Pascual, TomásGonzález Farré, BlancaTeixidó Febrero, CristinaOleaga Zufiría, LauraOses, GabrielaGanau, SergiChic Ruché, NúriaRiu Viladoms, GiselaAdamo, BarbaraGalván, PatriciaVidal Losada, Maria JesúsSoy Muner, DolorsUrbano Ispizua, ÁlvaroMuñoz Mateu, MontserratPrat Aparicio, Aleix2021-06-172021-06-172019-06-070732-183Xhttps://hdl.handle.net/2445/178486Breast cancer is a biologically and clinically heterogeneous disease, and patients with similar clinical stage have markedly different outcomes. Triple-negative breast cancer (TNBC) is defined by the lack of expression of estrogen receptor (ER), progesterone receptor, and human epidermal growth factor receptor 2 (HER2).1,2 This subtype represents 15% to 20% of all breast cancers and is associated with the worst outcome of all subtypes, with greater tendency to distant recurrence in general and visceral metastasis in particular, including brain metastasis.3,4 To date, chemotherapy remains the standard of care for TNBCapplication/pdfeng(c) American Society of Clinical Oncology, 2019Càncer de mamaReceptors d'hormonesExpressió gènicaBreast cancerHormone receptorsGene expressionSignificant Clinical Activity of Olaparib in a Somatic BRCA1-Mutated Triple-Negative Breast Cancer With Brain Metastasisinfo:eu-repo/semantics/article6980282021-06-17info:eu-repo/semantics/openAccess