Evidence map›Paper›PMID 37197610›Full record

ArticleBreast cancer (Dove Medical Press)2023

Androgen Receptor Status in Triple Negative Breast Cancer: Does It Correlate with Clinicopathological Characteristics?

Alex L Dubrava, Pan Su Pyae Kyaw, Joseph Newman, Jarrad Pringle, Justin Westhuyzen, Gina La Hera Fuentes, Thomas P Shakespeare, Renukadas Sakalkale, Noel J Aherne

Open access · goldAbstract read
In one paragraph

Article in Breast cancer (Dove Medical Press), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Genomic Alterations in Quadruple-Negative Breast Cancer Tumors.International journal of molecular sciences · 2026
    Article
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  11. Triple-negative breast cancer: from classical clinicopathological features to androgen receptor profile.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

9 authors at 2 institutions in 1 country.

Alex L DubravaDepartment of Radiation Oncology, Mid North Coast Cancer Centre, Coffs Harbour, New South Wales, Australia.ORCID 0000-0002-2931-9969
Pan Su Pyae KyawDepartment of Radiation Oncology, Mid North Coast Cancer Centre, Coffs Harbour, New South Wales, Australia.ORCID 0009-0008-6783-9720
Joseph NewmanDepartment of Radiation Oncology, Mid North Coast Cancer Centre, Coffs Harbour, New South Wales, Australia.ORCID 0000-0002-3263-2841
Jarrad PringleDepartment of Radiation Oncology, Mid North Coast Cancer Centre, Coffs Harbour, New South Wales, Australia.
Justin WesthuyzenSchool of Health and Human Sciences, Southern Cross University, Coffs Harbour, New South Wales, Australia.ORCID 0000-0002-4812-8973
Gina La Hera FuentesCoffs Harbour Rural Clinical School, University of New South Wales, Coffs Harbour Health Campus, Coffs Harbour, New South Wales, Australia.
Thomas P ShakespeareDepartment of Radiation Oncology, Mid North Coast Cancer Centre, Coffs Harbour, New South Wales, Australia.
Renukadas SakalkaleCoffs Harbour Rural Clinical School, University of New South Wales, Coffs Harbour Health Campus, Coffs Harbour, New South Wales, Australia.
Noel J AherneDepartment of Radiation Oncology, Mid North Coast Cancer Centre, Coffs Harbour, New South Wales, Australia.
Coffs Harbour City Council · AUSouthern Cross University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Triple negative breast cancer (TNBC) is a breast carcinoma subtype that neither expresses estrogen (ER) and progesterone receptors (PR) nor the human epidermal growth factor receptor 2 (HER2). Patients with TNBC have been shown to have poorer outcomes mainly owing to the limited treatment options available. However, some studies have shown TNBC tumors expressing androgen receptors (AR), raising hopes of its prognostic role. Patients and Methods: This retrospective study investigated the expression of AR in TNBC and its relationship with known patient demographics, tumor and survival characteristics. From the records of 205 TNBC patients, 36 had available archived tissue samples eligible for AR staining. For statistical purposes, tumors were classified as either "positive" or "negative" for AR expression. The nuclear expression of AR was scored by measuring the percentage of stained tumor cells and its staining intensity. Results: AR was expressed by 50% of the tissue samples in our TNBC cohort. The relationship between AR status with age at the time of TNBC diagnosis was statistically significant, with all AR positive TNBC patients being greater than 50 years old (vs 72.2% in AR negative TNBC). Also, the relationship between AR status and type of surgery received was statistically significant. There were no statistically significant associations between AR status with other tumor characteristics including "TNM status", tumor grade or treatments received. There was no statistically significant difference in median survival between AR negative and AR positive TNBC patients (3.5 vs 3.1 years; p = 0.581). The relationship between OS time and AR status (p = 0.581), type of surgery (p = 0.061) and treatments (p = 0.917) were not statistically significant. Conclusion: The androgen receptor may be an important prognostic marker in TNBC, with further research warranted. This research may benefit future studies investigating receptor-targeted therapies in TNBC.

Indexed as

androgen receptorbreast cancertriple negative

Identifiers

PMID37197610
PMCPMC10184857
OpenAlexW4376104792

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.