Evidence map›Paper›PMID 30140962›Full record

ArticleBreast cancer research and treatment2018

Histopathologic characteristics of background parenchymal enhancement (BPE) on breast MRI.

Janice S Sung, Adriana D Corben, Jennifer D Brooks, Marcia Edelweiss, Delia M Keating, Christine Lin, Elizabeth A Morris, Prusha Patel, Mark Robson, Meghan Woods and 2 more

Open access · greenAbstract read
In one paragraph

Article in Breast cancer research and treatment, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Observational
  6. Article
  7. Breast MRI to Screen Women With Extremely Dense Breasts.Journal of magnetic resonance imaging : JMRI · 2025
    Review
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  19. Review
  20. Background parenchymal enhancement on breast MRI: A comprehensive review.Journal of magnetic resonance imaging : JMRI · 2020
    Review
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

12 authors at 3 institutions in 2 countries.

Janice S SungDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Adriana D CorbenDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Jennifer D BrooksDepartment of Epidemiology, Dalla Lana School of Public Health, University of Toronto, Toronto, Canada.
Marcia EdelweissDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Delia M KeatingDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Christine LinDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, 485 Lexington Avenue, Room 2061, New York, NY, 10017, USA.
Elizabeth A MorrisDepartment of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Prusha PatelDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, 485 Lexington Avenue, Room 2061, New York, NY, 10017, USA.
Mark RobsonDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Meghan WoodsDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, 485 Lexington Avenue, Room 2061, New York, NY, 10017, USA.
Jonine L BernsteinDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, 485 Lexington Avenue, Room 2061, New York, NY, 10017, USA.
Malcolm C PikeDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, 485 Lexington Avenue, Room 2061, New York, NY, 10017, USA. pikem@mskcc.org.
Memorial Sloan Kettering Cancer Center · USIcahn School of Medicine at Mount Sinai · USUniversity of Toronto · CA

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
MRI Background Parenchymal Enhancement as a Risk Factor for Breast CancerR01CA183086 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI BERNSTEIN, JONINE L., PIKE, MALCOLM C · 2014 to 2016
$2.1M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA183086
6 · The paper itself

Abstract

purposeBreast fibroglandular tissue (FGT), as visualized on a mammogram (mammographic density, MD), is one of the strongest known risk factors for breast cancer. FGT is also visible on breast MRI, and increased background parenchymal enhancement (BPE) in the FGT has been identified as potentially a major breast cancer risk factor. The aim of this exploratory study was to examine the biologic basis of BPE.

methodsWe examined the unaffected contra-lateral breast of 80 breast cancer patients undergoing a prophylactic mastectomy before any treatment other than surgery of their breast cancer. BPE was classified on the BI-RADS scale (minimal/mild/moderate/marked). Slides were stained for microvessel density (MVD), CD34 (another measure of endothelial density), glandular tissue within the FGT and VEGF. Spearman correlations were used to evaluate the associations between BPE and these pathologic variables.

resultsIn pre-menopausal patients, BPE was highly correlated with MVD, CD34 and glandular concentration within the FGT, and the pathologic variables were themselves highly correlated. The expression of VEGF was effectively confined to terminal duct lobular unit (TDLU) epithelium. The same relationships of the four pathologic variables with BPE were seen in post-menopausal patients, but the relationships were much weaker and not statistically significant.

conclusionThe strong correlation of BPE and MVD together with the high correlation of MVD with glandular concentration seen in pre-menopausal patients indicates that increased breast cancer risk associated with BPE in pre-menopausal women is likely to result from its association with increased concentration of glandular tissue in the FGT. The effective confinement of VEGF expression to the TDLUs shows that the signal for MVD growth arises directly from the glandular tissue. Further studies are needed to understand the basis of BPE in post-menopausal women.

Indexed as

Magnetic Resonance ImagingAdultBreastBreast DensityBreast NeoplasmsFemaleHumansMammographyMiddle AgedParenchymal TissueRisk FactorsBackground parenchymal enhancementBreast MRIFibroglandular tissueImmunohistochemistryMicrovessel densityVEGF

Identifiers

PMID30140962
PMCPMC6697118
OpenAlexW2888692682

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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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.