Long-term outcomes of active surveillance for clinically localized prostate cancer in a community-based setting: results from a prospective non-interventional study.


Journal

World journal of urology
ISSN: 1433-8726
Titre abrégé: World J Urol
Pays: Germany
ID NLM: 8307716

Informations de publication

Date de publication:
Jul 2021
Historique:
received: 23 06 2020
accepted: 21 09 2020
pubmed: 2 10 2020
medline: 12 1 2022
entrez: 1 10 2020
Statut: ppublish

Résumé

To report on long-term outcomes of patients treated with active surveillance (AS) for localized prostate cancer (PCa) in the daily routine setting. HAROW (2008-2013) was a non-interventional, health service research study about the management of localized PCa in the community setting, with 86% of the study centers being office-based urologists. A follow-up examination of all patients who opted for AS as primary treatment was carried out. Overall, cancer-specific, and metastasis-free survival, as well as discontinuation rates, were determined. Of 329 patients, 62.9% had very-low- and 21.3% low-risk tumours. The median follow-up was 7.7 years (IQR 4.7-9.1). Twenty-eight patients (8.5%) died unrelated to PCa, of whom 19 were under AS or watchful waiting (WW). Additionally, seven patients (2.1%) developed metastasis. The estimated 10-year overall and metastasis-free survival was 86% (95% CI 81.7-90.3) and 97% (95% CI 94.6-99.3), respectively. One hundred eighty-seven patients (56.8%) discontinued AS changing to invasive treatment: 104 radical prostatectomies (RP), 55 radiotherapies (RT), and 28 hormonal treatments (HT). Another 50 patients switched to WW. Finally, 37.4% remained alive without invasive therapy (22.2% AS and 15.2% WW). Intervention-free survival differed between the risk groups: 47.8% in the very-low-, 33.8% in the low- and 34.6% in the intermediate-/high-risk-group (p = 0.008). On multivariable analysis, PSA-density ≥ 0.2 ng/ml Even in routine care, AS can be considered a safe treatment option. Our results might encourage office-based urologists regarding the implementation of AS and to counteract possible concerns against this treatment option.

Identifiants

pubmed: 33000341
doi: 10.1007/s00345-020-03471-x
pii: 10.1007/s00345-020-03471-x
pmc: PMC8332563
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2515-2523

Informations de copyright

© 2020. The Author(s).

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Auteurs

Jan Herden (J)

University of Cologne, Faculty of Medicine and University Hospital Cologne, Department of Urology, Uro-Oncology, Robot-Assisted and Reconstructive Urology, Cologne, Germany. jan.herden@uk-koeln.de.
PAN Clinic, Urological Practice, Cologne, Germany. jan.herden@uk-koeln.de.

Andreas Schwarte (A)

Urological Practice Borken, Borken, Germany.
Department of Urology, St. Agnes Hospital Bocholt, Bocholt, Germany.

Thorsten Werner (T)

Urological Practice Herzberg, Herzberg Am Harz, Germany.

Uwe Behrendt (U)

Urological Practice Wittenbergplatz, Berlin, Germany.

Axel Heidenreich (A)

University of Cologne, Faculty of Medicine and University Hospital Cologne, Department of Urology, Uro-Oncology, Robot-Assisted and Reconstructive Urology, Cologne, Germany.

Lothar Weissbach (L)

Health Research for Men GmbH, Berlin, Germany.

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Classifications MeSH