer (PCa) is the most frequent malignancy in male patients [1]

  • The aim of this study is to investigate the role of 68 Ga-PSMA-11 PET/CT in guiding retreatment (SBRT) in prostate cancer (PCa) patients affected by prostate antigen (PSA) failure after salvage radiotherapy (S-RT)

  • 76 consecutive postsalvage biochemical recurrence (BCR) patients sent by the radiotherapy unit to perform 68 Ga-PSMA-11

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Summary

Introduction

Prostate cancer (PCa) is the most frequent malignancy in male patients [1]. Despite radical approaches such as prostatectomy and radiation therapy, 20–30% of PCa patients will develop a biochemical relapse (BCR) within 10 years from primary care, defined by progressively rising serum prostate antigen (PSA) levels [2]. Salvage radiation therapy to the prostatic bed and/or pelvic nodes can offer a chance for disease control at first BCR. Many patients treated with standard salvage radiation therapy experience PSA failure as a result of new recurrences of active disease; the mainstay for disease control in such patients is systemic therapy based on hormone blockade. In early BCR scenarios, namely, for serum PSA levels as low as 1.0 ng/mL, patients may harbor low burden disease within the pelvis and/or at a few extrapelvic sites, deemed to be treatable with local therapy when the site of recurrence is localized [4]

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