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dc.contributor.authorGonzález Conde, Miriam
dc.contributor.authorYáñez Gómez, Celso
dc.contributor.authorLópez López, Rafael 
dc.contributor.authorCosta Nogueira, Clotilde
dc.date.accessioned2023-03-03T08:35:55Z
dc.date.available2023-03-03T08:35:55Z
dc.date.issued2021
dc.identifier.issn2075-4426
dc.identifier.urihttp://hdl.handle.net/20.500.11940/17389
dc.description.abstractBreast cancer (BC) is the most common cancer diagnosed in women worldwide. Approximately 70% of BC patients have the luminal subtype, which expresses hormone receptors (HR+). Adjuvant endocrine treatments are the standard of care for HR+/HER2- BC patients. Over time, approximately 30% of those patients develop endocrine resistance and metastatic disease. Cyclin-dependent kinase inhibitors (CDKi), in combination with an aromatase inhibitor or fulvestrant, have demonstrated superior efficacies in increasing progression-free survival, with a safe toxicity profile, in HR+/HER2- metastatic BC patients. CDKi blocks kinases 4/6, preventing G1/S cell cycle transition. However, not all of the patients respond to CDKi, and those who do respond ultimately develop resistance to the combined therapy. Studies in tumour tissues and cell lines have tried to elucidate the mechanisms that underlie this progression, but there are still no conclusive data. Over the last few years, liquid biopsy has contributed relevant information. Circulating tumour materials are potential prognostic markers for determining patient prognosis in metastatic luminal BC, for monitoring disease, and for treatment selection. This review outlines the different studies performed using liquid biopsy in patients with HR+ metastatic BC treated with CDKi plus endocrine therapy. We mainly focus on those studies that describe the possible resistance mechanisms in circulating tumour-derived material.
dc.language.isoenes
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleLiquid Biopsy: A New Tool for Overcoming CDKi Resistance Mechanisms in Luminal Metastatic Breast Cancer
dc.typeJournal Articlees
dc.authorsophosGonzalez-Conde, M.;Yanez-Gomez, C.;Lopez-Lopez, R.;Costa, C.
dc.identifier.doi10.3390/jpm11050407
dc.identifier.sophos44697
dc.issue.number5
dc.journal.titleJOURNAL OF PERSONALIZED MEDICINE
dc.organizationÁrea Sanitaria de Santiago de Compostela e Barbanza
dc.organizationSERGAS
dc.rights.accessRightsopenAccess
dc.typesophosArtículo de Revisiónes
dc.volume.number11


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