Evidence map›Paper›PMID 41647709›Full record

ArticleESMO real world data and digital oncology2025

Clinical decision impact of HER2DX, an algorithm-powered genomic diagnostic in early-stage HER2-positive breast cancer: results from a prospective real-world study.

O Martínez-Sáez, M Tapia, M Marín-Aguilera, E Hernández-Illán, C Tébar, A I Martinez-Puchol, P Jares, S Marín-Liébana, A Magro, J A Puig-Butille and 37 more

Abstract read
In one paragraph

Article in ESMO real world data and digital oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Trial
  2. Observational
  3. Article
  4. Article
  5. Associations of the HER2DX Genomic Test with Biological and Pathologic Features in HER2-Positive Breast Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  6. Article
  7. Article
  8. Review
  9. 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

47 authors.

O Martínez-SáezTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
M TapiaMedical Oncology Department, Hospital Clínico Universitario de Valencia (INCLIVA), Valencia, Spain.
M Marín-AguileraReveal Genomics, Barcelona, Spain.
E Hernández-IllánCore Molecular Laboratory, Hospital Clinic of Barcelona, Barcelona, Spain.
C TébarMedical Oncology Department, Hospital Clínico Universitario de Valencia (INCLIVA), Valencia, Spain.
A I Martinez-PucholCore Molecular Laboratory, Hospital Clinic of Barcelona, Barcelona, Spain.
P JaresPathology Department, Hospital Clínic of Barcelona, Barcelona, Spain.
S Marín-LiébanaMedical Oncology Department, Hospital Arnau de Vilanova, Valencia, Spain.
A MagroMedical Oncology Department, Hospital Comarcal Francesc de Borja, Gandia, Spain.
J A Puig-ButilleCore Molecular Laboratory, Hospital Clinic of Barcelona, Barcelona, Spain.
L PalomarMedical Oncology Department, Hospital de Sagunto, Sagunto, Spain.
E SanfeliuTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
M T MartinezMedical Oncology Department, Hospital Clínico Universitario de Valencia (INCLIVA), Valencia, Spain.
M V LosadaTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
C HernandoMedical Oncology Department, Hospital Clínico Universitario de Valencia (INCLIVA), Valencia, Spain.
B AdamoTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
V IranzoMedical Oncology Department, Hospital General Universitario de Valencia, Valencia, Spain.
T PascualTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
A PouptsisMedical Oncology Department, Hospital Universitario de la Ribera, Alzira, Spain.
F SchettiniTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
A SantaballaMedical Oncology Department, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
B ConteTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
M D TorregrosaMedical Oncology Department, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
F Brasó-MaristanyTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
B WalbaumTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
R Gómez-BravoTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
O BurguésMedical Oncology Department, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
I G FructuosoTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
I Garrido-CanoMedical Oncology Department, Hospital Clínico Universitario de Valencia (INCLIVA), Valencia, Spain.
E SeguíTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
L ParéReveal Genomics, Barcelona, Spain.
M MuñozTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
E CarceleroPharmacy Department, Hospital Clinic Barcelona, Barcelona, Spain.
J SànchezDepartment of Medical Oncology, Cancer Institute and Blood Disorders, Hospital Clinic of Barcelona, Barcelona, Spain.
P Villagrasa-GonzálezReveal Genomics, Barcelona, Spain.
W BuckinghamReveal Genomics, Barcelona, Spain.
A PratTranslational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain.
G VillacampaStatistics Unit, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
N ChicMedical Oncology Department, Peter MacCallum Cancer Centre, Melbourne, Australia.
P RiveraDepartment of Medical Oncology, Cancer Institute and Blood Disorders, Hospital Clinic of Barcelona, Barcelona, Spain.
A RezqallahVall d'Hebron University Hospital, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
C SauraSOLTI Breast Cancer Cooperative Group, Barcelona, Spain.
S EscrivàVall d'Hebron University Hospital, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.
B BermejoMedical Oncology Department, Hospital Clínico Universitario de Valencia (INCLIVA), Valencia, Spain.
A LluchMedical Oncology Department, Hospital Clínico Universitario de Valencia (INCLIVA), Valencia, Spain.
A LlombartMedical Oncology Department, Hospital Arnau de Vilanova, Valencia, Spain.
J M CejalvoMedical Oncology Department, Hospital Clínico Universitario de Valencia (INCLIVA), Valencia, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: HER2DX is a clinically available genomic assay that provides prognostic (relapse risk score), predictive [pathological complete response (pCR) likelihood score], and Patients and methods: This prospective study enrolled newly diagnosed patients with stage I-III HER2-positive BC across 12 hospitals in Spain (November 2021-September 2024). Thirty-four oncologists ordered HER2DX and completed questionnaires before and after receiving results to assess treatment changes (primary objective). Secondary objectives included evaluating the HER2DX pCR likelihood score association with pCR, test turnaround time, changes in physician confidence regarding treatment decisions, and cost-effectiveness. Results: Among 297 recruited patients, 48.1% (95% confidence interval 42.5% to 53.7%) experienced treatment adjustments after HER2DX. Within these cases, 73.5% involved reduced treatment intensity, 24.5% involved increased treatment intensity, and the remaining cases (2.0%) involved mixed adjustments. Of the cases with reduced treatment intensity, 56.2% had a reduction in chemotherapy intensity, 26.7% had a reduction in anti-HER2 therapy, and 17.1% in both. Among the 182 patients with available pathological data at surgery, the pCR likelihood score was a significant predictor of pCR ( Conclusions: HER2DX impacts clinical management in stage I-III HER2-positive BC by supporting treatment adjustments, enhancing physician confidence, maintaining pCR rates, and reducing health care costs.

Indexed as

early breast cancergenomic testhealth economicsHER2DXHER2 positive

Identifiers

PMID41647709
PMCPMC12836513

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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.