Evidence map›Paper›PMID 28583312›Full record

ArticleEuropean urology2017

Prognostic Impact of a 12-gene Progression Score in Non-muscle-invasive Bladder Cancer: A Prospective Multicentre Validation Study.

Lars Dyrskjøt, Thomas Reinert, Ferran Algaba, Emil Christensen, Daan Nieboer, Gregers G Hermann, Karin Mogensen, Willemien Beukers, Mirari Marquez, Ulrika Segersten and 23 more

Abstract readMulticenter StudyValidation Study
PubMed Publisher
In one paragraph

Article in European urology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing 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

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

52 citing papers in PubMed.

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  12. Bladder cancer.Nature reviews. Disease primers · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

33 authors.

Lars DyrskjøtDepartment of Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark. Electronic address: lars@clin.au.dk.
Thomas ReinertDepartment of Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark.
Ferran AlgabaSection of Pathology, Fundació Puigvert, University Autonoma de Barcelona, Barcelona, Spain.
Emil ChristensenDepartment of Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark.
Daan NieboerDepartment of Public Health, Erasmus MC, Rotterdam, The Netherlands.
Gregers G HermannDepartment of Urology, Frederiksberg Hospital, Frederiksberg, Denmark.
Karin MogensenDepartment of Urology, Frederiksberg Hospital, Frederiksberg, Denmark.
Willemien BeukersDepartment of Pathology, Erasmus MC, Rotterdam, The Netherlands.
Mirari MarquezSpanish National Cancer Research Centre, Madrid, Spain.
Ulrika SegerstenDepartment of Surgical Sciences, Uppsala University, Uppsala, Sweden.
Søren HøyerDepartment of Pathology, Aarhus University Hospital, Aarhus, Denmark.
Benedicte P UlhøiDepartment of Pathology, Aarhus University Hospital, Aarhus, Denmark.
Arndt HartmannInstitute of Pathology, University Hospital Erlangen, Friedrich Alexander-University Erlangen-Nürnberg, Erlangen, Germany.
Robert StöhrInstitute of Pathology, University Hospital Erlangen, Friedrich Alexander-University Erlangen-Nürnberg, Erlangen, Germany.
Sven WachDepartment of Urology, University Hospital Erlangen, Friedrich Alexander-University Erlangen-Nürnberg, Erlangen, Germany.
Roman NawrothDepartment of Urology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Kristina SchwambornInstitute of Pathology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Cane TulicClinic of Urology, Clinical Centre of Serbia, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
Tatjana SimicInstitute of Medical and Clinical Biochemistry, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
Kerstin JunkerDepartment of Urology, Saarland University, Homburg, Germany.
Niels HarvingDepartment of Urology, Aalborg University Hospital, Aalborg, Denmark.
Astrid C PetersenDepartment of Pathology, Aalborg University Hospital, Aalborg, Denmark.
Jørgen B JensenDepartment of Urology, Aarhus University Hospital, Aarhus, Denmark.
Bastian KeckDepartment of Urology, University Hospital Erlangen, Friedrich Alexander-University Erlangen-Nürnberg, Erlangen, Germany.
Marc-Oliver GrimmDepartment of Urology, Friedrich-Schiller-University Jena, Jena, Germany.
Marcus HorstmannDepartment of Urology, Friedrich-Schiller-University Jena, Jena, Germany.
Tobias MaurerDepartment of Urology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Ewout W SteyerbergDepartment of Public Health, Erasmus MC, Rotterdam, The Netherlands.
Ellen C ZwarthoffDepartment of Pathology, Erasmus MC, Rotterdam, The Netherlands.
Francisco X RealSpanish National Cancer Research Centre, Madrid, Spain; Departament de Ciències Experimentals i de la Salut, Universitat Pompeu Fabra, Barcelona, Spain.
Núria MalatsSpanish National Cancer Research Centre, Madrid, Spain.
Per-Uno MalmströmDepartment of Surgical Sciences, Uppsala University, Uppsala, Sweden.
Torben F ØrntoftDepartment of Molecular Medicine, Aarhus University Hospital, Aarhus, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProgression of non-muscle-invasive bladder cancer (NMIBC) to muscle-invasive bladder cancer (MIBC) is life-threatening and cannot be accurately predicted using clinical and pathological risk factors. Biomarkers for stratifying patients to treatment and surveillance are greatly needed.

objectiveTo validate a previously developed 12-gene progression score to predict progression to MIBC in a large, multicentre, prospective study. DESIGN, SETTING, AND

participantsWe enrolled 1224 patients in ten European centres between 2008 and 2012. A total of 750 patients (851 tumours) fulfilled the inclusion and sample quality criteria for testing. Patients were followed for an average of 28 mo (range 0-76). A 12-gene real-time qualitative polymerase chain reaction assay was performed for all tumours and progression scores were calculated using a predefined formula and cut-off values. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: We measured progression to MIBC using Cox regression analysis and log-rank tests for comparing survival distributions. RESULTS AND LIMITATIONS: The progression score was significantly (p<0.001) associated with age, stage, grade, carcinoma in situ, bacillus Calmette-Guérin treatment, European Organisation for Research and Treatment of Cancer risk score, and disease progression. Univariate Cox regression analysis showed that patients molecularly classified as high risk experienced more frequent disease progression (hazard ratio 5.08, 95% confidence interval 2.2-11.6; p<0.001). Multivariable Cox regression models showed that the progression score added independent prognostic information beyond clinical and histopathological risk factors (p<0.001), with an increase in concordance statistic from 0.82 to 0.86. The progression score showed high correlation (R

conclusionsThe 12-gene progression score had independent prognostic power beyond clinical and histopathological risk factors, and may help in stratifying NMIBC patients to optimise treatment and follow-up regimens. PATIENT SUMMARY: Clinical use of a 12-gene molecular test for disease aggressiveness may help in stratifying patients with non-muscle-invasive bladder cancer to optimal treatment regimens.

Indexed as

Real-Time Polymerase Chain ReactionAgedArea Under CurveBiomarkers, TumorDisease ProgressionFemaleGenetic Predisposition to DiseaseHumansKaplan-Meier EstimateMaleMultivariate AnalysisNeoplasm InvasivenessPhenotypePredictive Value of TestsProportional Hazards ModelsProspective StudiesBiomarkers, TumorBladder cancerNon–muscle-invasive bladder cancerPrognostic biomarkerProgression riskProspective studyReal-time qualitative polymerase chain reactionValidation

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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.