Active Surveillance for Intermediate-Risk Prostate Cancer: Systematic Review and Meta-analysis of Current Protocols and Outcomes.


Journal

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

Informations de publication

Date de publication:
12 2020
Historique:
received: 27 02 2020
revised: 06 05 2020
accepted: 12 05 2020
pubmed: 10 8 2020
medline: 19 8 2021
entrez: 10 8 2020
Statut: ppublish

Résumé

Current guidelines allow active surveillance for intermediate-risk prostate cancer patients but do not provide comprehensive recommendations for selection. We performed a systematic review and meta-analysis of outcomes for active surveillance in intermediate- and low-risk groups. We performed a systematic literature search of intermediate-risk localized prostate cancer patients undergoing active surveillance using 3 literature search engines (Medline, Web of Science, and Scopus) over the past 10 years. The primary outcome was the percentage of patients who remain under surveillance. Secondary outcomes included cancer-specific survival, overall survival, and metastasis-free survival. For articles including both low- and intermediate-risk patients undergoing active surveillance, comparisons between the two groups were made. The proportion of patients who remained on active surveillance was comparable between the low- and intermediate-risk groups after 10 and 15 years' follow-up (odds ratio [OR], 0.97; 95% confidence interval [CI], 0.83-1.14; and OR, 0.86; 95% CI, 0.65-1.13). Cancer-specific survival was worse in the intermediate-risk group after 10 years (OR, 0.47; 95% CI, 0.31-0.69) and 15 years (OR, 0.34; 95% CI, 0.2-0.58). The overall survival rate showed no statistical difference at 5 years' follow-up (OR, 0.84; 95% CI, 0.45-1.57) but was worse in the intermediate-risk group after 10 years (OR, 0.43; 95% CI, 0.35-0.53). Metastases-free survival did not significantly differ after 5 years (OR, 0.55; 95% CI, 0.2-1.53) and was worse in the intermediate-risk group after 10 years (OR, 0.46; 95% CI, 0.28-0.77). Active surveillance could be offered to patients with intermediate-risk prostate cancer. However, they should be informed of the need for regular monitoring and the possibility of discontinuation as a result of a higher rate of progression. Available data indicate that 5-year survival rates between intermediate- and low-risk patients do not differ; 10-year survival rates are worse. To assess the long-term effectiveness and safety of active surveillance, it is necessary to develop unified algorithms for patient selection and management, and to prospectively conduct studies with long-term surveillance.

Identifiants

pubmed: 32768356
pii: S1558-7673(20)30116-6
doi: 10.1016/j.clgc.2020.05.008
pii:
doi:

Substances chimiques

Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

e739-e753

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Dmitry Enikeev (D)

Institute for Urology and Reproductive Health, Sechenov University, Moscow, Russia. Electronic address: dvenikeev@gmail.com.

Andrey Morozov (A)

Institute for Urology and Reproductive Health, Sechenov University, Moscow, Russia.

Mark Taratkin (M)

Institute for Urology and Reproductive Health, Sechenov University, Moscow, Russia.

Eric Barret (E)

Department of Urology, Institut Mutualiste Montsouris, Paris, France.

Vasiliy Kozlov (V)

Department of Public Health and Healthcare, Sechenov University, Moscow, Russia.

Nirmish Singla (N)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX.

Juan Gomez Rivas (JG)

Department of Urology, La Paz University Hospital, Madrid, Spain.

Alexey Podoinitsin (A)

Moscow Regional Research and Clinical Institute MONIKI n.a. M.F. Vladimirskiy, Moscow, Russia.

Vitaly Margulis (V)

Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX.

Petr Glybochko (P)

Institute for Urology and Reproductive Health, Sechenov University, Moscow, Russia.

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