Evidence map›Paper›PMID 32928183›Full record

ArticleBMC women's health2020

Androgen receptor expression in a Sri Lankan patient cohort with early breast carcinoma.

Harshima Disvini Wijesinghe, Gayani Kokila Wijesinghe, Zahara Mansoor, Sanjeev Vigneshwara, Janakie Fernando, Dehan Gunasekera, Menaka Dilani Samarawickrama Lokuhetty

Open access · goldAbstract read
In one paragraph

Article in BMC women's health, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 89% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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 3 institutions in 1 country.

Harshima Disvini WijesingheDepartment of Pathology, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka. harshima@path.cmb.ac.lk.ORCID 0000-0002-2847-1440
Gayani Kokila WijesingheDepartment of Pathology, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka.
Zahara MansoorDepartment of Pathology, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka.
Sanjeev VigneshwaraDepartment of Pathology, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka.
Janakie FernandoDepartment of Pathology, National of Hospital of Sri Lanka, Colombo, Sri Lanka.
Dehan GunasekeraApeksha Hospital, Maharagama, Sri Lanka.
Menaka Dilani Samarawickrama LokuhettyDepartment of Pathology, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka.
University of Colombo · LKNational Cancer Institute of Sri Lanka · LKNational Hospital of Sri Lanka · LK

Funding

Kumi and Heram Bilmoria Trust Fund PT/8/2/42/C/581/TR/02National Research Council Sri Lanka 11:51
6 · The paper itself

Abstract

backgroundAndrogen receptor (AR) expression is emerging as a prognostic biomarker in breast carcinoma (BCa). The study aimed to determine the prevalence of AR expression by immunohistochemical analysis among a cohort of Sri Lankan women with early BCa and to evaluate its association with clinicopathological features including immunohistochemical molecular subtype and early survival.

methodWe studied the clinical and pathological features and immunohistochemical profile of 141 women undergoing primary surgery for early BCa, followed by standard adjuvant therapy. AR status was assessed by immunohistochemistry in all cases. Overall survival (OS) and disease-free survival (DFS) was determined. The relationship between AR expression and clinical and pathological parameters and immunohistochemical molecular subtype was analyzed using Student T test and chi-square tests. Cox regression analysis was used to analyze the prognostic impact of AR expression.

resultsAR expression was seen in 40.8%(95%CI 33.10-49.07%) of the BCa study cohort. None of the clinical data studied showed a significant association with the AR status(p > 0.05). Ductal carcinoma in situ(p = 0.003), oestrogen receptor (ER) (p = 0.001) and progesterone receptor (PR) (p = 0.001) positivity and luminal IHC molecular subtype(p = 0.016) were significantly associated with AR-positive status. AR-negative status was significantly associated with tumour necrosis > 50%(p = 0.031), moderate to extensive lymphocytic infiltrate at the tumour margin(p = 0.025) and basal triple negative breast carcinoma(p = 0.016). The mean duration of patient follow-up was 46.70(95% CI 46.495-46.905) months (3.89 years). On univariate analysis, AR-positivity was associated with better OS among ER-positive tumours(p = 0.047), specifically in postmenopausal women (p = 0.030). In ER-negative tumours, AR positivity was associated with worse DFS (p = 0.036). On multivariate analysis, TNM stage and ER/AR status were predictive of survival. ER-positive/AR-positive (ER+/AR+) tumours demonstrated better OS than ER-positive/AR-negative (ER+/AR-) tumours(p = 0.015). ER-negative/AR-positive (ER-/AR+) tumours (p = 0.014) had a worse DFS than ER-negative/AR-negative (ER-/AR-) tumours.

conclusionsAR prevalence obtained was low. AR positivity was associated with positivity for ER and PR. On multivariate analysis, apart from TNM stage only ER/AR status were predictive of OS and DFS, with concordant expression of ER/AR demonstrating a better, early survival.

Indexed as

AdultAgedAndrogensBiomarkers, TumorBreast NeoplasmsDisease-Free SurvivalErb-b2 Receptor Tyrosine KinasesFemaleHumansImmunohistochemistryMastectomyMiddle AgedPrevalencePrognosisReceptors, AndrogenReceptors, EstrogenAndrogensBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesReceptors, AndrogenReceptors, EstrogenReceptors, ProgesteroneAndrogen receptorsBreast carcinomaClinicopathological featuresPrevalencePrognosisSri Lanka

Identifiers

PMID32928183
PMCPMC7490868
OpenAlexW3085439208

What OpenQuestion holds

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LicenceCC BY
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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.