Evidence map›Paper›PMID 42880095›Full record

ArticleBreast (Edinburgh, Scotland)2026

Clinical features associated with exceptional response on first-line anti-HER2-based therapy for metastatic breast cancer: real-world data from the ESME national cohort.

Thomas Grinda, Matthieu Carton, Stefania Morganti, Audrey Mailliez, Christelle Levy, Thierry Petit, Thomas Bachelot, Monica Arnedos, Véronique Diéras, Vincent Massard and 10 more

Abstract read
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In one paragraph

Article in Breast (Edinburgh, Scotland), 2026. 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
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.

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

20 authors.

Thomas GrindaMedical Oncology Department, Institut Gustave Roussy, Villejuif, France; Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA. Electronic address: thomas.grinda@gustaveroussy.fr.
Matthieu CartonDepartment of Biostatistics, Institut Curie, Saint-Cloud, France.
Stefania MorgantiDana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA.
Audrey MailliezMedical Oncology Department, Centre Oscar Lambret, Lille, France.
Christelle LevyMedical Oncology Department, Centre Francois Baclesse, Caen, France.
Thierry PetitMedical Oncology Department, Institut de Cancérologie Strasbourg Europe ICANS, Strasbourg, France.
Thomas BachelotMedical Oncology Department, Centre Léon Bérard, Lyon, France.
Monica ArnedosMedical Oncology Department, Institute Bergonié, Bordeaux, France.
Véronique DiérasMedical Oncology Department, Centre Eugene Marquis, Rennes, France.
Vincent MassardMedical Oncology Department, Institut de cancérologie de Lorraine, Vandoeuvre Les Nancy, France.
Florence DalencMedical Oncology Department, Oncopole Claudius Regaud, IUCT, Toulouse, France.
Isabelle DesmoulinsMedical Oncology Department, Centre Georges François Leclerc, Dijon, France.
Jean-Yves PiergaDepartment of Medical Oncology, Institut Curie, Paris, France.
Anthony GonçalvesMedical Oncology Department, Institut Paoli Calmettes, Marseille, France.
Caroline BailleuxMedical Oncology Department, Centre Antoine Lacassagne, Nice, France.
Jean-Sebastien FrenelMedical Oncology Department, Institut de Cancerologie de l'Ouest René Gauducheau, Saint-Herblain, France.
Lise BosquetHealth Data and Partnerships Department, Unicancer, Paris, France.
Heather A ParsonsDana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA.
William JacotMedical Oncology Department, Institut du cancer de Montpellier, INSERM U1194, Montpellier University, Montpellier, France.
Nancy U LinDana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some patients with HER2-positive metastatic breast cancer (MBC) achieve prolonged disease control with first-line anti-HER2-based therapy, but associated clinical features remain poorly characterized in real-world populations. We conducted a retrospective study using the Epidemiological Strategy and Medical Economics (ESME) MBC cohort, including 18 French comprehensive cancer centers. Women with HER2-positive MBC who initiated first-line anti-HER2-based therapy between January 2008 and December 2021 and had at least 3 years of follow-up were eligible. Exceptional responders had no documented progression within 3 years. A secondary analysis evaluated factors associated with remaining progression-free at 5 years. Multivariable logistic regression with bootstrap cross-validation was used. Among 4307 eligible patients, 1016 (23.6%) were exceptional responders. Of 765 evaluable at 5 years, 523 (68.4%) remained progression-free. Factors associated with a lower likelihood of exceptional response included hormone receptor-negative (HR-) disease, a disease-free interval of 6-24 months, ≥3 metastatic sites, visceral metastases, and central nervous system involvement. First-line treatment with chemotherapy, trastuzumab, and pertuzumab was associated with exceptional response. Among exceptional responders, HR-disease, grade III tumors and first-line chemotherapy plus trastuzumab and pertuzumab were associated with progression-free at 5-year, whereas visceral metastases were associated with lower odds. Model discrimination was moderate (AUC 0.72 and 0.64, respectively). Nearly one quarter of patients remained progression-free for at least 3 years, and more than two thirds of those evaluable remained progression-free at 5 years. Clinical variables alone had limited predictive value, supporting the need for molecular and immune biomarkers to better identify this subgroup.

Indexed as

HER2Metastatic breast cancerRWD exceptional responder

Identifiers

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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.