UROLOGY / CLINICAL RESEARCH
Comparative analysis of prostate cancer grade at biopsy and radical prostatectomy: a retrospective observational study
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1
Department of Urology and Urological Oncology, Multidisciplinary Hospital in Warsaw-Miedzylesie, Warsaw, Poland
2
Department of Urology and Andrology, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland
3
Department of Urology, Institute of Medical Sciences, Faculty of Medicine, Collegium Medicum, Cardinal Stefan Wyszyński University in Warsaw, Warsaw, Poland
4
Department of Regenerative Medicine, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland
These authors had equal contribution to this work
Submission date: 2025-11-14
Final revision date: 2026-03-17
Acceptance date: 2026-03-20
Online publication date: 2026-06-04
Corresponding author
Jędrzej J. Skorupka
Department of Urology and Urological Oncology
Multidisciplinary Hospital in Warsaw-Miedzylesie
Bursztynowa 2
04-749 Warsaw, Poland,
Phone +48 22 47 35 149
KEYWORDS
TOPICS
ABSTRACT
Introduction:
Accurate Gleason grading is essential for optimal treatment selection in prostate cancer, particularly in patients eligible for active surveillance (AS). This study aimed to assess the rate of Gleason score upgrading after radical prostatectomy and its clinical implications in a large Polish cohort of patients with prostate cancer.
Material and methods:
The data of 534 men with localized prostate cancer treated with radical prostatectomy at two academic centers (2017–2024) were retrospectively analyzed. Gleason scores of preoperative biopsy specimens were compared with those of whole mount prostatectomy specimens. Statistical analyses included Wilcoxon signed rank, X2, Kendall’s t, and Cohen’s k tests.
Results:
Overall, Gleason scores were upgraded in 40% of the patients, downgraded in 10%, and concordant in 50%. Among the patients meeting AS criteria at diagnosis (clinical stage ≤ T2a, PSA level < 10 ng/ml, Gleason score 3 + 3 (ISUP 1), PSA density < 0.2 ng/ml/ml, and involvement of ≤ 2 cores), upgrading occurred in 58% and downgrading in 0%. International Society of Urological Pathology grading showed a similar pattern (upgrading in 41%, downgrading in 16%). Agreement between biopsy and prostatectomy grading was low (k ≈0.23).
Conclusions:
A high Gleason upgrading rate, especially among patients who met active surveillance eligibility criteria but ultimately underwent radical prostatectomy, indicates potential underestimation of biopsy grading in routine practice. Incorporating multiparametric magnetic resonance imaging with targeted biopsy and considering centralized pathology review may improve selection for AS and reduce undertreatment of clinically significant disease. These findings underscore the limitations of biopsy-based grading in routine clinical practice and highlight the need for cautious selection of patients for active surveillance.
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