Evidence map›Paper›PMID 37582946›Full record

ArticleNPJ precision oncology2023

An international multi-institutional validation study of the algorithm for prostate cancer detection and Gleason grading.

Yuri Tolkach, Vlado Ovtcharov, Alexey Pryalukhin, Marie-Lisa Eich, Nadine Therese Gaisa, Martin Braun, Abdukhamid Radzhabov, Alexander Quaas, Peter Hammerer, Ansgar Dellmann and 12 more

Open access · goldAbstract read
In one paragraph

Article in NPJ precision oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 25 citations in OpenAlex.

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  15. Artificial intelligence in prostate cancer.Chinese medical journal · 2025
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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

22 authors at 12 institutions in 8 countries.

Yuri Tolkach *Institute of Pathology, University Hospital Cologne, Cologne, Germany. yuri.tolkach@gmail.com.ORCID http://orcid.org/0000-0001-5239-2841
Vlado Ovtcharov *Indica Labs, Albuquerque, NM, USA.
Alexey Pryalukhin *Institute of Pathology, Landesklinikum Wiener Neustadt, Wiener Neustadt, Austria.
Marie-Lisa EichInstitute of Pathology, University Hospital Cologne, Cologne, Germany.
Nadine Therese GaisaInstitute of Pathology, University Hospital Aachen, Aachen, Germany.
Martin BraunInstitute of Pathology Troisdorf, Troisdorf, Germany.
Abdukhamid RadzhabovUrology Clinic, Municipal Clinic of Brunswick, Brunswick, Germany.ORCID http://orcid.org/0000-0003-1948-5792
Alexander QuaasInstitute of Pathology, University Hospital Cologne, Cologne, Germany.
Peter HammererUrology Clinic, Municipal Clinic of Brunswick, Brunswick, Germany.
Ansgar DellmannInstitute of Pathology, Municipal Clinic of Brunswick, Brunswick, Germany.
Wolfgang HullaInstitute of Pathology, Landesklinikum Wiener Neustadt, Wiener Neustadt, Austria.
Michael C HaffnerDivisions of Human Biology and Clinical Research, Fred Hutch Cancer Center, Seattle, WA, USA.
Henning ReisDr. Senckenberg Institute of Pathology, University Hospital Frankfurt, Goethe University Frankfurt, Frankfurt am Main, Germany.
Ibrahim FahoumDepartment of Pathology, Sourasky Medical Center, Tel Aviv, Israel.
Iryna SamarskaDepartment of Pathology, University Hospital Maastricht, Maastricht, The Netherlands.ORCID http://orcid.org/0000-0003-4092-0672
Artem BorbatDepartment of Pathology, Burnasyan Federal Medical Biophysical Center of Federal Medical Biological Agency, Moscow, Russia.ORCID http://orcid.org/0000-0002-9699-8375
Hoa PhamDepartment of Pathology, Bach Mai Hospital, Hanoi, Vietnam.
Axel HeidenreichClinic of Urology, University Hospital Cologne, Cologne, Germany.
Sebastian KleinInstitute of Pathology, University Hospital Cologne, Cologne, Germany.ORCID http://orcid.org/0000-0002-2188-9377
George NettoDepartment of Pathology, University of Alabama, Birmingham, AL, USA.
Peter CaieIndica Labs, Albuquerque, NM, USA.
Reinhard BuettnerInstitute of Pathology, University Hospital Cologne, Cologne, Germany.ORCID http://orcid.org/0000-0001-8806-4786
University Hospital Cologne · DEFachhochschule Wiener Neustadt · ATSandia National Laboratories California · USAtos Medical · DEFederal Medical-Biological Agency · RUFred Hutch Cancer Center · USGoethe University Frankfurt · DEMaastricht University Medical Centre · NLTel Aviv Sourasky Medical Center · ILUniversitätsklinikum Aachen · DEUniversity of Alabama at Birmingham · USUniversity of Nagasaki · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathologic examination of prostate biopsies is time consuming due to the large number of slides per case. In this retrospective study, we validate a deep learning-based classifier for prostate cancer (PCA) detection and Gleason grading (AI tool) in biopsy samples. Five external cohorts of patients with multifocal prostate biopsy were analyzed from high-volume pathology institutes. A total of 5922 H&E sections representing 7473 biopsy cores from 423 patient cases (digitized using three scanners) were assessed concerning tumor detection. Two tumor-bearing datasets (core n = 227 and 159) were graded by an international group of pathologists including expert urologic pathologists (n = 11) to validate the Gleason grading classifier. The sensitivity, specificity, and NPV for the detection of tumor-bearing biopsies was in a range of 0.971-1.000, 0.875-0.976, and 0.988-1.000, respectively, across the different test cohorts. In several biopsy slides tumor tissue was correctly detected by the AI tool that was initially missed by pathologists. Most false positive misclassifications represented lesions suspicious for carcinoma or cancer mimickers. The quadratically weighted kappa levels for Gleason grading agreement for single pathologists was 0.62-0.80 (0.77 for AI tool) and 0.64-0.76 (0.72 for AI tool) for the two grading datasets, respectively. In cases where consensus for grading was reached among pathologists, kappa levels for AI tool were 0.903 and 0.855. The PCA detection classifier showed high accuracy for PCA detection in biopsy cases during external validation, independent of the institute and scanner used. High levels of agreement for Gleason grading were indistinguishable between experienced genitourinary pathologists and the AI tool.

Identifiers

PMID37582946
PMCPMC10427608
OpenAlexW4385835592

What OpenQuestion holds

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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.