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Updated: Sep 2, 2025

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Retzius-Sparing Robot-Assisted Radical Prostatectomy
Published on: May 19, 2022
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Prognostic differences among Grade Group 4 subgroups in robotic-assisted radical prostatectomy.
Takeshi Sasaki1, Shin Ebara2, Tomoyuki Tatenuma3
1Department of Nephro-Urologic Surgery and Andrology Mie University Graduate School of Medicine Tsu Japan.
BJUI Compass
|August 11, 2022
Summary
For prostate cancer patients undergoing robotic-assisted radical prostatectomy, specific Gleason scores within Grade Group 4 significantly impact recurrence risk. Pathological Gleason score 3+5 may be overestimated, highlighting the need to consider primary and secondary scores for accurate risk stratification.
Area of Science:
- Urologic Oncology
- Pathology
- Surgical Oncology
Background:
- The International Society of Urological Pathology (ISUP) Grade Group 4 (GG 4) is a critical prognostic category for prostate cancer (PCa).
- Subgroup analysis within GG 4 may refine risk stratification for patients undergoing treatment.
Purpose of the Study:
- To investigate oncological outcome differences among International Society of Urological Pathology Grade Group 4 (GG 4) subgroups in Japanese prostate cancer (PCa) patients.
- To determine if pathological Gleason scores (GS) of 3+5, 4+4, and 5+3 within GG 4 predict distinct biochemical recurrence (BCR) rates after robotic-assisted radical prostatectomy (RARP).
Main Methods:
- Retrospective multicentre cohort study of 298 Japanese PCa patients with GG 4 tumors undergoing RARP.
- Analysis of pre- and post-operative variables, focusing on biochemical recurrence (BCR)-free survival (BCRFS) across pathological GS subgroups (3+5, 4+4, 5+3).
- Multivariate analysis to identify independent risk factors for BCRFS.
Main Results:
- The 3-year BCRFS rate was 74.5% overall. Significant differences were observed among GG 4 subgroups: 93.8% for GS 3+5, 71.9% for GS 4+4, and 50.0% for GS 5+3 (P=0.01).
- Multivariate analysis identified pathological GS, PSA levels, pathological T and N stage, and surgical margins as independent risk factors for BCRFS.
- Patients with GS 4+4 and 5+3 had significantly higher BCR risk compared to GS 3+5.
Conclusions:
- Pathological Gleason score 4+4 and 5+3 are associated with worse BCRFS than 3+5 in localized PCa patients treated with RARP.
- Pathological GS 3+5 may be overestimated within the current GG 4 classification.
- Considering both primary and secondary Gleason scores is crucial for accurate BCR risk stratification after RARP.

