Abstract
BACKGROUND AND OBJECTIVES: As a result of technical innovation, i.e., improvement of seed quality, implantation method, and dose calculation, it has been possible to continuously improve oncological results in the treatment of localized prostate cancer with low-dose-rate brachytherapy (LDR-BT). Randomized controlled trials have shown that there is no significant difference in oncological control between the use of radical prostatectomy and LDR-BT in patients with low-risk prostate cancer. The objective of this study was to investigate the oncological efficacy of LDR-BT. MATERIALS AND METHODS: A retrospective multicenter analysis was conducted on 618 patients treated with LDR-BT as monotherapy, who received a dose of 145 Gy. We used iodine(125) as the radioactive source. The analysis was conducted with follow-up data from two brachytherapy centers in Germany between 2004 and 2019. The primary endpoint was biochemical relapse-free survival (bRFS), whereby the Phoenix definition (PSA - nadir +2 ng/ml; PSA: prostate-specific antigen) was used to define biochemical relapse, i.e., therapeutic failure. RESULTS: Median follow-up was 52 months (range 3-180 months). The bRFS across all risk groups was 87.87%. Oncological efficacy was significantly higher in patients with a Gleason score of 6 and 7a (p-value < 0.0001); however, there was no significant difference in bRFS between these two groups. Bilateral tumor infiltration or prostate volume had no significant influence on bRFS. CONCLUSION: Our results show no difference in bRFS between Gleason score 6 and 7a.