Evidence map›Paper›PMID 28286675›Full record

ArticleInternational journal of breast cancer2017

Ductal Breast Carcinoma In Situ: Mammographic Features and Its Relation to Prognosis and Tumour Biology in a Population Based Cohort.

Wenjing Zhou, Thomas Sollie, Tibor Tot, Carl Blomqvist, Shahin Abdsaleh, Göran Liljegren, Fredrik Wärnberg

Open access · goldAbstract read
In one paragraph

Article in International journal of breast cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. How much do we know about the metastatic process?Clinical & experimental metastasis · 2024
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  6. Elastic stains in the evaluation of DCIS with comedo necrosis in breast cancers.Virchows Archiv : an international journal of pathology · 2018
    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

7 authors at 5 institutions in 2 countries.

Wenjing ZhouDepartment of Surgical Sciences, Uppsala University, Uppsala Academic Hospital, Uppsala, Sweden.ORCID 0000-0002-1312-6337
Thomas SollieDepartment of Pathology, Örebro University, Örebro, Sweden.
Tibor TotDepartment of Pathology, Falun Central Hospital, Falun, Sweden.ORCID 0000-0001-8479-0115
Carl BlomqvistDepartment of Oncology, Helsinki University Central Hospital, Helsinki, Finland.
Shahin AbdsalehDepartment of Radiology, Oncology and Radiation Science, Uppsala University, Uppsala, Sweden.
Göran LiljegrenDepartment of Surgery, Örebro University, Örebro, Sweden.
Fredrik WärnbergDepartment of Surgical Sciences, Uppsala University, Uppsala Academic Hospital, Uppsala, Sweden.ORCID 0000-0002-0130-7296
Örebro University · SEUppsala University Hospital · SEFalun Hospital · SEHelsinki University Hospital · FIUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Casting-type calcifications and a histopathological picture with cancer-filled duct-like structures have been presented as breast cancer with neoductgenesis. We correlated mammographic features and histopathological neoductgenesis with prognosis in a DCIS cohort with long follow-up. Mammographic features were classified into seven groups according to Tabár. Histopathological neoductgenesis was defined by concentration of ducts, lymphocyte infiltration, and periductal fibrosis. Endpoints were ipsilateral (IBE) in situ and invasive events. Casting-type calcifications and neoductgenesis were both related to high nuclear grade, ER- and PR-negativity, and HER2 overexpression but not to each other. Casting-type calcifications and neoductgenesis were both related to a nonsignificant lower risk of invasive IBE, HR 0.38 (0.13-1.08) and 0.82 (0.29-2.27), respectively, and the HR of an in situ IBE was 0.90 (0.41-1.95) and 1.60 (0.75-3.39), respectively. Casting-type calcifications could not be related to a worse prognosis in DCIS. We cannot explain why a more aggressive phenotype of DCIS did not correspond to a worse prognosis. Further studies on how the progression from in situ to invasive carcinoma is driven are needed.

Identifiers

PMID28286675
PMCPMC5329681
OpenAlexW2588365983

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.