Evidence map›Paper›PMID 36563519›Full record

ArticleESMO open2023

Influence of HER2 expression on prognosis in metastatic triple-negative breast cancer-results from an international, multicenter analysis coordinated by the AGMT Study Group.

S P Gampenrieder, V Dezentjé, M Lambertini, A de Nonneville, M Marhold, F Le Du, A Cortés Salgado, D Alpuim Costa, M Vaz Batista, N Chic Ruché and 22 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in ESMO open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
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  14. Challenges in HER2-low breast cancer identification, detection, and treatment.Translational breast cancer research : a journal focusing on translational research in breast cancer · 2024
    Review
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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

32 authors at 18 institutions in 8 countries.

S P GampenriederSalzburg Cancer Research Institute- Center for Clinical Cancer and Immunology Trials, Salzburg, Austria; Cancer Cluster Salzburg, Salzburg, Austria; IIIrd Medical Department with Haematology, Medical Oncology, Haemostaseology, Infectiology and Rheumatology, Oncologic Center, Paracelsus Medical University Salzburg, Salzburg, Austria.
V DezentjéDepartment of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
M LambertiniMedical Oncology Department, U.O.C. Clinica di Oncologia Medica, IRCCS Ospedale Policlinico San Martino Genova, Genova, Italy; Department of Internal Medicine and Medical Specialties (DiMI), School of Medicine, Università di Genova, Genova, Italy.
A de NonnevilleDepartment of Medical Oncology, Institut Paoli-Calmettes, Aix-Marseille Univ, CNRS, INSERM, Marseille, France.
M MarholdDepartment of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.
F Le DuDépartement d'oncologie médicale, Centre Eugène-Marquis, Rennes, France.
A Cortés SalgadoMedical Oncology Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.
D Alpuim CostaHaematology and Oncology Department, CUF Oncologia, Lisbon, Portugal; NOVA Medical School, (NMS), Faculdade de Ciências Médicas (FCM), Lisbon, Portugal; Centro de Medicina Subaquática e Hiperbárica (CMSH), Marinha Portuguesa, Lisbon, Portugal.
M Vaz BatistaOncology Department, Hospital Professor Doutor Fernando Fonseca, Amadora, Portugal.
N Chic RuchéDepartment of Medical Oncology, Hospital Clínic Barcelona, Barcelona, Spain.
C TinchonDepartment for Haemato-Oncology, LKH Hochsteiermark-Leoben, Leoben, Austria.
A PetzerInternal Medicine I for Hematology with Stem Cell Transplantation, Hemostaseology and Medical Oncology, Ordensklinikum Linz Barmherzige Schwestern-Elisabethinen, Linz, Austria.
E BlondeauxU.O. Epidemiology Unit, IRCCS Ospedale Policlinico San Martino Genova, Genova, Italy.
L Del MastroMedical Oncology Department, U.O.C. Clinica di Oncologia Medica, IRCCS Ospedale Policlinico San Martino Genova, Genova, Italy; Department of Internal Medicine and Medical Specialties (DiMI), School of Medicine, Università di Genova, Genova, Italy.
G TargatoDipartimento di Oncologia, Ospedale Santa Maria della Misericordia di Udine, Udine, Italy.
F BertucciDepartment of Medical Oncology, Institut Paoli-Calmettes, Aix-Marseille Univ, CNRS, INSERM, Marseille, France.
A GonçalvesDepartment of Medical Oncology, Institut Paoli-Calmettes, Aix-Marseille Univ, CNRS, INSERM, Marseille, France.
F ViretDepartment of Medical Oncology, Institut Paoli-Calmettes, Aix-Marseille Univ, CNRS, INSERM, Marseille, France.
R BartschDepartment of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.
C MannsbartDepartment of Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria.
A DeleuzeDépartement d'oncologie médicale, Centre Eugène-Marquis, Rennes, France.
L RobertDépartement d'oncologie médicale, Centre Eugène-Marquis, Rennes, France.
C Saavedra SerranoMedical Oncology Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.
M Gion CortésMedical Oncology Department, Hospital Universitario Ramón y Cajal, Madrid, Spain.
M Sampaio-AlvesFaculdade de Medicina, Universidade do Porto (FMUP), Oporto, Portugal.
M VitorinoOncology Department, Hospital Professor Doutor Fernando Fonseca, Amadora, Portugal.
L PecenInstitute of Computer Science, Czech Academy of Sciences, Praha, Czech Republic; Faculty of Medicine in Pilsen - Charles University, Pilsen, Czech Republic.
C SingerDepartment of Obstetrics and Gynecology and Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
N HarbeckBreast Center, Department of Gynecology and Obstetrics, Comprehensive Cancer Center of the Ludwig-Maximilians-University, Munich, Germany.
G RinnerthalerSalzburg Cancer Research Institute- Center for Clinical Cancer and Immunology Trials, Salzburg, Austria; Cancer Cluster Salzburg, Salzburg, Austria; IIIrd Medical Department with Haematology, Medical Oncology, Haemostaseology, Infectiology and Rheumatology, Oncologic Center, Paracelsus Medical University Salzburg, Salzburg, Austria.
R GreilSalzburg Cancer Research Institute- Center for Clinical Cancer and Immunology Trials, Salzburg, Austria; Cancer Cluster Salzburg, Salzburg, Austria; IIIrd Medical Department with Haematology, Medical Oncology, Haemostaseology, Infectiology and Rheumatology, Oncologic Center, Paracelsus Medical University Salzburg, Salzburg, Austria. Electronic address: r.greil@salk.at.
AGMT Study Group
Centre National de la Recherche Scientifique · FRHospital Universitario Ramón y Cajal · ESCentre Eugène Marquis · FRMedical University of Vienna · ATParacelsus Medical University · ATHospital Prof. Dr. Fernando Fonseca · PTOspedale Policlinico San Martino · ITCharles University · CZComprehensive Cancer Center Vienna · ATHospital Clínic de Barcelona · ESKrankenhaus der Elisabethinen · ATLKH Hochsteiermark · ATLudwig-Maximilians-Universität München · DEMarinha PortuguesaOspedale Santa Maria della Misericordia di Udine · ITThe Netherlands Cancer Institute · NLUniversidade do Porto · PTUniversity of Genoa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTriple-negative breast cancer (TNBC) is associated with poor prognosis, and new treatment options are urgently needed. About 34%-39% of primary TNBCs show a low expression of human epidermal growth factor receptor 2 (HER2-low), which is a target for new anti-HER2 drugs. However, little is known about the frequency and the prognostic value of HER2-low in metastatic TNBC. PATIENTS AND

methodsWe retrospectively included patients with TNBC from five European countries for this international, multicenter analysis. Triple-negativity had to be shown in a metastatic site or in the primary breast tumor diagnosed simultaneously or within 3 years before metastatic disease. HER2-low was defined as immunohistochemically (IHC) 1+ or 2+ without ERBB2 gene amplification. Survival probabilities were calculated by the Kaplan-Meier method, and multivariable hazard ratios (HRs) were estimated by Cox regression models.

resultsIn total, 691 patients, diagnosed between January 2006 and February 2021, were assessable. The incidence of HER2-low was 32.0% [95% confidence interval (CI) 28.5% to 35.5%], with similar proportions in metastases (n = 265; 29.8%) and primary tumors (n = 425; 33.4%; P = 0.324). The median overall survival (OS) in HER2-low and HER2-0 TNBC was 18.6 and 16.1 months, respectively (HR 1.00; 95% CI 0.83-1.19; P = 0.969). Similarly, in multivariable analysis, HER2-low had no significant impact on OS (HR 0.95; 95% CI 0.79-1.13; P = 0.545). No difference in prognosis was observed between HER2 IHC 0/1+ and IHC 2+ tumors (HR 0.89; 95% CI 0.69-1.17; P = 0.414).

conclusionsIn this large international dataset of metastatic TNBC, the frequency of HER2-low was 32.0%. Neither in univariable nor in multivariable analysis HER2-low showed any influence on OS.

Indexed as

Triple Negative Breast NeoplasmsEuropeHumansPrognosisRetrospective StudiesHER2-lowmetastaticOSprognosisreal-world datatriple-negative breast cancer

Identifiers

PMID36563519
PMCPMC10024122
OpenAlexW4312129650

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.