Evidence map›Paper›PMID 35933487›Full record

ArticleBreast cancer research and treatment2022

Correlation of tumour subtype with long-term outcome in small breast carcinomas: a Swedish population-based retrospective cohort study.

Gunilla Rask, Anoosheh Nazemroaya, Malin Jansson, Charlotta Wadsten, Greger Nilsson, Carl Blomqvist, Lars Holmberg, Fredrik Wärnberg, Malin Sund

Open access · hybridAbstract read
In one paragraph

Article in Breast cancer research and treatment, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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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 5 institutions in 3 countries.

Gunilla RaskDepartment of Medical Biosciences/Pathology, Umeå University, Umeå, Sweden. gunilla.rask@umu.se.ORCID http://orcid.org/0000-0002-0829-896X
Anoosheh NazemroayaDepartment of Medical Biosciences/Pathology, Umeå University, Umeå, Sweden.
Malin JanssonDepartment of Surgery and Perioperative Sciences/Surgery, Umeå University, Umeå, Sweden.
Charlotta WadstenDepartment of Surgery and Perioperative Sciences/Surgery, Umeå University, Umeå, Sweden.
Greger NilssonDepartment of Immunology, Genetics and Pathology, Section of Experimental and Clinical Oncology, Uppsala University, University Hospital, Uppsala, Sweden.
Carl BlomqvistDepartment of Oncology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Lars HolmbergTranslational Oncology and Urology Research (TOUR), School of Cancer and Pharmaceutical Sciences, King's College London, London, UK.
Fredrik WärnbergDepartment of Clinical Sciences, Department of Surgery, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Malin SundDepartment of Surgery and Perioperative Sciences/Surgery, Umeå University, Umeå, Sweden.
Umeå University · SEUniversity of Helsinki · FIUniversity of Gothenburg · SEUppsala University · SEUppsala University Hospital · SE

Funding

Västerbotten Läns Landsting ALF-medelVisare Norr VISARENORR750491Visare Norr VISARENORR931408
6 · The paper itself

Abstract

purposeTo investigate if molecular subtype is associated with outcome in stage 1 breast cancer (BC).

methodsTissue samples from 445 women with node-negative BC ≤ 15 mm, treated in 1986-2004, were classified into surrogate molecular subtypes [Luminal A-like, Luminal B-like (HER2-), HER2-positive, and triple negative breast cancer (TNBC)]. Information on treatment, recurrences, and survival were gathered from medical records.

resultsTumour subtype was not associated with overall survival (OS). Luminal B-like (HER2-) and TNBC were associated with higher incidence of distant metastasis at 20 years (Hazard ratio (HR) 2.26; 95% CI 1.08-4.75 and HR 3.24; 95% CI 1.17-9.00, respectively). Luminal B-like (HER2-) and TNBC patients also had worse breast cancer-specific survival (BCSS), although not statistically significant (HR 1.53; 95% CI 0.70-3.33 and HR 1.89; 95% CI 0.60-5.93, respectively). HER2-positive BC was not associated with poor outcome despite no patient receiving HER2-targeted therapy, with most of these tumours being ER+.

conclusionsStage 1 TNBC or Luminal B-like (HER2-) tumours behave more aggressively. Women with HER2+/ER+ tumours do not have an increased risk of distant metastasis or death, absent targeted treatment.

Indexed as

Breast NeoplasmsCarcinomaTriple Negative Breast NeoplasmsBiomarkers, TumorCohort StudiesErb-b2 Receptor Tyrosine KinasesFemaleHumansPrognosisReceptors, ProgesteroneRetrospective StudiesSwedenBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesReceptors, ProgesteroneBreast cancerLong-term outcomeMolecular subtypesTMA

Identifiers

PMID35933487
PMCPMC9464733
OpenAlexW4290058945

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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.