Evidence map›Paper›PMID 25522915›Full record

ArticleDiagnostic pathology2014

Breast cancer stromal elastosis is associated with mammography screening detection, low Ki67 expression and favourable prognosis in a population-based study.

Ying Chen, Tor A Klingen, Elisabeth Wik, Hans Aas, Einar Vigeland, Knut Liestøl, Øystein Garred, Jan Mæhlen, Lars A Akslen, Jon Lømo

Open access · goldAbstract read
In one paragraph

Article in Diagnostic pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

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  8. Elastosis in ERα-positive male breast cancer.Virchows Archiv : an international journal of pathology · 2021
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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

10 authors at 5 institutions in 1 country.

Ying ChenDepartment of Pathology, Vestfold Hospital, Tønsberg, Norway. ying.chen@ahus.no.
Tor A KlingenDepartment of Pathology, Vestfold Hospital, Tønsberg, Norway. tor.klingen@siv.no.
Elisabeth WikCentre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Section for Pathology, University of Bergen, Bergen, Norway. elisabeth.wik@k1.uib.no.
Hans AasDepartment of Surgery, Vestfold Hospital, Tønsberg, Norway. hans.aas@siv.no.
Einar VigelandDepartment of Radiology, Vestfold Hospital, Tønsberg, Norway. einar.vigeland@siv.no.
Knut LiestølInstitute of Informatics, University of Oslo, Oslo, Norway. knut@ifi.uio.no.
Øystein GarredDepartment of Pathology, Oslo University Hospital, 0424, Oslo, Norway. UXYSGA@ous-hf.no.
Jan MæhlenDepartment of Pathology, Oslo University Hospital, 0424, Oslo, Norway. jan.mahlen@medisin.uio.no.
Lars A AkslenCentre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, Section for Pathology, University of Bergen, Bergen, Norway. lars.akslen@k1.uib.no.
Jon LømoDepartment of Pathology, Oslo University Hospital, 0424, Oslo, Norway. jon.lomo@ous-hf.no.
Oslo University Hospital · NOSykehuset i Vestfold · NOHaukeland University Hospital · NOAkershus University Hospital · NOUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMammography screen-detected breast cancers have a better prognosis than predicted from established prognostic markers. A search for additional features that are characteristic for these tumours and their prognosis is needed to reduce overtreatment, a recognized challenge in breast cancer patient management today. Here, we have investigated the occurrence and importance of tumour elastosis.

methodsWe performed a population based retrospective study of breast cancers detected in the Norwegian Breast Cancer Screening Programme in Vestfold County during 2004-2009. In total, 197 invasive screen-detected cancers and 75 interval cancers in patients aged 50-69 years were compared with regard to standard clinico-pathological parameters and tumour shape, as well as ER, PR, HER2 and Ki67 expression. In particular, the presence of elastotic material in tumours was graded on a 4-tiered scale (score 0-3).

resultsScreen-detected cancers had a significantly higher content of stromal elastosis than interval cancers (p < 0.001). High content of elastosis (score 3) correlated strongly with stellate tumour shape, low histological grade, and ER+/HER2- status. Further, high elastosis score was significantly associated with lower Ki67 expression. In survival analyses, cases with high elastosis demonstrated increased recurrence free (p = 0.03) and disease-specific survival (p = 0.11) compared to cases with low elastosis.

conclusionThere is a strong correlation between the presence of tumour elastosis, stellate tumour shape and mammography detection of breast cancers. To our knowledge, this is the first time elastosis has been studied in relation to breast cancer detection method. Presence of elastosis is associated with low tumour cell proliferation (Ki67) and a good prognosis. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/13000_2014_230.

Indexed as

Elastic TissueMammographyStromal CellsAgedBreast NeoplasmsDisease-Free SurvivalElastinFemaleHumansKaplan-Meier EstimateKi-67 AntigenMiddle AgedNeoplasm GradingNeoplasm Recurrence, LocalNorwayPredictive Value of TestsElastinKi-67 Antigen

Identifiers

PMID25522915
PMCPMC4300053
OpenAlexW2130067006

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.