<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-28T20:34:22Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/118832" metadataPrefix="marc">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/118832</identifier><datestamp>2025-03-18T13:29:21Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Santander Ballestín, Sonia</subfield>
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      <subfield code="a">Abadía Labena, María</subfield>
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      <subfield code="a">Avedillo-Salas, Ana</subfield>
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      <subfield code="a">Marco Continente, Cristina</subfield>
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      <subfield code="a">Arribas Blázquez, Marina</subfield>
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      <subfield code="a">Luesma Bartolomé, María José</subfield>
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      <subfield code="c">2025-02-24</subfield>
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      <subfield code="a">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.</subfield>
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      <subfield code="a">Simple Summary:
Breast cancer is the most common malignant neoplasm worldwide and the most prevalent one among women. Cyclin-dependent kinase 4 and 6 inhibitors have become a novel form 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. These inhibitors are considered a new standard treatment for this pathology, offering lower toxicity than chemotherapy.</subfield>
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      <subfield code="a">Santander Ballestín, S.; Abadía Labena, M.; Avedillo-Salas, A.; Marco Continente, C.; Arribas Blázquez, M.; Luesma Bartolomé, M.J. Advances in CDK4 and 6 Inhibitors: Transforming Breast Cancer Treatment. Cancers 2025, 17, 760. https://doi.org/10.3390/cancers17050760</subfield>
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      <subfield code="a">2072-6694</subfield>
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      <subfield code="a">10.3390/cancers17050760</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.14352/118832</subfield>
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      <subfield code="a">https://doi.org/10.3390/cancers17050760</subfield>
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      <subfield code="a">40075608</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Advances in CDK4 and 6 Inhibitors: Transforming Breast Cancer Treatment.</subfield>
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