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dc.contributor.authorMartín, Miguel
dc.contributor.authorPandiella Alonso, Atanasio 
dc.contributor.authorVargas-Castrillón, Emilio
dc.contributor.authorDíaz Rodríguez, María Elena 
dc.contributor.authorIglesias-Hernangómez, Teresa
dc.contributor.authorMartínez Cano, Concha
dc.contributor.authorFernández-Cuesta, Inés
dc.contributor.authorWinkow, Elena
dc.contributor.authorPerelló, Maria Francesca
dc.date.accessioned2025-11-11T12:49:21Z
dc.date.available2025-11-11T12:49:21Z
dc.date.issued2024-04-16
dc.identifier.citationMartín M, Pandiella A, Vargas-Castrillón E, Díaz-Rodríguez E, Iglesias-Hernangómez T, Martínez Cano C, Fernández-Cuesta I, Winkow E, Perelló MF. Trastuzumab deruxtecan in breast cancer. Crit Rev Oncol Hematol. 2024 Jun;198:104355. doi: 10.1016/j.critrevonc.2024.104355. Epub 2024 Apr 16. PMID: 38621469.es_ES
dc.identifier.issn1040-8428
dc.identifier.urihttp://hdl.handle.net/10366/167788
dc.description.abstract[EN]Trastuzumab deruxtecan (T-DXd) is an antibody-drug conjugate (ADC) consisting of a humanised, anti-human epidermal growth factor receptor 2 (HER2) monoclonal antibody covalently linked to a topoisomerase I inhibitor cytotoxic payload (DXd). The high drug-to-antibody ratio (8:1) ensures a high DXd concentration is delivered to target tumour cells, following internalisation of T-DXd and subsequent cleavage of its tetrapeptide-based linker. DXd's membrane-permeable nature enables it to cross cell membranes and potentially exert antitumour activity on surrounding tumour cells regardless of HER2 expression. T-DXd's unique mechanism of action is reflected in its efficacy in clinical trials in patients with HER2-positive advanced breast cancer (in heavily pretreated populations and in those previously treated with a taxane and trastuzumab), as well as HER2-low metastatic breast cancer. Thus, ADCs such as T-DXd have the potential to change the treatment paradigm of targeting HER2 in metastatic breast cancer, including eventually within the adjuvant/neoadjuvant setting.es_ES
dc.description.sponsorshipThis work was supported by Daiichi Sankyo and AstraZeneca. Both funding sources were involved in the writing of the manuscript.es_ES
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAntibody-drug conjugate; HER2-low metastatic breast cancer; HER2-positive metastatic breast cancer; Trastuzumab deruxtecanes_ES
dc.titleTrastuzumab deruxtecan in breast canceres_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/ 10.1016/J.CRITREVONC.2024.104355es_ES
dc.subject.unesco2302.06 Quimioterapiaes_ES
dc.identifier.doi10.1016/j.critrevonc.2024.104355
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.journal.titleCritical Reviews in Oncology/Hematologyes_ES
dc.volume.number198es_ES
dc.page.initial104355es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.description.projectThis work was supported by Daiichi Sankyo and AstraZeneca. Both funding sources were involved in the writing of the manuscriptes_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internacional