Evidence map›Paper›PMID 41387529›Full record

ArticleScientific reports2025

Clinical characteristics and prognostic impact of HER2 low expression in breast cancer subtypes from a Brazilian real-world cohort.

André Mattar, Marcelo Antonini, Francisco Pimentel Cavalcante, Felipe Zerwes, Eduardo Camargo Millen, Fabricio Palermo Brenelli, Antônio Luiz Frasson, Marcelo Madeira, Marina Diógenes Teixeira, Andressa Gonçalves Amorim and 13 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. 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

23 authors.

André MattarCentro de Referência da Saúde da Mulher - Hospital da Mulher, Avenida Rio Branco, 1080, São Paulo, SP, 01206-001, Brazil. mattar.andre@gmail.com.ORCID https://orcid.org/0000-0001-5973-623X
Marcelo AntoniniBBREAST Group: Brazilian Breast Cancer Associate Research Team, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-1996-7428
Francisco Pimentel CavalcanteBBREAST Group: Brazilian Breast Cancer Associate Research Team, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-7156-2890
Felipe ZerwesBBREAST Group: Brazilian Breast Cancer Associate Research Team, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-1643-727X
Eduardo Camargo MillenBBREAST Group: Brazilian Breast Cancer Associate Research Team, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-2113-6324
Fabricio Palermo BrenelliBBREAST Group: Brazilian Breast Cancer Associate Research Team, São Paulo, Brazil.ORCID https://orcid.org/0000-0003-0589-1423
Antônio Luiz FrassonBBREAST Group: Brazilian Breast Cancer Associate Research Team, São Paulo, Brazil.ORCID https://orcid.org/0000-0003-1860-6898
Marcelo MadeiraFaculdade Israelita de Ciências da Saúde Albert Einstein, São Paulo, SP, Brazil.ORCID https://orcid.org/0000-0001-9429-3067
Marina Diógenes TeixeiraCentro de Referência da Saúde da Mulher - Hospital da Mulher, Avenida Rio Branco, 1080, São Paulo, SP, 01206-001, Brazil.ORCID https://orcid.org/0009-0001-7516-0215
Andressa Gonçalves AmorimHospital do Servidor Público Estadual Francisco Morato de Oliveira, São Paulo, SP, Brazil.ORCID https://orcid.org/0000-0002-3077-5873
Larissa Chrispim de OliveiraCentro de Referência da Saúde da Mulher - Hospital da Mulher, Avenida Rio Branco, 1080, São Paulo, SP, 01206-001, Brazil.ORCID https://orcid.org/0009-0009-6162-9463
Leonardo Ribeiro SoraresUniversidade Federal de Goias, Goiania, GO, Brazil.ORCID https://orcid.org/0000-0002-9448-6114
Gil FacinaUniversidade Federal de São Paulo, São Paulo, SP, Brazil.ORCID https://orcid.org/0000-0003-1418-0295
Rogerio FenileHospital Ipiranga, São Paulo, SP, Brazil.ORCID https://orcid.org/0000-0002-2352-8719
Ruffo Freitas-JúniorUniversidade Federal de Goias, Goiania, GO, Brazil.ORCID https://orcid.org/0000-0003-4145-8598
Renata ArakelianCentro de Referência da Saúde da Mulher - Hospital da Mulher, Avenida Rio Branco, 1080, São Paulo, SP, 01206-001, Brazil.ORCID https://orcid.org/0000-0002-6216-6327
Marcela Bonalumi Dos SantosCentro de Referência da Saúde da Mulher - Hospital da Mulher, Avenida Rio Branco, 1080, São Paulo, SP, 01206-001, Brazil.ORCID https://orcid.org/0009-0005-2272-5680
Henrique Lima CoutoRedimama - Redimasto, Belo Horizonte, MG, Brazil.ORCID https://orcid.org/0000-0002-3789-4461
Marcellus do Nascimento Moreira RamosHospital do Servidor Público Estadual Francisco Morato de Oliveira, São Paulo, SP, Brazil.ORCID https://orcid.org/0009-0007-5486-118X
Leandro Ladislau AlvesHead of Evidence Generation, Bristol Myers Squibb, São Paulo, Brazil.ORCID https://orcid.org/0000-0003-0664-9751
Júlio Antonio Pereira de AraújoCentro de Referência da Saúde da Mulher - Hospital da Mulher, Avenida Rio Branco, 1080, São Paulo, SP, 01206-001, Brazil.ORCID https://orcid.org/0000-0001-6706-2589
Renata Montarroyos LeiteOncoclínicas, São Paulo, Brazil.ORCID https://orcid.org/0009-0008-1211-2823
Luiz Henrique GebrimHospital Beneficência Portuguesa, São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0001-9941-9191

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer (BC) is the most prevalent cancer among Brazilian women, yet related data remain limited. The HER2-low classification has gained significance with the advent of targeted therapies. This study aimed to assess survival outcomes of HER2-low BC compared to other subtypes in a real-world Brazilian cohort. We analyzed data from 8,485 breast cancer patients treated at Pérola Byington Hospital between 2010 and 2019. Overall survival (OS) was the primary endpoint, stratified by cancer subtype. The t-test and chi-square test evaluated variable associations, while multivariate analysis calculated odds ratios and 95% confidence intervals. Cox regression assessed survival, and Kaplan-Meier curves illustrated OS differences. The patients with HER2-low breast cancers showed significantly better overall survival than those with the triple-negative subtype (p < 0.01). However, they had significantly poorer overall survival than those with the Luminal A-like subtype (p < 0.01). The patients with triple-negative HER2-low disease had a higher risk of mortality than those with HER2-0 (p < 0.01). Finally, patients who achieved pathological complete response experienced significantly better overall survival than those who did not (p < 0.01). Our findings highlight triple negative HER2-low BC as a distinct subtype identifiable via standard immunohistochemistry, beyond just biomarker status. The study underscores the prognostic diversity among BC subtypes and emphasizes the importance of personalized treatment strategies.

Indexed as

Breast NeoplasmsErb-b2 Receptor Tyrosine KinasesAdultAgedBiomarkers, TumorBrazilCohort StudiesFemaleHumansKaplan-Meier EstimateMiddle AgedPrognosisBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesHER2-low breast cancerPrognostic implicationsReal-world dataSurvival outcomes

Identifiers

PMID41387529
PMCPMC12804669

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LicenceCC BY-NC-ND
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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.