Evidence map›Paper›PMID 26013424›Full record

Trial reportJournal of cancer research and clinical oncology2015

The use of targeted MR-guided prostate biopsy reduces the risk of Gleason upgrading on radical prostatectomy.

Christian Arsov, Nikolaus Becker, Robert Rabenalt, Andreas Hiester, Michael Quentin, Frederic Dietzel, Gerald Antoch, Helmut E Gabbert, Peter Albers, Lars Schimmöller

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Journal of cancer research and clinical oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 60 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

10 authors at 2 institutions in 1 country.

Christian ArsovDepartment of Urology, Medical Faculty, Heinrich-Heine University, Moorenstr. 5, 40225, Düsseldorf, Germany. christian.arsov@med.uni-duesseldorf.de.
Nikolaus BeckerDivision of Cancer Epidemiology (C020), German Cancer Research Center Heidelberg, 69120, Heidelberg, Germany.
Robert RabenaltDepartment of Urology, Medical Faculty, Heinrich-Heine University, Moorenstr. 5, 40225, Düsseldorf, Germany.
Andreas HiesterDepartment of Urology, Medical Faculty, Heinrich-Heine University, Moorenstr. 5, 40225, Düsseldorf, Germany.
Michael QuentinDepartment of Diagnostic and Interventional Radiology, Medical Faculty, Heinrich-Heine University, 40225, Düsseldorf, Germany.
Frederic DietzelDepartment of Diagnostic and Interventional Radiology, Medical Faculty, Heinrich-Heine University, 40225, Düsseldorf, Germany.
Gerald AntochDepartment of Diagnostic and Interventional Radiology, Medical Faculty, Heinrich-Heine University, 40225, Düsseldorf, Germany.
Helmut E GabbertDepartment of Pathology, Medical Faculty, Heinrich-Heine University, 40225, Düsseldorf, Germany.
Peter AlbersDepartment of Urology, Medical Faculty, Heinrich-Heine University, Moorenstr. 5, 40225, Düsseldorf, Germany.
Lars SchimmöllerDepartment of Diagnostic and Interventional Radiology, Medical Faculty, Heinrich-Heine University, 40225, Düsseldorf, Germany.
Heinrich Heine University Düsseldorf · DEGerman Cancer Research Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeGleason grading is the strongest predictor of prostate cancer outcome and commonly used to decide for or against the different treatment options. However, Gleason upgrading between systematic transrectal ultrasound-guided prostate biopsy (TRUS-GB) and radical prostatectomy (RPE) has frequently been observed. With respect to the high accuracy of multiparametric MRI (mpMRI) for high-grade cancers and the higher percentage of cancer involvement per biopsy core in targeted MR-guided prostate biopsy (MR-GB), we hypothesized that MR-GB reduces the risk of Gleason upgrading on RPE as compared to the gold standard. The purpose of this study was to compare the rate of Gleason upgrading on RPE for MR-GB, TRUS-GB, and the combination of both biopsy modalities.

methodsOverall, 52 consecutive patients with RPE had received an mpMRI of the prostate and subsequently underwent targeted MR-GB prior to surgery. All patients underwent an additional TRUS-GB during the same biopsy session. Gleason grading was measured by two different methods: the conventional Gleason score (cGS = primary + secondary pattern) and the highest Gleason pattern (hGP).

resultsIn relation to TRUS-GB, MR-GB alone showed lower rates of upgrading when comparing the cGS (40.4 vs. 50.0 %) and the hGP (21.2 vs. 32.7 %). The combination of MR-GB and TRUS-GB showed the lowest rates of upgrading (cGS: 28.8 %; hGP: 11.5 %), and compared to TRUS-GB, significantly reduced the risk of upgrading for both measurements of Gleason grading (cGS: OR 0.41, 95 % CL 0.18-0.91, p = 0.0289; hGP: OR 0.27, 95 % CL 0.10-0.75, p = 0.0123).

conclusionMpMRI and targeted MR-GB are useful tools to better characterize and stage the extent of disease, and therefore enable the urologist to better risk-stratify and counsel the patient. The combined use of targeted MR-GB and TRUS-GB presents the least risk of Gleason underestimation.

Indexed as

AgedBiopsy, NeedleHumansMagnetic Resonance ImagingMaleMiddle AgedNeoplasm GradingProstateProstatectomyProstatic NeoplasmsRetrospective StudiesTreatment OutcomeGleason gradingGleason scoreImage-guided prostate biopsyMagnetic resonance imagingMR-guided prostate biopsyProstate cancer

Identifiers

PMID26013424
PMCPMC11823980
OpenAlexW396498207

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.