Evidence map›Paper›PMID 31004391›Full record

ReviewJournal of magnetic resonance imaging : JMRI2020

Background parenchymal enhancement on breast MRI: A comprehensive review.

Geraldine J Liao, Leah C Henze Bancroft, Roberta M Strigel, Rhea D Chitalia, Despina Kontos, Linda Moy, Savannah C Partridge, Habib Rahbar

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Journal of magnetic resonance imaging : JMRI, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06629896 (Comparison Between Contrast-Enhanced Mammography and Magnetic Resonance Imaging in the Surveillance of High-Risk Women for Breast Cancer), which is not on this map. Cited by 75 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 3 pooled it
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.

NCT06629896 narecruitingnot on this mapstarted 2025, after this paper: background citation

Comparison Between Contrast-Enhanced Mammography and Magnetic Resonance Imaging in the Surveillance of High-Risk Women for Breast Cancer: The Randomized Controlled Trial 'Con-trust. Funded by European Commission NextGenerationEU - Ministero Della Salute PNRR: M6/C2_CALL 2023 Full Proposal

TypeinterventionalSponsorAzienda USL Reggio Emilia - IRCCSRan2025 to 2030Enrolled2,200ConditionsBreast Cancer Screening and DiagnosisArmsContrast Enhancement Mammography, magnetic resonance imaging (MRI) and digital mammography (DM)
3 · Its place in the literature

Who cites it

75 citing papers in PubMed, 3 syntheses or guidelines pooled it, 126 citations in OpenAlex.

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15 more citing papers are in PubMed but not listed here.

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 5 institutions in 1 country.

Geraldine J LiaoDepartment of Radiology, University of Washington School of Medicine, Seattle, Washington, USA.
Leah C Henze BancroftDepartment of Radiology, University of Wisconsin, Madison, Wisconsin, USA.
Roberta M StrigelDepartment of Radiology, University of Wisconsin, Madison, Wisconsin, USA.
Rhea D ChitaliaDepartment of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Despina KontosDepartment of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Linda MoyDepartment of Radiology, New York University School of Medicine, New York, New York, USA.
Savannah C PartridgeDepartment of Radiology, University of Washington School of Medicine, Seattle, Washington, USA.
Habib RahbarDepartment of Radiology, University of Washington School of Medicine, Seattle, Washington, USA.ORCID 0000-0003-4835-1478
University of Pennsylvania · USUniversity of Washington · USUniversity of Wisconsin–Madison · USNew York University · USVirginia Mason Medical Center · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Christian Capitini · 1985 to 2026
$142.6M
TR&D 4: Revealing Microstructure: Biophysical modeling and validation for discovery and clinical careP41EB017183 · NIBIB · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Christopher M Collins · 2014 to 2026
$19.3M
DCE MRI Study for Breast Cancer.R01CA160620 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI KIM, SUNGHEON GENE · 2012 to 2023
$5.4M
Validation and Standardization of the Apparent Diffusion Coefficient as a Quantitative Imaging Biomarker in Breast CancerR01CA207290 · NCI · UNIVERSITY OF WASHINGTON · PI PARTRIDGE, SAVANNAH CORRINA · 2017 to 2022
$2.2M
MRI Characterization of Biological Risk of Ductal Carcinoma in SituR01CA203883 · NCI · UNIVERSITY OF WASHINGTON · PI RAHBAR, HABIBOLLAH · 2017 to 2021
$1.8M
NCI NIH HHS P30 CA014520NCI NIH HHS R01 CA160620NCI NIH HHS R01 CA203883NCI NIH HHS R01 CA207290NIBIB NIH HHS P41 EB017183
6 · The paper itself

Abstract

The degree of normal fibroglandular tissue that enhances on breast MRI, known as background parenchymal enhancement (BPE), was initially described as an incidental finding that could affect interpretation performance. While BPE is now established to be a physiologic phenomenon that is affected by both endogenous and exogenous hormone levels, evidence supporting the notion that BPE frequently masks breast cancers is limited. However, compelling data have emerged to suggest BPE is an independent marker of breast cancer risk and breast cancer treatment outcomes. Specifically, multiple studies have shown that elevated BPE levels, measured qualitatively or quantitatively, are associated with a greater risk of developing breast cancer. Evidence also suggests that BPE could be a predictor of neoadjuvant breast cancer treatment response and overall breast cancer treatment outcomes. These discoveries come at a time when breast cancer screening and treatment have moved toward an increased emphasis on targeted and individualized approaches, of which the identification of imaging features that can predict cancer diagnosis and treatment response is an increasingly recognized component. Historically, researchers have primarily studied quantitative tumor imaging features in pursuit of clinically useful biomarkers. However, the need to segment less well-defined areas of normal tissue for quantitative BPE measurements presents its own unique challenges. Furthermore, there is no consensus on the optimal timing on dynamic contrast-enhanced MRI for BPE quantitation. This article comprehensively reviews BPE with a particular focus on its potential to increase precision approaches to breast cancer risk assessment, diagnosis, and treatment. It also describes areas of needed future research, such as the applicability of BPE to women at average risk, the biological underpinnings of BPE, and the standardization of BPE characterization. Level of Evidence: 3 Technical Efficacy Stage: 5 J. Magn. Reson. Imaging 2020;51:43-61.

Indexed as

BreastBreast NeoplasmsFemaleHumansImage Interpretation, Computer-AssistedMagnetic Resonance Imagingbackground parenchymal enhancementbiomarkersbreast cancer riskbreast MRIfibroglandular tissueprecision medicine

Identifiers

PMID31004391
PMCPMC7207072
OpenAlexW2939007418

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.