<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-17T03:49:27Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/12945" metadataPrefix="marc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/12945</identifier><datestamp>2025-05-03T03:19:58Z</datestamp><setSpec>com_2072_378070</setSpec><setSpec>com_2072_378040</setSpec><setSpec>col_2072_378092</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Tapia Céspedes, Marta</subfield>
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      <subfield code="a">Marín-Aguilera, Mercedes</subfield>
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      <subfield code="a">Hernández-Illán, Eva</subfield>
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      <subfield code="a">Tébar, C.</subfield>
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      <subfield code="a">Martínez-Puchol, Ana Isabel</subfield>
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      <subfield code="a">Martínez-Sáez, Olga</subfield>
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      <subfield code="a">Villacampa Javierre, Guillermo</subfield>
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      <subfield code="a">Rezqallah Arón , María Alejandra</subfield>
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      <subfield code="a">Saura Manich, Cristina</subfield>
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      <subfield code="a">Escriva de Romani, Santiago</subfield>
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      <subfield code="c">2025-04-11T12:39:46Z</subfield>
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      <subfield code="c">2025-04-11T12:39:46Z</subfield>
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      <subfield code="c">2025-06</subfield>
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      <subfield code="a">Early breast cancer; HER2 positive; Genomic test</subfield>
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      <subfield code="a">Càncer de mama precoç; HER2 positiu; Prova genòmica</subfield>
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      <subfield code="a">Cáncer de mama precoz; HER2 positivo; Prueba genómica</subfield>
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      <subfield code="a">Background&#xd;
HER2DX is a clinically available genomic assay that provides prognostic (relapse risk score), predictive [pathological complete response (pCR) likelihood score], and ERBB2 expression data in stage I-III human epidermal growth factor receptor 2 (HER2)-positive breast cancer (BC). This real-world study evaluated its clinical impact.&#xd;
Patients and methods&#xd;
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.&#xd;
Results&#xd;
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 (P &lt; 0.001). In 69 patients with pCR-high disease, less intensive treatment achieved similar pCR rates compared with multi-agent chemotherapy (81.5% versus 69.0%; odds ratio = 1.97, P = 0.256). Physician confidence improved (P &lt; 0.001) and the estimated total cost savings, including direct drug costs, vein access devices, and HER2DX costs, amounted to €98 031.&#xd;
Conclusions&#xd;
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.</subfield>
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      <subfield code="a">FS is supported by a Rio Hortega clinical scientist contract from the Instituto de Salud Carlos III (ISCIII) [grant number CM22/00073]. FBM received funding from Fundación científica AECC Ayudas Investigador AECC 2021 [grant number INVES21943BRAS].</subfield>
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      <subfield code="a">http://hdl.handle.net/11351/12945</subfield>
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      <subfield code="a">Cromosomes humans - Anomalies - Diagnòstic</subfield>
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      <subfield code="a">Mama - Càncer - Tractament</subfield>
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      <subfield code="a">DISEASES::Neoplasms::Neoplasms by Site::Breast Neoplasms</subfield>
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      <subfield code="a">ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de la mama</subfield>
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