Biochemical recurrence after chemohormonal therapy followed by robot-assisted radical prostatectomy in very-high-risk prostate cancer patients.

Journal: Journal of robotic surgery
Published Date:

Abstract

Robot-assisted radical prostatectomy (RARP) has become one of the standard radical treatments for prostate cancer (PCa). A retrospective single-center cohort study was conducted on patients with PCa who underwent RARP at Gifu University Hospital between September 2017 and September 2022. In this study, patients were classified into three groups based on the National Comprehensive Cancer Network risk classification: low/intermediate-risk, high-risk, and very-high-risk groups. Patients with high- and very-high-risk PCa who were registered in the study received neoadjuvant chemohormonal therapy prior to RARP. Biochemical recurrence-free survival (BRFS) after RARP in patients with PCa was the primary endpoint of this study. The secondary endpoint was the relationship between biochemical recurrence (BCR) and clinical covariates. We enrolled 230 patients with PCa in our study, with a median follow-up of 17.0 months. When the time of follow-up was over, 19 patients (8.3%) had BCR, and the 2 years BRFS rate for the enrolled patients was 90.9%. Although there was no significant difference in BRFS between the low- and intermediate-risk group and the high/very-high-risk group, the 2 years BRFS rate was 100% in the high-risk group and 68.3% in the very-high-risk group (P = 0.0029). Multivariate analysis showed that positive surgical margins were a significant predictor of BCR in patients with PCa treated with RARP. Multimodal therapies may be necessary to improve the BCR in patients with very-high-risk PCa.

Authors

  • Fumiya Sugino
    Department of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
  • Keita Nakane
    Department of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
  • Makoto Kawase
    Department of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
  • Shota Ueda
    Department of Urology, Gifu Graduate School of Medicine, Gifu, Japan.
  • Masayuki Tomioka
    Department of Urology, Japanese Red Cross Takayama Hospital, Takayama 5068550, Japan.
  • Yasumichi Takeuchi
    Department of Urology, Gifu Graduate School of Medicine, Gifu, Japan.
  • Toyohiro Yamada
    Department of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
  • Sanae Namiki
    Department of Urology, Gifu Graduate School of Medicine, Gifu, Japan.
  • Naotaka Kumada
    Department of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
  • Kota Kawase
    Department of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
  • Daiki Kato
    Department of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
  • Manabu Takai
    Department of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
  • Koji Iinuma
    Department of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.
  • Yuki Tobisawa
    Department of Urology, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu, 501-1194, Japan.
  • Takayasu Ito
    Center for Clinical Training and Career Development, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Takuya Koie
    Department of Urology, Gifu University Graduate School of Medicine, Gifu 5011194, Japan.