Evidence map›Paper›PMID 40754555›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2026

Prognostic value of circulating HER2 extracellular domain in patients with HER2-positive metastatic breast carcinoma treated with TDM-1 (trastuzumab emtansine).

Roman Vion, Céline Calbrix, Anca Berghian, Emilie Lévêque, Maxime Fontanilles, Cédric Paquin, Philippe Ruminy, Jean Rouvet, Marianne Leheurteur, Nathalie Olympios and 3 more

Abstract read
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In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2026. 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. Review
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

13 authors.

Roman VionMedical Oncology Department, Centre Henri Becquerel, 1 Rue d'Amiens, 76038, Rouen, France. roman.vion@chb.unicancer.fr.ORCID http://orcid.org/0000-0003-2244-8650
Céline CalbrixBiology Department, Centre Henri Becquerel, Rouen, France.
Anca BerghianAnatomic Pathology Department, Centre Henri Becquerel, Rouen, France.
Emilie LévêqueClinical Research Unit, Centre Henri Becquerel, Rouen, France.
Maxime FontanillesMedical Oncology Department, Centre Henri Becquerel, 1 Rue d'Amiens, 76038, Rouen, France.
Cédric PaquinBiology Department, Centre Henri Becquerel, Rouen, France.
Philippe RuminyUniversity of Rouen Normandie, Inserm U1245, Rouen, France.
Jean RouvetPharmacy Department, Centre Henri Becquerel, Rouen, France.
Marianne LeheurteurMedical Oncology Department, Centre Henri Becquerel, 1 Rue d'Amiens, 76038, Rouen, France.
Nathalie OlympiosMedical Oncology Department, Centre Henri Becquerel, 1 Rue d'Amiens, 76038, Rouen, France.
Vinciane RainvilleUniversity of Rouen Normandie, Inserm U1245, Rouen, France.
Frédéric Di FioreMedical Oncology Department, Centre Henri Becquerel, 1 Rue d'Amiens, 76038, Rouen, France.
Florian ClatotMedical Oncology Department, Centre Henri Becquerel, 1 Rue d'Amiens, 76038, Rouen, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAntibody-drug conjugates (ADC) improved survival in patients with HER2-positive MBC. To date, there is  no prognostic biomarker in routine practice for these patients. HER2-ECD is associated with poor prognosis but has not yet been studied in patients receiving ADC.

methodsThis monocentric retrospective study assessed in HER2-positive MBC patients shows the prognostic value on OS and PFS of (1) baseline HER2-ECD and CA15-3 and (2) HER2-ECD and CA15-3 after 3 months of treatment with TDM-1. At baseline, patients were divided according to the median value of HER2-ECD and CA15-3 from study population. For kinetic assessments, we compared survival outcomes according to the evolution of HER2-ECD and CA15-3 (stable/decrease vs increase).

results40 patients were included. For both biomarkers, baseline values were not prognostic for OS neither PFS. Patients with stable or decrease HER2-ECD at 3 months had a significantly longer OS (median 43 versus 15.3 months, p < 0.0001) and PFS (median 9.4 versus 2.9 months, p = 0.0018) than patients with decrease, confirmed in multivariate analysis (p = 0.004 for OS and < 0.0001 for PFS). In contrast, CA15-3 kinetic was only prognostic for PFS (median 9.6 versus 4.9 months, p = 0.019), confirmed in multivariate analysis (p = 0.008).

conclusionIn this retrospective cohort, HER2-ECD kinetic was a prognostic biomarker for OS and PFS in patients with an HER2-positive MBC treated with TDM-1.

Indexed as

Ado-Trastuzumab EmtansineAntineoplastic Agents, ImmunologicalBiomarkers, TumorBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesAdultAgedAged, 80 and overFemaleHumansMiddle AgedMucin-1PrognosisRetrospective StudiesAdo-Trastuzumab EmtansineAntineoplastic Agents, ImmunologicalBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesMucin-1Antibody–drug conjugateBreast cancerHER2 extracellular domainHER2-positivePrognosisTrastuzumab emtansin

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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.