HER2DX ERBB2 mRNA expression in advanced HER2- positive breast cancer treated with T-DM1
| dc.contributor.author | Brasó Maristany, Fara | |
| dc.contributor.author | Griguolo, Gaia | |
| dc.contributor.author | Chic Ruché, Núria | |
| dc.contributor.author | Pascual, Tomás | |
| dc.contributor.author | Paré Brunet, Laia | |
| dc.contributor.author | Maues, Julia | |
| dc.contributor.author | Galván, Patricia | |
| dc.contributor.author | Dieci, Maria Vittoria | |
| dc.contributor.author | Miglietta, Federica | |
| dc.contributor.author | Giarratano, Tommaso | |
| dc.contributor.author | Martínez Sáez, Olga | |
| dc.contributor.author | Marín Aguilera, Mercedes | |
| dc.contributor.author | Schettini, Francesco | |
| dc.contributor.author | Conte, Benedetta | |
| dc.contributor.author | Angelats, Laura | |
| dc.contributor.author | Vidal Losada, Maria Jesús | |
| dc.contributor.author | Adamo, Barbara | |
| dc.contributor.author | Muñoz, Montse | |
| dc.contributor.author | Sanfeliu, Esther | |
| dc.contributor.author | González Farré, Blanca | |
| dc.contributor.author | Vivancos, Ana | |
| dc.contributor.author | Villagrasa, Patricia | |
| dc.contributor.author | Parker, Joel S. | |
| dc.contributor.author | Perou, Charles M. | |
| dc.contributor.author | Conte, Pierfranco | |
| dc.contributor.author | Prat Aparicio, Aleix | |
| dc.contributor.author | Guarneri, Valentina | |
| dc.date.accessioned | 2023-03-01T14:10:05Z | |
| dc.date.available | 2023-12-31T06:10:21Z | |
| dc.date.issued | 2022-12 | |
| dc.date.updated | 2023-03-01T14:10:05Z | |
| dc.description.abstract | In advanced HER2-positive (HER2+) breast cancer (BC), the new antibody-drug conjugate trastuzumab deruxtecan (T-DXd) is more effective compared to trastuzumab emtansine (T-DM1). However, T-DXd can have significant toxicities, and the right treatment sequence is unknown. Biomarkers to guide the use of anti-HER2 therapies beyond HER2 status are needed. Here, we evaluated if pre-established levels of ERBB2 mRNA expression according to the HER2DX standardized assay are associated with response and survival following T-DM1. In ERBB2 low, medium, and high groups, the overall response rate was 0%, 29% and 56%, respectively (P<.001). ERBB2 mRNA was significantly associated with better progression-free survival (p = 0.002) and overall survival (OS; P = 0.02). These findings were independent of HER2 IHC levels, hormone receptor, age, brain metastasis and line of therapy. The HER2DX risk-score (P=.04) and the immunoglobulin (IGG) signature (P=.04) were significantly associated with OS since diagnosis. HER2DX provides prognostic and predictive information following T-DM1 in advanced HER2+ BC. | |
| dc.format.extent | 14 p. | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.idgrec | 731692 | |
| dc.identifier.issn | 0027-8874 | |
| dc.identifier.pmid | 36576009 | |
| dc.identifier.uri | https://hdl.handle.net/2445/194390 | |
| dc.language.iso | eng | |
| dc.publisher | Oxford University Press | |
| dc.relation.isformatof | Versió postprint del document publicat a: https://doi.org/10.1093/jnci/djac227 | |
| dc.relation.ispartof | JNCI: Journal of The National Cancer Institute, 2022 | |
| dc.relation.uri | https://doi.org/10.1093/jnci/djac227 | |
| dc.rights | (c) Brasó Maristany, Fara et al., 2022 | |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | |
| dc.source | Articles publicats en revistes (Medicina) | |
| dc.subject.classification | Tumors cerebrals | |
| dc.subject.classification | Metàstasi | |
| dc.subject.classification | Càncer de mama | |
| dc.subject.classification | Expressió gènica | |
| dc.subject.classification | Cèl·lules T | |
| dc.subject.other | Brain tumors | |
| dc.subject.other | Metastasis | |
| dc.subject.other | Breast cancer | |
| dc.subject.other | Gene expression | |
| dc.subject.other | T cells | |
| dc.title | HER2DX ERBB2 mRNA expression in advanced HER2- positive breast cancer treated with T-DM1 | |
| dc.type | info:eu-repo/semantics/article | |
| dc.type | info:eu-repo/semantics/acceptedVersion |
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