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   <dc:title>Camizestrant in Combination with Three Globally Approved CDK4/6 Inhibitors in Women with ER+, HER2- Advanced Breast Cancer: Results from SERENA-1</dc:title>
   <dc:creator>Ruiz , Manuel</dc:creator>
   <dc:creator>Vaklavas, Christos</dc:creator>
   <dc:creator>Baird, Richard</dc:creator>
   <dc:creator>BERMEJO, BEGOÑA</dc:creator>
   <dc:creator>Moreno, Irene</dc:creator>
   <dc:creator>Oliveira, Mafalda</dc:creator>
   <dc:subject>Medicaments antineoplàstics - Ús terapèutic</dc:subject>
   <dc:subject>Quimioteràpia combinada</dc:subject>
   <dc:subject>Proteïnes quinases - Inhibidors - Ús terapèutic</dc:subject>
   <dc:subject>Posologia</dc:subject>
   <dc:subject>DISEASES::Neoplasms::Neoplasms by Site::Breast Neoplasms</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::Other subheadings::/drug therapy</dc:subject>
   <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Therapeutics::Drug Therapy::Antineoplastic Protocols::Therapeutics::Drug Therapy::Antineoplastic Combined Chemotherapy Protocols</dc:subject>
   <dc:subject>CHEMICALS AND DRUGS::Chemical Actions and Uses::Pharmacologic Actions::Molecular Mechanisms of Pharmacological Action::Enzyme Inhibitors::Protein Kinase Inhibitors</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::Other subheadings::/administration &amp; dosage</dc:subject>
   <dc:subject>ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de la mama</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia</dc:subject>
   <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::terapéutica::farmacoterapia::protocolos antineoplásicos::terapéutica::farmacoterapia::protocolos de quimioterapia antineoplásica combinada</dc:subject>
   <dc:subject>COMPUESTOS QUÍMICOS Y DROGAS::acciones y usos químicos::acciones farmacológicas::mecanismos moleculares de acción farmacológica::inhibidores enzimáticos::inhibidores de proteínas cinasas</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/administración &amp; dosificación</dc:subject>
   <dcterms:abstract>Camizestrant; CDK4/6 inhibitors; Advanced breast cancer</dcterms:abstract>
   <dcterms:abstract>Camizestrant; Inhibidors de CDK4/6; Càncer de mama avançat</dcterms:abstract>
   <dcterms:abstract>Camizestrant; Inhibidores de CDK4/6; Cáncer de mama avanzado</dcterms:abstract>
   <dcterms:abstract>Purpose: This trial investigated the safety and tolerability of camizestrant with cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) in women with estrogen receptor-positive, HER2- advanced breast cancer.&#xd;
Patients and methods: SERENA-1 (NCT03616587) is a phase I, multipart, open-label study in women with refractory estrogen receptor-positive, HER2- advanced breast cancer. Patients received oral once-daily camizestrant 75 or 150 mg plus abemaciclib; camizestrant 75, 150, or 300 mg plus palbociclib; or camizestrant 75 mg plus ribociclib 400 or 600 mg. Safety/tolerability, pharmacokinetics, efficacy, and impact on estrogen receptor 1 mutation ctDNA were assessed.&#xd;
Results: By September 16, 2024 (data cutoff), 53 patients had received camizestrant plus abemaciclib, 78 camizestrant plus palbociclib, and 60 camizestrant plus ribociclib. Patients had a median of 2 (range, 0-7) prior regimens for advanced disease; 83% had received a prior CDK4/6i and 59% prior fulvestrant. The most common treatment-emergent adverse events for camizestrant 75 mg (phase III dose) plus each CDK4/6i were diarrhea [with abemaciclib (87.5%)] and neutropenia [with palbociclib (80%) and ribociclib (32.1% for 400 mg and 53.1% for 600 mg)]. The median camizestrant tmax was ∼4 hours postdose across combinations, with an estimated half-life of 9.5 to 17 hours. No clinically meaningful drug-drug interactions were evident. In this heavily pretreated population, CBR24 was 49.5% and the median progression-free survival was 7.4 months (95% confidence interval, 5.3-9.3), with antitumor activity across all combinations, including patients previously treated with CDK4/6i and/or fulvestrant, with or without estrogen receptor 1 mutation.&#xd;
Conclusions: Camizestrant is well tolerated, with antitumor activity in combination with CDK4/6i. These results support the evaluation of camizestrant 75 mg plus standard CDK4/6i doses in phase III trials.</dcterms:abstract>
   <dcterms:issued>2025-10-20T10:25:49Z</dcterms:issued>
   <dcterms:issued>2025-10-20T10:25:49Z</dcterms:issued>
   <dcterms:issued>2025-10-15</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:relation>Clinical Cancer Research;31(20)</dc:relation>
   <dc:relation>https://doi.org/10.1158/1078-0432.CCR-25-1198</dc:relation>
   <dc:rights>Attribution 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>American Association for Cancer Research</dc:publisher>
   <dc:source>Scientia</dc:source>
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