Evidence map›Paper›PMID 32108307›Full record

ArticleBreast cancer (Tokyo, Japan)2020

Male breast cancer: clinicopathological characterization of a National Danish cohort 1980-2009.

Anne Marie Bak Jylling, Vibeke Jensen, Giedrius Lelkaitis, Peer Christiansen, Sarah Schulz Nielsen, Marianne Djernes Lautrup

Abstract read
In one paragraph

Article in Breast cancer (Tokyo, Japan), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Comparison of male breast cancer in China and the US: a real-world cohort study.Translational breast cancer research : a journal focusing on translational research in breast cancer · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. HER2 Low Expression in Primary Male Breast Cancer.Breast cancer (Dove Medical Press) · 2024
    Article
  8. HRDrugs in context · 2023
    Review
  9. Review
  10. Review
  11. Article
  12. Article
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  14. 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

6 authors.

Anne Marie Bak JyllingResearch Unit of Pathology, Department of Clinical Research, University of Southern Denmark, Odense, Denmark. Anne.marie.bak.jylling@rsyd.dk.ORCID http://orcid.org/0000-0002-8071-549X
Vibeke JensenDepartment of Pathology, Aarhus University Hospital, Aarhus, Denmark.
Giedrius LelkaitisDepartment of Pathology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Peer ChristiansenDepartment of Plastic and Breast Surgery, Aarhus University Hospital, Aarhus, Denmark.
Sarah Schulz NielsenDanish Breast Cancer Group, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Marianne Djernes LautrupDepartment of Plastic and Breast Surgery, Aarhus University Hospital, Aarhus, Denmark.

Funding

Region of Southern Denmark R3-59
6 · The paper itself

Abstract

backgroundTo describe relevant pathological parameters of Danish male breast cancer patients (MBCP) diagnosed from 1980 to 2009, and to relate these data to treatment, overall survival (OS) and standardized mortality rate (SMR). MATERIALS AND

methodsThe MBCP cohort was defined from national Danish registers. A total of 643 MBCP were identified with tissue available in 457. Among these, 384 were primary operable. Where tissue blocks were available, tumor type, grade, estrogen receptor (ER), progesteron receptor (PgR) and androgen-receptor (AR) status as well as HER 2 and Ki67 were performed. OS was quantified by Kaplan-Meier estimates and SMR was calculated based on mortality rate among patients relative to the mortality rate in the general population.

resultsMale breast cancer was more often of ductal type, grade II and a very high proportion were ER and AR positive and HER2 negative. Intrinsic subtypes based on immunohistochemical evaluation showed luminal subtype. Ki67 ratio increased over period of study. OS declined by increased age, bigger tumor size, positive lymph node status, higher grade and Luminal B subtype. Hazard ratio and relative risk of SMR were highest for patients aged < 60 years.

conclusionMale breast cancer is of luminal subtype, but more often Luminal B. Ki67 is crucial in evaluation of subtypes by immunohistochemistry, but have limitations. Subtyping seems to be of major importance. AR also can have a role in future treatment.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Agents, AlkylatingBiomarkers, TumorBreastBreast Neoplasms, MaleChemotherapy, AdjuvantDenmarkErb-b2 Receptor Tyrosine KinasesFollow-Up StudiesHumansKaplan-Meier EstimateKi-67 AntigenMaleMastectomyAntineoplastic Agents, AlkylatingAR protein, humanBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesKi-67 AntigenMKI67 protein, humanReceptors, AndrogenClinicopathological characterizationIntrinsic subtypesMale breast cancerPathology

Identifiers

PMID32108307
PMCPMC7297815

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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.