Evidence map›Paper›PMID 25991476›Full record

ArticleEuropean radiology2015

Haralick texture analysis of prostate MRI: utility for differentiating non-cancerous prostate from prostate cancer and differentiating prostate cancers with different Gleason scores.

Andreas Wibmer, Hedvig Hricak, Tatsuo Gondo, Kazuhiro Matsumoto, Harini Veeraraghavan, Duc Fehr, Junting Zheng, Debra Goldman, Chaya Moskowitz, Samson W Fine and 4 more

Abstract read
In one paragraph

Article in European radiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 199 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
199citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

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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

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3 · Its place in the literature

Who cites it

199 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  14. Quantitative Prostate MRI, From theAJR. American journal of roentgenology · 2025
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139 more citing papers are in PubMed but not listed here.

4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Andreas WibmerDepartment of Radiology, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, 10065, New York City, NY, USA, a.wibmer@gmx.net.
Hedvig Hricak
Tatsuo Gondo
Kazuhiro Matsumoto
Harini Veeraraghavan
Duc Fehr
Junting Zheng
Debra Goldman
Chaya Moskowitz
Samson W Fine
Victor E Reuter
James Eastham
Evis Sala
Hebert Alberto Vargas

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

objectivesTo investigate Haralick texture analysis of prostate MRI for cancer detection and differentiating Gleason scores (GS).

methodsOne hundred and forty-seven patients underwent T2- weighted (T2WI) and diffusion-weighted prostate MRI. Cancers ≥0.5 ml and non-cancerous peripheral (PZ) and transition (TZ) zone tissue were identified on T2WI and apparent diffusion coefficient (ADC) maps, using whole-mount pathology as reference. Texture features (Energy, Entropy, Correlation, Homogeneity, Inertia) were extracted and analysed using generalized estimating equations.

resultsPZ cancers (n = 143) showed higher Entropy and Inertia and lower Energy, Correlation and Homogeneity compared to non-cancerous tissue on T2WI and ADC maps (p-values: <.0001-0.008). In TZ cancers (n = 43) we observed significant differences for all five texture features on the ADC map (all p-values: <.0001) and for Correlation (p = 0.041) and Inertia (p = 0.001) on T2WI. On ADC maps, GS was associated with higher Entropy (GS 6 vs. 7: p = 0.0225; 6 vs. >7: p = 0.0069) and lower Energy (GS 6 vs. 7: p = 0.0116, 6 vs. >7: p = 0.0039). ADC map Energy (p = 0.0102) and Entropy (p = 0.0019) were significantly different in GS ≤3 + 4 versus ≥4 + 3 cancers; ADC map Entropy remained significant after controlling for the median ADC (p = 0.0291).

conclusionSeveral Haralick-based texture features appear useful for prostate cancer detection and GS assessment. KEY POINTS: • Several Haralick texture features may differentiate non-cancerous and cancerous prostate tissue. • Tumour Energy and Entropy on ADC maps correlate with Gleason score. • T2w-image-derived texture features are not associated with the Gleason score.

Indexed as

AdultAgedDiagnosis, DifferentialDiffusion Magnetic Resonance ImagingHumansImage Processing, Computer-AssistedMaleMiddle AgedNeoplasm GradingProstatectomyProstatic NeoplasmsRetrospective StudiesTumor Burden

Identifiers

PMID25991476
PMCPMC5026307

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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.