Evidence map›Paper›PMID 27657341›Full record

ArticleBritish journal of cancer2016

The combined endocrine receptor in breast cancer, a novel approach to traditional hormone receptor interpretation and a better discriminator of outcome than ER and PR alone.

Esther J Campbell, Mathias Tesson, Flora Doogan, Zahra M A Mohammed, Elizabeth Mallon, Joanne Edwards

Open access · hybridAbstract readComparative StudyValidation Study
In one paragraph

Article in British journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
3.9field-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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Esther J CampbellDepartment of Surgery, Queen Elizabeth University Hospital, Glasgow G51 4TF, UK.
Mathias TessonInstitute of Cancer Sciences, University of Glasgow, Wolfson Wohl Translational Cancer Research Centre, Garscube Estate, Glasgow G61 1HQ, UK.
Flora DooganDepartment of Surgery, Queen Elizabeth University Hospital, Glasgow G51 4TF, UK.
Zahra M A MohammedInstitute of Cancer Sciences, University of Glasgow, Wolfson Wohl Translational Cancer Research Centre, Garscube Estate, Glasgow G61 1HQ, UK.
Elizabeth MallonDepartment of Pathology, Queen Elizabeth University Hospital, Glasgow G51 4TF, UK.
Joanne EdwardsInstitute of Cancer Sciences, University of Glasgow, Wolfson Wohl Translational Cancer Research Centre, Garscube Estate, Glasgow G61 1HQ, UK.
Queen Elizabeth University Hospital · GBUniversity of Glasgow · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe functional role of progesterone receptor (PR) signalling was previously unclear and PR testing in breast cancer is controversial. Recent defining work has highlighted the functional crosstalk that exists between the oestrogen receptor (ER) and PR. The purpose of this retrospective cohort study was to compare the prognostic value of the combined ER and PR score with either ER or PR alone.

methodsTumour Allred ER and PR scores were reclassified as negative, low and high. The combined endocrine receptor (CER) was calculated as the average of the reclassified ER and PR scores, resulting in three groups: CER negative, impaired and high. Cox proportional hazards models were used to estimate disease-free survival (DFS) and breast cancer-specific survival (BCSS).

resultsThe CER was a more powerful predictor of 5-year DFS and BCSS than either ER or PR alone. In multivariate analysis that included ER, PR and CER, only CER remained an independent prognostic variable for 5-year DFS (hazard ratio (HR) 0.393; CI: 0.283-0.548, P=0.00001) and BCSS (HR 0.553; CI: 0.423-0.722; P=2.506 × 10

conclusionsCombined endocrine receptor is a more powerful discriminator of patient outcome than either ER or PR alone. Economical and simple, it can identify risk in ER+ early breast cancer and potentially be used for adjuvant cytotoxic chemotherapy decision-making.

Indexed as

EstrogensProgesteroneAdultAgedBreast NeoplasmsCarcinomaChemotherapy, AdjuvantDisease-Free SurvivalErb-b2 Receptor Tyrosine KinasesFollow-Up StudiesHumansKaplan-Meier EstimateMiddle AgedNeoplasms, Hormone-DependentPrognosisProportional Hazards ModelsErb-b2 Receptor Tyrosine KinasesEstrogensProgesteroneReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID27657341
PMCPMC5061898
OpenAlexW2429598957

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.