Evidence map›Paper›PMID 33850745›Full record

ArticleTranslational andrology and urology2021

A first step towards a global nomogram to predict disease progression for men on active surveillance.

Mieke Van Hemelrijck, Xinge Ji, Jozien Helleman, Monique J Roobol, Daan Nieboer, Chris Bangma, Mark Frydenberg, Antti Rannikko, Lui Shiong Lee, Vincent Gnanapragasam and 2 more

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Article in Translational andrology and urology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 42% of its field
1 · What the graph read from it

What it found

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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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 7 institutions in 6 countries.

Mieke Van HemelrijckTranslational Oncology & Urology Research (TOUR), School of Cancer and Pharmaceutical Sciences, King's College London, London, UK.
Xinge JiDepartment of Quantitative Health Sciences, Cleveland Clinic, Cleveland, OH, USA.
Jozien HellemanDepartment of Urology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Monique J RoobolDepartment of Urology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Daan NieboerDepartment of Urology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Chris BangmaDepartment of Urology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Mark FrydenbergCabrini Institute, Malvern, Australia.
Antti RannikkoDepartment of Urology, Helsinki University and Helsinki University Hospital, Helsinki, Finland.
Lui Shiong LeeDepartment of Urology, Sengkang General Hospital and Singapore General Hospital, Singapore, Singapore.
Vincent GnanapragasamAcademic Urology Group, Department of Surgery and Oncology, University of Cambridge, Cambridge, UK.
Michael W KattanDepartment of Quantitative Health Sciences, Cleveland Clinic, Cleveland, OH, USA.
Movember Foundation’s Global Action Plan Prostate Cancer Active Surveillance (GAP3) Consortium
Erasmus MC · NLCleveland Clinic · USCabrini Hospital · AUKing's College London · GBSingapore General Hospital · SGUniversity of Cambridge · GBUniversity of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSigns of disease progression (28%) and conversion to active treatment without evidence of disease progression (13%) are the main reasons for discontinuation of active surveillance (AS) in men with localised prostate cancer (PCa). We aimed to develop a nomogram to predict disease progression in these patients.

methodsAs a first step in the development of a nomogram, using data from Movembers' GAP3 Consortium (n=14,380), we assessed heterogeneity between centres in terms of risk of disease progression. We started with assessment of baseline hazards for disease progression based on grouping of centres according to follow-up protocols [high: yearly; intermediate: ~2 yearly; and low: at year 1, 4 & 7 (i.e., PRIAS)]. We conducted cause-specific random effect Cox proportional hazards regression to estimate risk of disease progression by centre in each group.

resultsDisease progression rates varied substantially between centres [median hazard ratio (MHR): 2.5]. After adjustment for various clinical factors (age, year of diagnosis, Gleason grade group, number of positive cores and PSA), substantial heterogeneity in disease progression remained between centres.

conclusionsWhen combining worldwide data on AS, we noted unexplained differences of disease progression rate even after adjustment for various clinical factors. This suggests that when developing a global nomogram, local adjustments for differences in risk of disease progression and competing outcomes such as conversion to active treatment need to be considered.

Indexed as

active surveillance (AS)discontinuationnomogramProstate cancer (PCa)worldwide

Identifiers

PMID33850745
PMCPMC8039580
OpenAlexW3141598393

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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.