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Validation of the HER2DX genomic test in first-line advanced HER2-positive breast cancer treated with trastuzumab, pertuzumab, and taxane

  • Marcin Kubeczko
  • , Sandra Cobo
  • , Rodrigo Sanchez-Bayona
  • , Bartłomiej Pyciński
  • , Jesús Soberino
  • , Ewa Chmielik
  • , Esther Sanfeliu
  • , Maria Rey
  • , Francisco Pardo
  • , Angela Aguirre
  • , Oleguer Castillo
  • , Aleksandra Lesniak
  • , Malgorzata Oczko-Wojciechowska
  • , Esther Carcelero
  • , Barbara Adamo
  • , Maria Vidal
  • , Milana Bergamino
  • , Julia Maues
  • , Guillermo Villacampa
  • , Laia Paré
  • Patricia Villagrasa, Eva Ciruelos, Aleix Prat, Michal Jarzab, Fara Brasó-Maristany
  • Breast Cancer Center
  • Maria Sklodowska-Curie Institute of Oncology
  • Translational Genomics and Targeted Therapeutics in Solid Tumors
  • August Pi i Sunyer Biomedical Research Institute
  • Medical Oncology Department
  • Hospital Universitario 12 de Octubre
  • Breast Cancer Unit
  • Tumor Pathology Department
  • Pathology Department
  • Hospital Clinic of Barcelona
  • Department of Medicine
  • University of Barcelona
  • Reveal Genomics, S.L.
  • Genetic and Molecular Diagnostics of Cancer Department
  • Pharmacy Department
  • Clínic Barcelona Comprehensive Cancer Center
  • GRASP
  • Statistics Unit
  • Vall d'Hebron Institute of Oncology

Research output: Contribution to journalArticlepeer-review

Abstract

Trastuzumab, pertuzumab, and a taxane (THP) has been the standard first-line therapy for HER2+ advanced breast cancer for over a decade. With new regimens emerging, genomic tools like HER2DX may help identify patients who benefit durably from THP versus those requiring intensification. Here, baseline tumor tissue from 122 patients with HER2+ treated with THP in Poland was tested with HER2DX. A previously published Spanish real-world cohort (n = 93) was added to generate a combined cohort (n = 215). Univariable analyses were performed in the Polish cohort, and multivariable Cox and logistic regression models were applied to the combined cohort. A HER2DX metastatic prognostic score was trained on overall survival (OS) in the Spanish cohort and validated in the Polish cohort. In the Polish cohort, high ERBB2 mRNA scores were associated with significantly longer real-world progression-free survival (rwPFS) (33.8 vs. 17.9 months; hazard ratio [HR] 0.57; p = 0.022) and real-world overall survival (rwOS) (75.1 vs. 40.2; HR 0.48; p = 0.009). In the combined cohort, ERBB2 high-score tumors showed prolonged rwPFS (33.8 vs. 12.5; HR 0.50; p < 0.001) and rwOS (not reached vs. 37.1; HR 0.36; p < 0.001), and higher rwORR (84.4% vs. 52.0%; p < 0.001). Prognostic value was independent of clinical variables, including number of metastatic sites. Subgroup analyses showed particularly favorable outcomes in patients with <3 sites (median rwPFS 51.7 vs. 20.3 months). The HER2DX metastatic prognostic score outperformed ERBB2 alone in the validation cohort. In conclusion, the HER2DX ERBB2 mRNA score provides independent prognostic information in HER2+ advanced breast cancer treated with THP. The HER2DX metastatic prognostic score further improves prognostic accuracy.

Original languageEnglish
Article number43
Journalnpj Breast Cancer
Volume12
Issue number1
DOIs
Publication statusPublished - Dec 2026

ASJC Scopus subject areas

  • Oncology
  • Radiology, Nuclear Medicine and Imaging
  • Pharmacology (medical)

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