Second-line treatment options for patients with metastatic triple-negative breast cancer: a review of the clinical evidence

dc.contributor.author
García-Sáenz, José Ángel
dc.contributor.author
Rodríguez-Lescure, Álvaro
dc.contributor.author
Cruz, Josefina
dc.contributor.author
Albanell Mestres, Joan
dc.contributor.author
Alba, Emilio
dc.contributor.author
Llombart-Cussac, Antonio
dc.date.accessioned
2026-01-29T14:42:39Z
dc.date.available
2026-01-29T14:42:39Z
dc.date.issued
2026-01-28T16:11:59Z
dc.date.issued
2026-01-28T16:11:59Z
dc.date.issued
2025
dc.date.issued
2026-01-28T16:11:59Z
dc.identifier
Garcia-Saenz JA, Rodriguez-Lescure A, Cruz J, Albanell J, Alba E, Llombart A. Second-line treatment options for patients with metastatic triple-negative breast cancer: a review of the clinical evidence. Target Oncol. 2025;20(2):191-213. DOI: 10.1007/s11523-024-01125-1
dc.identifier
1776-2596
dc.identifier
https://hdl.handle.net/10230/72394
dc.identifier
http://dx.doi.org/10.1007/s11523-024-01125-1
dc.identifier.uri
http://hdl.handle.net/10230/72394
dc.description.abstract
Metastatic triple-negative breast cancer has a poor prognosis and poses significant therapeutic challenges. Until recently, limited therapeutic options have been available for patients with advanced disease after failure of first-line chemotherapy. The aim of this review is to assess the current evidence supporting second-line treatment options in patients with metastatic triple-negative breast cancer. Evidence was reviewed from controlled clinical trials in which eribulin, vinorelbine, capecitabine, gemcitabine, gemcitabine plus carboplatin, fam-trastuzumab-deruxtecan, sacituzumab govitecan, olaparib, and talazoparib were used in the second-line treatment for metastatic breast cancer, either as study drugs or as comparators. The benefit of treatment was evaluated using the European Society for Medical Oncology-Magnitude of Clinical Benefit Scale. Based on the evidence review, sacituzumab govitecan was identified as the preferred second-line treatment option for patients with metastatic triple-negative breast cancer, supported by clinical evidence and consensus across international clinical guidelines. Olaparib and talazoparib are of use in patients with human epidermal growth factor receptor 2-negative metastatic breast cancer and germline BRCA1/2 mutations. Exploratory data for fam-trastuzumab-deruxtecan suggest a survival benefit in human epidermal growth factor receptor 2-low, hormone-receptor-negative patients, but further solid evidence is required. Other chemotherapies with lower European Society for Medical Oncology-Magnitude of Clinical Benefit Scale scores may continue to be useful in highly selected patients.
dc.format
application/pdf
dc.format
application/pdf
dc.language
eng
dc.publisher
Springer
dc.relation
Targeted Oncology. 2025;20(2):191-213
dc.rights
© The Author(s) 2025, corrected publication 2025. Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.
dc.rights
http://creativecommons.org/licenses/by-nc/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.subject
Mama--Càncer
dc.title
Second-line treatment options for patients with metastatic triple-negative breast cancer: a review of the clinical evidence
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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