Evidence map›Paper›PMID 32594208›Full record

ArticleEuropean radiology2020

Clinically significant prostate cancer detection and segmentation in low-risk patients using a convolutional neural network on multi-parametric MRI.

Muhammad Arif, Ivo G Schoots, Jose Castillo Tovar, Chris H Bangma, Gabriel P Krestin, Monique J Roobol, Wiro Niessen, Jifke F Veenland

Open access · hybridAbstract read
In one paragraph

Article in European radiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

55 citing papers in PubMed, 113 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

8 authors at 1 institution in 1 country.

Muhammad ArifDepartment of Radiology & Nuclear Medicine, Erasmus University Medical Center, Wytemaweg 80, Room Na 2512 Erasmus MC, 3015 CN, Rotterdam, The Netherlands. a.muhammad@erasmusmc.nl.ORCID http://orcid.org/0000-0002-5141-0881
Ivo G SchootsDepartment of Radiology & Nuclear Medicine, Erasmus University Medical Center, Wytemaweg 80, Room Na 2512 Erasmus MC, 3015 CN, Rotterdam, The Netherlands.
Jose Castillo TovarDepartment of Radiology & Nuclear Medicine, Erasmus University Medical Center, Wytemaweg 80, Room Na 2512 Erasmus MC, 3015 CN, Rotterdam, The Netherlands.
Chris H BangmaDepartment of Urology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Gabriel P KrestinDepartment of Radiology & Nuclear Medicine, Erasmus University Medical Center, Wytemaweg 80, Room Na 2512 Erasmus MC, 3015 CN, Rotterdam, The Netherlands.
Monique J RoobolDepartment of Urology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Wiro NiessenDepartment of Radiology & Nuclear Medicine, Erasmus University Medical Center, Wytemaweg 80, Room Na 2512 Erasmus MC, 3015 CN, Rotterdam, The Netherlands.
Jifke F VeenlandDepartment of Radiology & Nuclear Medicine, Erasmus University Medical Center, Wytemaweg 80, Room Na 2512 Erasmus MC, 3015 CN, Rotterdam, The Netherlands.
Erasmus MC · NL

Funding

NWO-TTW 15173
6 · The paper itself

Abstract

objectivesTo develop an automatic method for identification and segmentation of clinically significant prostate cancer in low-risk patients and to evaluate the performance in a routine clinical setting.

methodsA consecutive cohort (n = 292) from a prospective database of low-risk patients eligible for the active surveillance was selected. A 3-T multi-parametric MRI at 3 months after inclusion was performed. Histopathology from biopsies was used as reference standard. MRI positivity was defined as PI-RADS score ≥ 3, histopathology positivity was defined as ISUP grade ≥ 2. The selected cohort contained four patient groups: (1) MRI-positive targeted biopsy-positive (n = 116), (2) MRI-negative systematic biopsy-negative (n = 55), (3) MRI-positive targeted biopsy-negative (n = 113), (4) MRI-negative systematic biopsy-positive (n = 8). Group 1 was further divided into three sets and a 3D convolutional neural network was trained using different combinations of these sets. Two MRI sequences (T2w, b = 800 DWI) and the ADC map were used as separate input channels for the model. After training, the model was evaluated on the remaining group 1 patients together with the patients of groups 2 and 3 to identify and segment clinically significant prostate cancer.

resultsThe average sensitivity achieved was 82-92% at an average specificity of 43-76% with an area under the curve (AUC) of 0.65 to 0.89 for different lesion volumes ranging from > 0.03 to > 0.5 cc.

conclusionsThe proposed deep learning computer-aided method yields promising results in identification and segmentation of clinically significant prostate cancer and in confirming low-risk cancer (ISUP grade ≤ 1) in patients on active surveillance. KEY POINTS: • Clinically significant prostate cancer identification and segmentation on multi-parametric MRI is feasible in low-risk patients using a deep neural network. • The deep neural network for significant prostate cancer localization performs better for lesions with larger volumes sizes (> 0.5 cc) as compared to small lesions (> 0.03 cc). • For the evaluation of automatic prostate cancer segmentation methods in the active surveillance cohort, the large discordance group (MRI positive, targeted biopsy negative) should be included.

Indexed as

Multiparametric Magnetic Resonance ImagingPattern Recognition, AutomatedAgedAlgorithmsArea Under CurveBiopsyCohort StudiesDeep LearningHumansImage Processing, Computer-AssistedMaleMiddle AgedNeural Networks, ComputerProstateProstatic NeoplasmsReproducibility of ResultsActive surveillanceDiagnosis, computer-assistedMulti-parametric magnetic resonance imagingNeural networks (computer)Prostate cancer

Identifiers

PMID32594208
PMCPMC7599141
OpenAlexW3037553776

What OpenQuestion holds

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LicenceCC BY
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.