Evidence map›Paper›PMID 30697755›Full record

ArticleMedical physics2019

Derived mammographic masking measures based on simulated lesions predict the risk of interval cancer after controlling for known risk factors: a case-case analysis.

Benjamin Hinton, Lin Ma, Amir Pasha Mahmoudzadeh, Serghei Malkov, Bo Fan, Heather Greenwood, Bonnie Joe, Vivian Lee, Fredrik Strand, Karla Kerlikowske and 1 more

Abstract read
In one paragraph

Article in Medical physics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

11 authors.

Benjamin HintonDepartment of Bioengineering, UC-San Francisco & UC-Berkeley Joint Program, San Francisco, CA, 94143, USA.
Lin MaKaiser Permanente Division of Research, Oakland, CA, 94612, USA.
Amir Pasha MahmoudzadehDepartment of Radiology and Biomedical Imaging, UC-San Francisco, San Francisco, CA, 94143, USA.
Serghei MalkovApplied Materials, Santa Clara, CA, 95054, USA.
Bo FanDepartment of Bioengineering, UC-San Francisco & UC-Berkeley Joint Program, San Francisco, CA, 94143, USA.
Heather GreenwoodDepartment of Radiology and Biomedical Imaging, UC-San Francisco, San Francisco, CA, 94143, USA.
Bonnie JoeDepartment of Radiology and Biomedical Imaging, UC-San Francisco, San Francisco, CA, 94143, USA.
Vivian LeeResearch Advocate, UCSF Breast Science Advocacy Core, San Francisco, CA, 94143, USA.
Fredrik StrandDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Solna, Sweden.
Karla KerlikowskeDepartment of Epidemiology and Biostatistics, UCSF, San Francisco, CA, 94143, USA.
John ShepherdUniversity of Hawaii Cancer Center, Honolulu, HI, 96813, USA.

Funding

Risk-based Imaging Strategies to Improve Breast Cancer Surveillance OutcomesP01CA154292 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KARLA M KERLIKOWSKE · 2011 to 2026
$52.9M
Lesion Composition and Quantitative Imaging Analysis on Breast Cancer DiagnosisR01CA166945 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI GIGER, MARYELLEN L., SHEPHERD, JOHN ALAN · 2013 to 2017
$3.3M
California Breast Cancer Research CBCRP #21IB-0130National Science Foundation Graduate Research Fellowship Program 1144247NCI NIH HHS P01 CA154292NCI NIH HHS R01 CA166945NIH HHS P01CA154292NIH HHS R01CA166945
6 · The paper itself

Abstract

purposeWomen with radiographically dense or texturally complex breasts are at increased risk for interval cancer, defined as cancers diagnosed after a normal screening examination. The purpose of this study was to create masking measures and apply them to identify interval risk in a population of women who experienced either screen-detected or interval cancers after controlling for breast density.

methodsWe examined full-field digital screening mammograms acquired from 2006 to 2015. Examinations associated with 182 interval cancers were matched to 173 screen-detected cancers on age, race, exam date and time since last imaging examination. Local Image Quality Factor (IQF) values were calculated and used to create IQF maps that represented mammographic masking. We used various statistics to define global masking measures of these maps. Association of these masking measures with interval cancer vs screen-detected cancer was estimated using conditional logistic regression in a univariate and adjusted model for Breast Imaging-Reporting and Data System (BI-RADS) density. Receiver operator curves were calculated in each case to compare specificity vs sensitivity, and area under those curves were generated. Proportion of screen-detected cancer was estimated for stratifications of IQF features.

resultsSeveral masking features showed significant association with interval compared to screen-detected cancers after adjusting for BI-RADS density (up to P = 2.52E-6), and the 10th percentile of the IQF value (P = 1.72E-3) showed the strongest improvement in the area under the receiver operator curve, increasing from 0.65 using only BI-RADS density to 0.69. The highest masking group had a 32% proportion of screen-detected cancers while the low masking group had a 69% proportion.

conclusionsWe conclude that computer vision methods using model observers may improve quantifying the probability of breast cancer detection beyond using breast density alone.

Indexed as

Breast DensityArtifactsBreastBreast NeoplasmsCase-Control StudiesEarly Detection of CancerFemaleHumansImage Processing, Computer-AssistedMammographyPrognosisRisk AssessmentRisk Factorsbreastcancerdetectabilityintervalmammographymasking

Identifiers

PMID30697755
PMCPMC6416079

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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.