Negative first follow-up prostate biopsy on active surveillance is associated with decreased risk of upgrading, suspicion of progression and converting to active treatment.


Journal

BJU international
ISSN: 1464-410X
Titre abrégé: BJU Int
Pays: England
ID NLM: 100886721

Informations de publication

Date de publication:
07 2021
Historique:
pubmed: 25 10 2020
medline: 15 12 2021
entrez: 24 10 2020
Statut: ppublish

Résumé

To determine the risk of disease progression and conversion to active treatment following a negative biopsy while on active surveillance (AS) for prostate cancer (PCa). Men on an AS programme at a single tertiary hospital (London, UK) between 2003 and 2018 with confirmed low-intermediate-risk PCa, Gleason Grade Group <3, clinical stage <T3 and a diagnostic prostate-specific antigen (PSA) level of <20 ng/mL. This cohort included men diagnosed by transrectal ultrasonography guided (12-14 cores) or transperineal (median 32 cores) biopsy. Multivariate Cox hazards regression analysis was undertaken to determine (i) risk of upgrading, (ii) clinical or radiological suspicion of disease progression, and (iii) transitioning to active treatment. Suspicion of disease progression was defined as any biopsy upgrading, >30% positive cores, magnetic resonance imaging (MRI) Likert score >3/T3 or PSA level of >20 ng/mL. Conversion to treatment included radical or hormonal treatment. Among the 460 eligible patients, 23% had negative follow-up biopsy findings. The median follow-up was 62 months, with one to two repeat biopsies and two MRIs per patient during that period. Negative biopsy findings at first repeat biopsy were associated with decreased risk of converting to active treatment (hazard ration [HR] 0.18, 95% confidence interval [CI] 0.09-0.37; P < 0.001), suspicion of disease progression (HR 0.56, 95% CI: 0.34-0.94; P = 0.029), and upgrading (HR 0.48, 95% CI 0.23-0.99; P = 0.047). Data are limited by fewer men with multiple follow-up biopsies. A negative biopsy finding at the first scheduled follow-up biopsy among men on AS for PCa was strongly associated with decreased risk of subsequent upgrading, clinical or radiological suspicion of disease progression, and conversion to active treatment. A less intense surveillance protocol should be considered for this cohort of patients.

Identifiants

pubmed: 33098158
doi: 10.1111/bju.15281
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

72-78

Informations de copyright

© 2020 The Authors BJU International © 2020 BJU International.

Références

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Auteurs

Sohail Singh (S)

School of Medical Education, Faculty of Life Sciences and Medicine, King's College London, London, UK.
The Urology Centre, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Preeti Sandhu (P)

School of Medical Education, Faculty of Life Sciences and Medicine, King's College London, London, UK.
The Urology Centre, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Kerri Beckmann (K)

Translational Oncology and Urology Research, Faculty of Life Sciences and Medicine, King's College London, London, UK.
University of South Australia Cancer Research Institute, University of South Australia, Adelaide, SA, Australia.

Aida Santaolalla (A)

Translational Oncology and Urology Research, Faculty of Life Sciences and Medicine, King's College London, London, UK.

Kamal Dewan (K)

School of Medical Education, Faculty of Life Sciences and Medicine, King's College London, London, UK.

Sharon Clovis (S)

The Urology Centre, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Jonah Rusere (J)

The Urology Centre, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Grace Zisengwe (G)

The Urology Centre, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Benjamin Challacombe (B)

The Urology Centre, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Christian Brown (C)

The Urology Centre, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Paul Cathcart (P)

The Urology Centre, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Rick Popert (R)

The Urology Centre, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Prokar Dasgupta (P)

The Urology Centre, Guy's and St Thomas' NHS Foundation Trust, London, UK.
School of Immunology and Microbial Sciences, Kings College London, London, UK.

Mieke Van Hemelrijck (M)

Translational Oncology and Urology Research, Faculty of Life Sciences and Medicine, King's College London, London, UK.

Oussama Elhage (O)

The Urology Centre, Guy's and St Thomas' NHS Foundation Trust, London, UK.
School of Immunology and Microbial Sciences, Kings College London, London, UK.

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