Evidence map›Paper›PMID 31603818›Full record

ArticleIEEE transactions on medical imaging2020

Development and Assessment of a New Global Mammographic Image Feature Analysis Scheme to Predict Likelihood of Malignant Cases.

Morteza Heidari, Seyedehnafiseh Mirniaharikandehei, Wei Liu, Alan B Hollingsworth, Hong Liu, Bin Zheng

Abstract read
In one paragraph

Article in IEEE transactions on medical imaging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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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

6 authors.

Morteza Heidari
Seyedehnafiseh Mirniaharikandehei
Wei Liu
Alan B Hollingsworth
Hong Liu
Bin Zheng

Funding

Increasing Cancer Detection Yield Using Breast MRI Screening ModalityR01CA197150 · NCI · UNIVERSITY OF OKLAHOMA · PI HOLLINGSWORTH, ALAN B., LIU, HONG · 2015 to 2019
$2.5M
NCI NIH HHS R01 CA197150
6 · The paper itself

Abstract

This study aims to develop and evaluate a new computer-aided diagnosis (CADx) scheme based on analysis of global mammographic image features to predict likelihood of cases being malignant. An image dataset involving 1,959 cases was retrospectively assembled. Suspicious lesions were detected and biopsied in each case. Among them, 737 cases are malignant and 1,222 are benign. Each case includes four mammograms of craniocaudal and mediolateral oblique view of left and right breasts. CADx scheme is applied to pre-process mammograms, generate two image maps in frequency domain using discrete cosine transform and fast Fourier transform, compute bilateral image feature differences from left and right breasts, and apply a support vector machine (SVM) to predict likelihood of the case being malignant. Three sub-groups of image features were computed from the original mammograms and two transformation maps. Four SVMs using three sub-groups of image features and fusion of all features were trained and tested using a 10-fold cross-validation method. The computed areas under receiver operating characteristic curves (AUCs) range from 0.85 to 0.91 using image features computed from one of three sub-groups, respectively. By fusion of all image features computed in three sub-groups, the fourth SVM yields a significantly higher performance with AUC = 0.96±0.01 (p<0.01). This study demonstrates feasibility of developing a new global image feature analysis based CADx scheme of mammograms with high performance. By avoiding difficulty and possible errors in breast lesion segmentation, this new CADx approach is more efficient in development and potentially more robust in future application.

Indexed as

AdultAgedAged, 80 and overBreastBreast NeoplasmsFemaleHumansMammographyMiddle AgedRadiographic Image Interpretation, Computer-AssistedROC CurveSupport Vector Machine

Identifiers

PMID31603818
PMCPMC7136147

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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.