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Salvage Androgen Deprivation Therapy as Potential Treatment for Recurrence after Robot-Assisted Radical Prostatectomy

Authors :
Hiroshi Kano
Yoshifumi Kadono
Renato Naito
Tomoyuki Makino
Hiroaki Iwamoto
Hiroshi Yaegashi
Shohei Kawaguchi
Takahiro Nohara
Kazuyoshi Shigehara
Kouji Izumi
Atsushi Mizokami
Source :
Cancers, Vol 16, Iss 7, p 1304 (2024)
Publication Year :
2024
Publisher :
MDPI AG, 2024.

Abstract

Background: The efficacy of intermittent androgen deprivation therapy (ADT) for biochemical recurrence (BCR) after robot-assisted radical prostatectomy (RARP) is unknown, and its usefulness in Japanese practice needs to be investigated. Methods: We conducted a retrospective analysis of 85 patients who underwent RARP and were selected for intermittent ADT for postoperative recurrence at Kanazawa University Hospital between 2009 and 2019. Intermittent ADT was administered for 2 years. If prostate-specific antigen levels increased post-treatment, intermittent ADT was reinitiated. The median follow-up period was 47 months. Results: The 73 patients had completed the initial course of ADT, and 12 were under initial ADT. The 5-year castration-resistant prostate-cancer-free survival rates, cancer-specific survival, and overall survival were 92.7%, 98.3%, and 94.7%, respectively. A subgroup analysis of 69 patients who completed intermittent ADT was conducted to evaluate the BCR rate following initial ADT. The 5-year BCR-free survival rate was 53.2%. Multivariate analysis identified testosterone ≤ 0.03 ng/mL during ADT as the sole predictor of BCR after ADT. Conclusions: Salvage intermittent ADT may be an effective treatment option for BCR after RARP. In addition, it would be useful to confirm strong testosterone suppression as a criterion for transition to intermittent therapy.

Details

Language :
English
ISSN :
20726694
Volume :
16
Issue :
7
Database :
Directory of Open Access Journals
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
edsdoj.7e697fd60bbf48d494fd733802939abb
Document Type :
article
Full Text :
https://doi.org/10.3390/cancers16071304