Evidence map›Paper›PMID 38627253›Full record

ArticleThe British journal of radiology2024

Accuracy of MRI-ultrasound fusion-guided and systematic biopsy of the prostate.

Thomas In de Braekt, Sanne B T van Rooij, Alette W Daniels-Gooszen, Wout A Scheepens, Rik de Jongh, Steven L Bosch, Joost Nederend

Open access · bronzeAbstract read
In one paragraph

Article in The British journal of radiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

4 citing papers in PubMed, 6 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

7 authors at 3 institutions in 2 countries.

Thomas In de BraektDepartment of Radiology, Catharina Hospital, Eindhoven, 5623 EJ, The Netherlands.ORCID 0000-0001-7945-3421
Sanne B T van RooijDepartment of Radiology, Antwerp University Hospital, Edegem, 2650, Belgium.
Alette W Daniels-GooszenDepartment of Radiology, Catharina Hospital, Eindhoven, 5623 EJ, The Netherlands.
Wout A ScheepensDepartment of Urology, Catharina Hospital, Eindhoven, 5623 EJ, The Netherlands.
Rik de JonghDepartment of Urology, Catharina Hospital, Eindhoven, 5623 EJ, The Netherlands.
Steven L BoschDepartment of Pathology, Eurofins-PAMM, Eindhoven, 5623 EJ, The Netherlands.
Joost NederendDepartment of Radiology, Catharina Hospital, Eindhoven, 5623 EJ, The Netherlands.
Radboud University Nijmegen · NLAntwerp University Hospital · BEEurofins (Netherlands) · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesProstate multiparametric MRI (mpMRI) with subsequent targeted biopsy of suspicious lesions has a critical role in the diagnostic workup of prostate cancer. The objective was to evaluate the diagnostic accuracy of systematic biopsies, targeted biopsies, and the combination of both in prostate cancer detection.

methodsFrom January 1, 2013 to June 1, 2022, biopsy-naïve and prior biopsy-negative patients who underwent both systematic and targeted biopsies were included. MRIs were evaluated according to PI-RADS with biopsy threshold set at PI-RADS ≥3. Systematic biopsies consisted of 8-12 cores, based on prostate volume. Overall prostate cancer and clinically significant cancer (Gleason Score ≥3 + 4) detection rates were stratified based on PI-RADS and location within the prostate, and compared between biopsy types using McNemar test.

resultsAmong 867 patients, 615 had prostate cancer, with 434 clinically significant cases. Overall detection rates were: PI-RADS 3 48%, PI-RADS 4 72%, and PI-RADS 5 90%. Detection rates for clinically significant cancer were 21%, 53%, and 72%, respectively. The combination of biopsy methods was most accurate in detecting clinically significant prostate cancer (P < .001). Targeted biopsies alone detected more clinically significant prostate cancer than systematic biopsies alone (43.1% vs 40.3%, P = .046). For posterior PI-RADS 5 lesions, no statistically significant difference was found between all biopsy methods.

conclusionsIn the detection of clinically significant prostate cancer, the combination of systematic and targeted biopsies proves most effective. Targeted biopsies rarely missed significant cancer for posterior PI-RADS 5 lesions, suggesting systematic biopsies could be reserved for instances where targeted biopsy results are negative. ADVANCES IN KNOWLEDGE: This study emphasizes on the efficacy of mpMRI and targeted biopsies in suspected prostate cancer in real-world clinical context. For PI-RADS 5 lesions, systematic biopsies provide limited clinical benefit and may only be necessary when targeted biopsy results are negative.

Indexed as

Image-Guided BiopsyProstateProstatic NeoplasmsUltrasonography, InterventionalAgedHumansMagnetic Resonance ImagingMagnetic Resonance Imaging, InterventionalMaleMiddle AgedMultimodal ImagingMultiparametric Magnetic Resonance ImagingRetrospective Studiesbiopsy-naïveMRI-ultrasound fusion biopsyPI-RADSprior biopsy negativeprostate cancersystematic biopsytargeted biopsy

Identifiers

PMID38627253
PMCPMC11135791
OpenAlexW4394874339

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.