Evidence map›Paper›PMID 40913834›Full record

ArticleESMO open2025

HER2DX ERBB2 score in advanced HER2-positive gastric cancer treated with trastuzumab and chemotherapy.

D Pesántez, F Brasó-Maristany, T Pascual, L Angelats, A Indacochea, M Cuatrecasas, S López, E Sanfeliu, G Fernández-Esparrach, L Notario and 6 more

Abstract read
In one paragraph

Article in ESMO open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

16 authors.

D PesántezDepartment of Medical Oncology, Hospital Clínic Barcelona, Barcelona, Spain; Translational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; Faculty of Medicine, University of Barcelona, Barcelona, Spain.
F Brasó-MaristanyTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; Reveal Genomics, Barcelona, Spain; Clínic Barcelona Comprehensive Cancer Center, Barcelona, Spain.
T PascualDepartment of Medical Oncology, Hospital Clínic Barcelona, Barcelona, Spain; Translational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; Faculty of Medicine, University of Barcelona, Barcelona, Spain; Clínic Barcelona Comprehensive Cancer Center, Barcelona, Spain.
L AngelatsDepartment of Medical Oncology, Hospital Clínic Barcelona, Barcelona, Spain; Translational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; Clínic Barcelona Comprehensive Cancer Center, Barcelona, Spain.
A IndacocheaDepartment of Medical Oncology, Hospital Clínic Barcelona, Barcelona, Spain; Translational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; Clínic Barcelona Comprehensive Cancer Center, Barcelona, Spain.
M CuatrecasasFaculty of Medicine, University of Barcelona, Barcelona, Spain; Clínic Barcelona Comprehensive Cancer Center, Barcelona, Spain; Pathology Department, Hospital Clinic Barcelona, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Madrid, Spain.
S LópezFaculty of Medicine, University of Barcelona, Barcelona, Spain; Pathology Department, Hospital Clinic Barcelona, Barcelona, Spain.
E SanfeliuDepartment of Medical Oncology, Hospital Clínic Barcelona, Barcelona, Spain; Translational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; Pathology Department, Hospital Clinic Barcelona, Barcelona, Spain.
G Fernández-EsparrachFaculty of Medicine, University of Barcelona, Barcelona, Spain; Clínic Barcelona Comprehensive Cancer Center, Barcelona, Spain; Endoscopy Unit, Department of Gastroenterology, IDIBAPS, CIBEREHD, Hospital Clínic Barcelona, Barcelona, Spain.
L NotarioDepartment of Medical Oncology, Hospital of Granollers, Granollers, Spain.
I MéndezDepartment of Pathology, Hospital of Granollers, Granollers, Spain.
D MomblanClínic Barcelona Comprehensive Cancer Center, Barcelona, Spain; Department of Gastrointestinal Surgery, Hospital Clínic Barcelona, Barcelona, Spain.
L CandiaDepartment of Medical Oncology, Hospital Clínic Barcelona, Barcelona, Spain; Translational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; Clínic Barcelona Comprehensive Cancer Center, Barcelona, Spain.
I MaciasDepartment of Medical Oncology, Hospital Clínic Barcelona, Barcelona, Spain; Translational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; Clínic Barcelona Comprehensive Cancer Center, Barcelona, Spain.
A PratDepartment of Medical Oncology, Hospital Clínic Barcelona, Barcelona, Spain; Translational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; Faculty of Medicine, University of Barcelona, Barcelona, Spain; Reveal Genomics, Barcelona, Spain; Clínic Barcelona Comprehensive Cancer Center, Barcelona, Spain. Electronic address: alprat@clinic.cat.
T SauriDepartment of Medical Oncology, Hospital Clínic Barcelona, Barcelona, Spain; Translational Genomics and Targeted Therapies in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; Faculty of Medicine, University of Barcelona, Barcelona, Spain; Clínic Barcelona Comprehensive Cancer Center, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundResponse to trastuzumab combined with chemotherapy (T-chemo) in human epidermal growth factor receptor 2 (HER2)-positive advanced gastric cancer (AGC) varies widely, highlighting the need for more precise biomarkers beyond conventional HER2 assessment with immunohistochemistry (IHC) and in situ hybridization (ISH). The HER2DX ERBB2 messenger RNA (mRNA) assay, a clinically validated genomic test initially developed for early-stage HER2-positive breast cancer, quantitatively measures ERBB2 expression and may improve patient selection for T-chemo in AGC. PATIENTS AND

methodsIn a retrospective cohort of 134 patients with AGC, including 58 who received T-chemo, we evaluated whether the HER2DX ERBB2 score defines more accurately HER2 status and correlates with treatment response and survival outcomes in HER2-positive AGC, compared with standard pathology-based methods.

resultsOur findings demonstrate that a high HER2DX ERBB2 score was significantly associated with improved progression-free survival [hazard ratio (HR) 0.81, 95% confidence interval (CI) 0.69-0.95, P = 0.012] and overall survival (HR 0.43, 95% CI 0.23-0.81, P = 0.008).

conclusionsThese results suggest that ERBB2 mRNA expression, as measured by HER2DX, may help refine selection for T-chemo and guide more personalized treatment strategies in HER2-positive AGC.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsErb-b2 Receptor Tyrosine KinasesStomach NeoplasmsTrastuzumabAdultAgedAntineoplastic Agents, ImmunologicalBiomarkers, TumorFemaleHumansMaleMiddle AgedRetrospective StudiesAntineoplastic Agents, ImmunologicalBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesTrastuzumabERBB2gastric cancergenomicsHER2DXHER2-positive

Identifiers

PMID40913834
PMCPMC12451336

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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.