Evidence map›Paper›PMID 38001723›Full record

ArticleCancers2023

Quantification of Gleason Pattern 4 at MRI-Guided Biopsy to Predict Adverse Pathology at Radical Prostatectomy in Intermediate-Risk Prostate Cancer Patients.

Hubert Kamecki, Łukasz Mielczarek, Stanisław Szempliński, Małgorzata Dębowska, Paweł Rajwa, Michael Baboudjian, Jakob Klemm, Juan Gómez Rivas, Elza Modzelewska, Omar Tayara and 6 more

Abstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Trial
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

16 authors.

Hubert KameckiSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.ORCID 0000-0001-8387-1474
Łukasz MielczarekSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Stanisław SzemplińskiSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Małgorzata DębowskaNałęcz Institute of Biocybernetics and Biomedical Engineering, Polish Academy of Sciences, 02-109 Warsaw, Poland.
Paweł RajwaDepartment of Urology, Comprehensive Cancer Center, Medical University of Vienna, 1090 Vienna, Austria.
Michael BaboudjianDepartment of Urology, North Hospital, AP-HM, 13007 Marseilles, France.ORCID 0000-0001-6935-3873
Jakob KlemmDepartment of Urology, Comprehensive Cancer Center, Medical University of Vienna, 1090 Vienna, Austria.
Juan Gómez RivasDepartment of Urology, Hospital Clinico San Carlos, 28040 Madrid, Spain.
Elza ModzelewskaSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Omar TayaraSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Wojciech MalewskiSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Przemysław SzostekSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Sławomir PoletajewSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.ORCID 0000-0001-7664-9816
Piotr KrystSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.ORCID 0000-0003-2551-0296
Roman SosnowskiDepartment of Urology and Oncological Urology, Warmian-Masurian Cancer Center, 10-228 Olsztyn, Poland.ORCID 0000-0002-4894-4233
Łukasz NykSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundData on Gleason pattern 4 (GP4) amount in biopsy tissue is important for prostate cancer (PC) risk assessment. We aim to investigate which GP4 quantification method predicts adverse pathology (AP) at radical prostatectomy (RP) the best in men diagnosed with intermediate-risk (IR) PC at magnetic resonance imaging (MRI)-guided biopsy.

methodsWe retrospectively included 123 patients diagnosed with IR PC (prostate-specific antigen <20 ng/mL, grade group (GG) 2 or 3, no iT3 on MRI) at MRI-guided biopsy, who underwent RP. Twelve GP4 amount-related parameters were developed, based on GP4 quantification method (absolute, relative to core, or cancer length) and site (overall, targeted, systematic biopsy, or worst specimen). Additionally, we calculated PV×GP4 (prostate volume × GP4 relative to core length in overall biopsy), aiming to represent the total GP4 volume in the prostate. The associations of GP4 with AP (GG ≥ 4, ≥pT3a, or pN1) were investigated.

resultsAP was reported in 39 (31.7%) of patients. GP4 relative to cancer length was not associated with AP. Of the 12 parameters, the highest ROC AUC value was seen for GP4 relative to core length in overall biopsy (0.65). an even higher AUC value was noted for PV × GP4 (0.67), with a negative predictive value of 82.8% at the optimal threshold.

conclusionsThe lack of an association of GP4 relative to cancer length with AP, contrasted with the better performance of other parameters, indicates directions for future research on PC risk stratification to accurately identify patients who may not require immediate treatment. Incorporating formulas aimed at GP4 volume assessment may lead to obtaining models with the best discrimination ability.

Indexed as

Gleason pattern 4prostate biopsyprostate cancerrisk stratification

Identifiers

PMID38001723
PMCPMC10670701

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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.