Prognosis of Gleason score 8 prostatic adenocarcinoma in needle biopsies: a nationwide population-based study.

Gleason grade Mortality Needle biopsy Prostate cancer

Journal

Virchows Archiv : an international journal of pathology
ISSN: 1432-2307
Titre abrégé: Virchows Arch
Pays: Germany
ID NLM: 9423843

Informations de publication

Date de publication:
29 Apr 2024
Historique:
received: 11 03 2024
accepted: 19 04 2024
revised: 09 04 2024
medline: 29 4 2024
pubmed: 29 4 2024
entrez: 29 4 2024
Statut: aheadofprint

Résumé

A 5-tier grouping of Gleason scores has recently been proposed. Studies have indicated prognostic heterogeneity within these groups. We assessed prostate cancer-specific mortality (PCSM) and all-cause mortality (ACM) for men diagnosed with Gleason score 3 + 5 = 8, 4 + 4 = 8 and 5 + 3 = 8 acinar adenocarcinoma on needle biopsy in a population-based national cohort. The Prostate Cancer data Base Sweden 5.0 was used for survival analysis with PCSM and ACM at 5 and 10 years as endpoints. Multivariable Cox regression models controlling for socioeconomic factors, stage and primary treatment type were used for PCSM and ACM. Among 199,620 men reported with prostate cancer in 2000-2020, 172,112 were diagnosed on needle biopsy. In 18,281 (11%), there was a Gleason score of 8 in needle biopsies, including a Gleason score of 3 + 5, 4 + 4 and 5 + 3 in 11%, 86% and 2.3%, respectively. The primary treatment was androgen deprivation therapy (55%), deferred treatment (8%), radical prostatectomy (16%) or radical radiotherapy (21%). PCSM in men with Gleason scores of 3 + 5, 4 + 4 and 5 + 3 at 5 years of follow-up was 0.10 (95% CI 0.09-0.12), 0.22 (0.22-0.23) and 0.32 (0.27-0.36), respectively, and at 10 years 0.19 (0.17-0.22), 0.34 (0.33-0.35) and 0.44 (0.39-0.49), respectively. There was a significantly higher PCSM after 5 and 10 years in men with Gleason score 5 + 3 cancers than in those with 4 + 4 and in Gleason score 4 + 4 cancers than in those with 3 + 5. Grouping of Gleason scores will eliminate the prognostic granularity of Gleason scoring, thus diminishing the prognostic significance of this proposed grading system.

Identifiants

pubmed: 38683251
doi: 10.1007/s00428-024-03810-y
pii: 10.1007/s00428-024-03810-y
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Wellcome Trust
ID : 204043
Pays : United Kingdom

Informations de copyright

© 2024. The Author(s).

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Auteurs

Lars Egevad (L)

Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital, 171 76, Stockholm, Sweden. lars.egevad@ki.se.

Chiara Micoli (C)

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

Brett Delahunt (B)

Department of Oncology-Pathology, Karolinska Institutet, Karolinska University Hospital, 171 76, Stockholm, Sweden.
Malaghan Institute of Medical Research, Wellington, New Zealand.

Hemamali Samaratunga (H)

Aquesta Uropathology and University of Queensland, Brisbane, QLD, Australia.

Andri Wilberg Orrason (AW)

Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.

Hans Garmo (H)

Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
Regional Cancer Centre Mid-Sweden, Uppsala University Hospital, Uppsala, Sweden.

Pär Stattin (P)

Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.

Martin Eklund (M)

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.

Classifications MeSH