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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorTapia Céspedes, Marta
dc.contributor.authorMarín-Aguilera, Mercedes
dc.contributor.authorHernández-Illán, Eva
dc.contributor.authorTébar, C.
dc.contributor.authorMartínez-Puchol, Ana Isabel
dc.contributor.authorMartínez-Sáez, Olga
dc.contributor.authorVillacampa Javierre, Guillermo
dc.contributor.authorRezqallah Arón , María Alejandra
dc.contributor.authorSaura Manich, Cristina
dc.contributor.authorEscriva de Romani, Santiago
dc.date.accessioned2025-04-11T12:39:46Z
dc.date.available2025-04-11T12:39:46Z
dc.date.issued2025-06
dc.identifier.citationMartínez-Sáez O, Tapia M, Marín-Aguilera M, Hernández-Illán E, Tébar C, Martinez-Puchol AI, et al. Clinical decision impact of HER2DX, an algorithm-powered genomic diagnostic in early-stage HER2-positive breast cancer: results from a prospective real-world study. ESMO Real World Data Digit Oncol. 2025 Jun;8:100123.
dc.identifier.issn2949-8201
dc.identifier.urihttp://hdl.handle.net/11351/12945
dc.descriptionCáncer de mama precoz; HER2 positivo; Prueba genómica
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesESMO Real World Data and Digital Oncology;8
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectCromosomes humans - Anomalies - Diagnòstic
dc.subjectMama - Càncer - Tractament
dc.subjectMama - Càncer - Diagnòstic
dc.subjectGenòmica
dc.subject.meshBreast Neoplasms
dc.subject.mesh/drug therapy
dc.subject.meshBreast Neoplasms
dc.subject.mesh/diagnosis
dc.subject.meshGenomics
dc.subject.meshGenetic Testing
dc.titleClinical decision impact of HER2DX, an algorithm-powered genomic diagnostic in early-stage HER2-positive breast cancer: results from a prospective real-world study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.esmorw.2025.100123
dc.subject.decsneoplasias de la mama
dc.subject.decs/farmacoterapia
dc.subject.decsneoplasias de la mama
dc.subject.decs/diagnóstico
dc.subject.decsgenómica
dc.subject.decspruebas genéticas
dc.relation.publishversionhttps://doi.org/10.1016/j.esmorw.2025.100123
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Martínez-Sáez O] Translational Genomics and Targeted Therapies in Solid Tumors, August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain. Department of Medical Oncology, Cancer Institute and Blood Disorders, Hospital Clinic of Barcelona, Barcelona, Spain. Department of Medicine, University of Barcelona, Barcelona, Spain. [Tapia M, Tébar C] Medical Oncology Department, Hospital Clínico Universitario de Valencia (INCLIVA), Valencia, Spain. [Marín-Aguilera M] Reveal Genomics, Barcelona, Spain. [Hernández-Illán E, Martinez-Puchol AI] Core Molecular Laboratory, Hospital Clinic of Barcelona, Barcelona, Spain. [Villacampa G] Statistics Unit, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [Rezqallah A, Escrivà S] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [Saura C] SOLTI Breast Cancer Cooperative Group, Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PEICTI2021-2023/CM22%2F00073
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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