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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.3390/cancers17050760</dc:identifier><dc:language>eng</dc:language><dc:creator>Santander Ballestín, Sonia</dc:creator><dc:creator>Abadía Labena, María</dc:creator><dc:creator>Avedillo-Salas, Ana</dc:creator><dc:creator>Marco Continente, Cristina</dc:creator><dc:creator>Arribas Blázquez, Marina</dc:creator><dc:creator>Luesma Bartolomé, María José</dc:creator><dc:title>Advances in CDK4 and 6 inhibitors: transforming breast cancer treatment</dc:title><dc:identifier>ART-2025-143563</dc:identifier><dc:description>Background and Objectives: Breast cancer is the most common malignant neoplasm worldwide and the most prevalent one among women. It represents the leading cause of cancer-related death among females. Cyclin-dependent kinase 4 and 6 inhibitors disrupt the cell cycle, inducing cellular senescence and, ultimately, apoptosis. Consequently, they have become a novel type of adjuvant therapy for the treatment of advanced or metastatic breast cancer characterised by positive hormone receptors and human epidermal growth factor receptor 2 (HER-2) negative. Methods: A systematic review was conducted, analysing the available literature on cyclin-dependent kinase 4 and 6 inhibitors published over the last five years. The aim was to evaluate the efficacy and safety of adding these drugs to the standard endocrine therapy for this pathology. Results: The combination of cyclin-dependent kinase 4 and 6 inhibitors with endocrine therapy was shown to improve progression-free survival, overall survival, and chemotherapy-free intervals in patients who received this combination therapy. Conclusions: The addition of CDK4/6 inhibitors to endocrine therapy in the treatment of advanced or metastatic breast cancer with positive hormone receptors and HER-2 negative significantly improved PFS, median survival, and chemotherapy-free intervals compared with the use of hormonal treatments alone or in combination with a placebo. Currently, CDK4/6 inhibitors are becoming established as a new standard treatment for this pathology, offering lower toxicity than chemotherapy. However, it is necessary to deeply investigate the mechanisms of treatment resistance and develop effective therapies to overcome them.</dc:description><dc:date>2025</dc:date><dc:source>http://zaguan.unizar.es/record/153135</dc:source><dc:doi>10.3390/cancers17050760</dc:doi><dc:identifier>http://zaguan.unizar.es/record/153135</dc:identifier><dc:identifier>oai:zaguan.unizar.es:153135</dc:identifier><dc:identifier.citation>Cancers 17, 5 (2025), 760 [20 pp.]</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>https://creativecommons.org/licenses/by/4.0/deed.es</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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