Evidence map›Paper›PMID 32645056›Full record

ArticlePloS one2020

Prostate MRI added to CAPRA, MSKCC and Partin cancer nomograms significantly enhances the prediction of adverse findings and biochemical recurrence after radical prostatectomy.

Kevin Sandeman, Juho T Eineluoto, Joona Pohjonen, Andrew Erickson, Tuomas P Kilpeläinen, Petrus Järvinen, Henrikki Santti, Anssi Petas, Mika Matikainen, Suvi Marjasuo and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 17% of its field
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

12 citing papers in PubMed, 16 citations in OpenAlex.

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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

13 authors at 1 institution in 1 country.

Kevin SandemanDepartment of Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Juho T EineluotoResearch Program in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.ORCID 0000-0003-1109-2994
Joona PohjonenResearch Program in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Andrew EricksonResearch Program in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Tuomas P KilpeläinenDepartment of Urology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Petrus JärvinenDepartment of Urology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Henrikki SanttiDepartment of Urology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Anssi PetasDepartment of Urology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Mika MatikainenDepartment of Urology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Suvi MarjasuoDepartment of Diagnostic Radiology, Medical Imaging Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Anu KenttämiesDepartment of Diagnostic Radiology, Medical Imaging Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Tuomas MirttiDepartment of Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Antti RannikkoResearch Program in Systems Oncology, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
University of Helsinki · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo determine the added value of preoperative prostate multiparametric MRI (mpMRI) supplementary to clinical variables and their role in predicting post prostatectomy adverse findings and biochemically recurrent cancer (BCR).

methodsAll consecutive patients treated at HUS Helsinki University Hospital with robot assisted radical prostatectomy (RALP) between 2014 and 2015 were included in the analysis. The mpMRI data, clinical variables, histopathological characteristics, and follow-up information were collected. Study end-points were adverse RALP findings: extraprostatic extension, seminal vesicle invasion, lymph node involvement, and BCR. The Memorial Sloan Kettering Cancer Center (MSKCC) nomogram, Cancer of the Prostate Risk Assessment (CAPRA) score and the Partin score were combined with any adverse findings at mpMRI. Predictive accuracy for adverse RALP findings by the regression models was estimated before and after the addition of MRI results. Logistic regression, area under curve (AUC), decision curve analyses, Kaplan-Meier survival curves and Cox proportional hazard models were used.

resultsPreoperative mpMRI data from 387 patients were available for analysis. Clinical variables alone, MSKCC nomogram or Partin tables were outperformed by models with mpMRI for the prediction of any adverse finding at RP. AUC for clinical parameters versus clinical parameters and mpMRI variables were 0.77 versus 0.82 for any adverse finding. For MSKCC nomogram versus MSKCC nomogram and mpMRI variables the AUCs were 0.71 and 0.78 for any adverse finding. For Partin tables versus Partin tables and mpMRI variables the AUCs were 0.62 and 0.73 for any adverse finding. In survival analysis, mpMRI-projected adverse RP findings stratify CAPRA and MSKCC high-risk patients into groups with distinct probability for BCR.

conclusionsPreoperative mpMRI improves the predictive value of commonly used clinical variables for pathological stage at RP and time to BCR. mpMRI is available for risk stratification prebiopsy, and should be considered as additional source of information to the standard predictive nomograms.

Indexed as

AgedHumansMagnetic Resonance ImagingMaleMiddle AgedNeoplasm Recurrence, LocalNomogramsPreoperative CarePrognosisProstateProstatectomyProstatic NeoplasmsRisk Assessment

Identifiers

PMID32645056
PMCPMC7347171
OpenAlexW3040961929

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.