Stage and Grade Migration in Prostate Cancer Treated With Radical Prostatectomy in a Large German Multicenter Cohort.


Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
04 2021
Historique:
received: 16 09 2020
revised: 27 12 2020
accepted: 27 12 2020
pubmed: 3 2 2021
medline: 10 8 2021
entrez: 2 2 2021
Statut: ppublish

Résumé

Overdiagnosis and overtherapy in prostate cancer (PCa) treatment should be avoided, which has led to an awareness of the need to decrease treatment in cases of low-risk PCa with radical prostatectomy (RP). Simultaneously, prostate-specific antigen testing has become less popular in the last few years, which has resulted in higher cancer grade and stage at diagnosis. We evaluated stage and grade migration in the disease of patients treated with RP in a large German cohort. Overall, 4842 patients undergoing RP between 2000 and 2019 were included. Age, prostate-specific antigen level, biopsy, and pathologic Gleason score as well as clinical and pathologic stage were collected. D'Amico risk groups and Gleason score were evaluated over different time points. We detected a significant grade migration toward higher grade. The proportion of biopsy Gleason sum ≤ 6 dropped from 45.8% to 20.6% between ≤ 2010 and 2017-2019. Further, the proportion of patients with low D'Amico risk scores also decreased by almost 50% (20.8% vs 12.2%). Finally, the proportion of non-organ-confined PCa increased over time, and the proportion of postoperative Gleason sum ≤ 6 decreased from 20% to 10% over time. Taken together, data indicate a significant preoperative grade and stage migration toward disease of higher grade in RP-treated PCa. Between the years 2000 and 2019, the proportion of biopsy Gleason sum ≤ 6 and the proportions of D'Amico low risk disease decreased by approximately 50% (respectively, 45% to 20% and 20.8% to 12.2%). This might indicate better patient selection for RP, but might also be a telltale sign of the rising mortality and morbidity of PCa.

Identifiants

pubmed: 33526328
pii: S1558-7673(21)00004-5
doi: 10.1016/j.clgc.2020.12.004
pii:
doi:

Substances chimiques

Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

162-166.e1

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Katharina Boehm (K)

GeSRU-Academics, Frankfurt, Germany; Department of Urology and Pediatric Urology, University Medical Center, Mainz, Germany. Electronic address: katharina.boehm@unimedizin-mainz.de.

Hendrik Borgmann (H)

GeSRU-Academics, Frankfurt, Germany; Department of Urology and Pediatric Urology, University Medical Center, Mainz, Germany.

Thomas Ebert (T)

URO-Cert eV, Berlin, Germany; Prostate center Metropolregion Nürnberg, Nürnberg, Germany.

Thomas Höfner (T)

GeSRU-Academics, Frankfurt, Germany; Department of Urology and Pediatric Urology, University Medical Center, Mainz, Germany.

Ehsan Khaljani (E)

URO-Cert eV, Berlin, Germany.

Marianne Schmid (M)

GeSRU-Academics, Frankfurt, Germany; Department of Urology, University Medical Center Göttingen, Göttingen, Germany.

Wolfgang Schulze-Seemann (W)

URO-Cert eV, Berlin, Germany; Prostate center Freiburg, Freiburg, Germany.

Peter Weib (P)

URO-Cert eV, Berlin, Germany; Kompetenznetz Prostata Siegen, Siegen, Germany.

Jan Herden (J)

URO-Cert eV, Berlin, Germany; Prostate center Cologne, Cologne, Germany; Department of Urology, University Hospital Cologne, Cologne, Germany.

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Classifications MeSH