Evidence map›Paper›PMID 36008540›Full record

ArticleProstate cancer and prostatic diseases2023

Risk of progression following a negative biopsy in prostate cancer active surveillance.

Kerri Beckmann, Aida Santaolalla, Mikio Sugimoto, Peter Carroll, Jose Rubio, Arnauld Villers, Anders Bjartell, Todd Morgan, Prokar Dasgupta, Mieke Van Hemelrijck and 2 more

Abstract read
In one paragraph

Article in Prostate cancer and prostatic diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Kerri BeckmannCancer Epidemiology and Population Health Research Group, University of South Australia, Adelaide, Australia. Kerri.beckmann@unisa.edu.au.ORCID 0000-0002-9798-1479
Aida SantaolallaTranslational Oncology and Urology Research, Kings College London, London, UK.
Mikio SugimotoFaculty of Medicine, Kagawa University, Kagawa, Japan.ORCID 0000-0001-9266-782X
Peter CarrollDepartment of Urology, UCSF-Helen Diller Comprehensive Cancer Centre, University of California San Francisco, San Francisco, CA, USA.
Jose RubioInstituto Valenciano de Oncologia, Valencia, Spain.
Arnauld VillersLille University Hospital Center, Lille, France.
Anders BjartellDepartment of Urology, Skane University Hospital, Malmo, Sweden.ORCID 0000-0002-5761-3786
Todd MorganUniversity of Michigan and Michigan Urological Surgery Improvement Collaborative, Michigan, MI, USA.ORCID 0000-0002-1140-0603
Prokar DasguptaGuy's and St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0001-8690-0445
Mieke Van HemelrijckTranslational Oncology and Urology Research, Kings College London, London, UK.
Oussama ElhageGuy's and St Thomas' NHS Foundation Trust, London, UK.
Movember Foundation’s Global Action Plan Prostate Cancer Active Surveillance (GAP3) Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCurrently, follow-up protocols are applied equally to men on active surveillance (AS) for prostate cancer (PCa) regardless of findings at their initial follow-up biopsy. To determine whether less intensive follow-up is suitable following negative biopsy findings, we assessed the risk of converting to active treatment, any subsequent upgrading, volume progression (>33% positive cores), and serious upgrading (grade group >2) for negative compared with positive findings on initial follow-up biopsy.

methods13,161 men from 24 centres participating in the Global Action Plan Active Surveillance Prostate Cancer [GAP3] consortium database, with baseline grade group ≤2, PSA ≤ 20 ng/mL, cT-stage 1-2, diagnosed after 1995, and ≥1 follow-up biopsy, were included in this study. Risk of converting to treatment was assessed using multivariable mixed-effects survival regression. Odds of volume progression, any upgrading and serious upgrading were assessed using mix-effects binary logistic regression for men with ≥2 surveillance biopsies.

results27% of the cohort (n = 3590) had no evidence of PCa at their initial biopsy. Over 50% of subsequent biopsies in this group were also negative. A negative initial biopsy was associated with lower risk of conversion (adjusted hazard ratio: 0.45; 95% confidence interval [CI]: 0.42-0.49), subsequent upgrading (adjusted odds ratio [OR]: 0.52; 95%CI: 0.45-0.62) and serious upgrading (OR: 0.74; 95%CI: 0.59-92). Radiological progression was not assessed due to limited imaging data.

conclusionDespite heterogeneity in follow-up schedules, findings from this global study indicated reduced risk of converting to treatment, volume progression, any upgrading and serious upgrading among men whose initial biopsy findings were negative compared with positive. Given the low risk of progression and high likelihood of further negative biopsy findings, consideration should be given to decreasing follow-up intensity for this group to reduce unnecessary invasive biopsies.

Indexed as

Prostatic NeoplasmsBiopsyHumansLogistic ModelsMaleNeoplasm GradingProstate-Specific AntigenWatchful WaitingProstate-Specific Antigen

Identifiers

PMID36008540
PMCPMC10247354

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.