Impact of Renin-Angiotensin System Inhibitors on Disease Characteristics in Patients with Localized Prostate Cancer Treated with Radical Prostatectomy: A European Association of Urology Young Academic Urologists Prostate Cancer Working Group Multi-institutional Study.

Cancer aggressiveness Prostate cancer Real-world evidence Renin-angiotensin system inhibitor

Journal

European urology open science
ISSN: 2666-1683
Titre abrégé: Eur Urol Open Sci
Pays: Netherlands
ID NLM: 101771568

Informations de publication

Date de publication:
Nov 2024
Historique:
accepted: 14 09 2024
medline: 21 10 2024
pubmed: 21 10 2024
entrez: 21 10 2024
Statut: epublish

Résumé

Collagen biosynthesis is intricately involved in the development and progression of solid tumors. Renin-angiotensin system inhibitors (RASi) impede TGF-β-mediated collagen synthesis in tumors by hindering activation of the angiotensin receptor. Our aim was to investigate a potential association between RASi use and the aggressiveness of prostate cancer (PCa). We conducted a retrospective multicenter analysis for a cohort of 1250 patients with PCa who underwent radical prostatectomy (RP) between 1990 and 2023 in four European high-volume centers. The study cohort comprised 625 RASi-treated patients and 625 age-matched RASi-naïve patients. Data for various parameters were collected, including age at RP, body mass index (BMI), prostate volume, prostate-specific antigen (PSA), percentage of free PSA, Gleason score (GS) at biopsy and RP, TNM stage, and the rate of biochemical recurrence (BCR). Clinical parameters for patients with and without RASi treatment were documented. Differences between the groups were compared using a Mann-Whitney U test and χ As expected, the RASi group had higher BMI levels than the RASi-naïve group ( Our findings indicate that RASi therapy does not have a significant effect on the biological aggressiveness of PCa. We analyzed data for 1250 patients with prostate cancer and found that the use of a commonly prescribed high blood pressure medication was not associated with a less aggressive form of localized prostate cancer.

Sections du résumé

Background and objective UNASSIGNED
Collagen biosynthesis is intricately involved in the development and progression of solid tumors. Renin-angiotensin system inhibitors (RASi) impede TGF-β-mediated collagen synthesis in tumors by hindering activation of the angiotensin receptor. Our aim was to investigate a potential association between RASi use and the aggressiveness of prostate cancer (PCa).
Methods UNASSIGNED
We conducted a retrospective multicenter analysis for a cohort of 1250 patients with PCa who underwent radical prostatectomy (RP) between 1990 and 2023 in four European high-volume centers. The study cohort comprised 625 RASi-treated patients and 625 age-matched RASi-naïve patients. Data for various parameters were collected, including age at RP, body mass index (BMI), prostate volume, prostate-specific antigen (PSA), percentage of free PSA, Gleason score (GS) at biopsy and RP, TNM stage, and the rate of biochemical recurrence (BCR). Clinical parameters for patients with and without RASi treatment were documented. Differences between the groups were compared using a Mann-Whitney U test and χ
Key findings and limitations UNASSIGNED
As expected, the RASi group had higher BMI levels than the RASi-naïve group (
Conclusions and clinical implications UNASSIGNED
Our findings indicate that RASi therapy does not have a significant effect on the biological aggressiveness of PCa.
Patient summary UNASSIGNED
We analyzed data for 1250 patients with prostate cancer and found that the use of a commonly prescribed high blood pressure medication was not associated with a less aggressive form of localized prostate cancer.

Identifiants

pubmed: 39430410
doi: 10.1016/j.euros.2024.09.005
pii: S2666-1683(24)00924-8
pmc: PMC11490865
doi:

Types de publication

Journal Article

Langues

eng

Pagination

105-111

Informations de copyright

© 2024 The Author(s).

Auteurs

Nastasiia Artamonova (N)

Department of Urology, Medical University Innsbruck, Innsbruck, Austria.

Mona Kafka (M)

Department of Urology, Medical University Innsbruck, Innsbruck, Austria.

Laura Faiss (L)

Department of Urology, Medical University Innsbruck, Innsbruck, Austria.

David Avetisyan (D)

UGC Urología, Hospital Universitario Virgen de las Nieves, Granada, Spain.

Ignacio Puche Sanz (I)

UGC Urología, Hospital Universitario Virgen de las Nieves, Granada, Spain.

Giulia La Bombarda (G)

Department of Urology, University of Padova, Padova, Italy.

Gennaio Iacono (G)

Department of Urology, University of Padova, Padova, Italy.

Fabio Zattoni (F)

Department of Urology, University of Padova, Padova, Italy.
Department of Medicine, University of Padova, Padua, Italy.

Eberhard Steiner (E)

Department of Urology, Medical University Innsbruck, Innsbruck, Austria.

Caroline D'Elia (C)

Department of Urology, Zentralkankenhaus Bozen, Bozen, Italy.

Armin Pycha (A)

Department of Urology, Zentralkankenhaus Bozen, Bozen, Italy.

Michael Ladurner (M)

Department of Urology, Medical University Innsbruck, Innsbruck, Austria.

Samed Jagodic (S)

Department of Urology, University of Tuzla, Tuzla, Bosnia and Herzegovina.

Giorgio Gandaglia (G)

Department of Urology, Urological Research Institute Vita-Salute University and San Raffaele Hospital, Milan, Italy.

Isabel Heidegger (I)

Department of Urology, Medical University Innsbruck, Innsbruck, Austria.

Classifications MeSH