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               <dc:title>Safety overview and management of inavolisib alone and in combination therapies in PIK3CA-mutated, HR-positive, HER2-negative advanced breast cancer (GO39374)</dc:title>
               <dc:creator>ITALIANO, ANTOINE</dc:creator>
               <dc:creator>Gambardella, Valentina</dc:creator>
               <dc:creator>Accordino, Melissa</dc:creator>
               <dc:creator>Bedard, Philippe</dc:creator>
               <dc:creator>Cervantes, Andrés</dc:creator>
               <dc:creator>Hamilton, Erika</dc:creator>
               <dc:creator>Oliveira, Mafalda</dc:creator>
               <dc:creator>Saura Manich, Cristina</dc:creator>
               <dc:subject>Anomalies cromosòmiques</dc:subject>
               <dc:subject>Enzims - Inhibidors - Ús terapèutic</dc:subject>
               <dc:subject>Enzims - Inhibidors - Ús terapèutic</dc:subject>
               <dc:subject>Quimioteràpia combinada</dc:subject>
               <dc:subject>Mama - Càncer - Tractament</dc:subject>
               <dc:subject>PHENOMENA AND PROCESSES::Genetic Phenomena::Genetic Variation::Mutation</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>DISEASES::Neoplasms::Neoplasms by Site::Breast Neoplasms</dc:subject>
               <dc:subject>Other subheadings::Other subheadings::Other subheadings::/drug therapy</dc:subject>
               <dc:subject>CHEMICALS AND DRUGS::Enzymes and Coenzymes::Enzymes::Transferases::Phosphotransferases::Phosphotransferases (Alcohol Group Acceptor)::Phosphatidylinositol 3-Kinases</dc:subject>
               <dc:subject>Other subheadings::Other subheadings::Other subheadings::/antagonists &amp; inhibitors</dc:subject>
               <dc:subject>FENÓMENOS Y PROCESOS::fenómenos genéticos::variación genética::mutación</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>ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de la mama</dc:subject>
               <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia</dc:subject>
               <dc:subject>COMPUESTOS QUÍMICOS Y DROGAS::enzimas y coenzimas::enzimas::transferasas::fosfotransferasas::fosfotransferasas (grupo alcohol aceptor)::fosfatidil inositol 3 cinasas</dc:subject>
               <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/antagonistas &amp; inhibidores</dc:subject>
               <dc:description>PI3K inhibitor; Breast cancer; Hormone receptor-positive</dc:description>
               <dc:description>Inhibidor de PI3K; Càncer de mama; Receptor hormonal positiu</dc:description>
               <dc:description>Inhibidor de PI3K; Cáncer de mama; Receptor hormonal positivo</dc:description>
               <dc:description>Background: Inavolisib is a potent and selective PI3Kα inhibitor that promotes degradation of mutated p110α. We report safety from a phase I/Ib dose-escalation/-expansion study (GO39374; NCT03006172) of inavolisib alone or in combination therapies in PIK3CA-mutated, hormone receptor (HR)-positive, HER2-negative advanced breast cancer.&#xd;
Patients and methods: Patients received inavolisib [oral once daily (od)] alone, with letrozole (2.5 mg od) or fulvestrant (500 mg intramuscularly 4 weekly) ± palbociclib (125 mg od for 21/28 days); metformin was included in one arm.&#xd;
Primary endpoint: safety and tolerability.&#xd;
Results: At data cutoff (1 January 2024), 190 patients had been treated, of which 179 (94.2%) had discontinued study treatment, mainly due to progressive disease [146 (76.8%)]. Treatment-related any-grade and grade 3-5 adverse events (AEs) occurred in 181 (95.3%) and 107 (56.3%) patients, respectively. Inavolisib-related AEs led to inavolisib withdrawal in 5 (2.6%) and dose reductions/interruptions in 103 (54.2%) patients. Hyperglycemia, diarrhea, stomatitis (grouped terms), and rash (grouped terms) occurred in 129 (67.9%), 124 (65.3%), 93 (48.9%), and 47 (24.7%) patients, respectively. Hyperglycemia, diarrhea, and stomatitis mainly occurred early in treatment, and were manageable with supportive measures (including oral antihyperglycemic agents, common antidiarrheal medications, and dexamethasone mouthwash, respectively) and/or inavolisib dose modifications (dose interruptions with or without dose reductions). Hyperglycemia remained frequent in patients with risk factors, despite early metformin treatment. Rash was mostly grade 1 and required no treatment. Patients treated for ≥1 year [n = 65 (34.2%)] demonstrated encouraging long-term tolerability.&#xd;
Conclusions: Inavolisib alone or in combination with HR-positive breast cancer therapies demonstrated a manageable safety and tolerability profile, which supports its ongoing development.</dc:description>
               <dc:description>This work was supported by Genentech, Inc., South San Francisco, CA; and the Memorial Sloan Kettering Cancer Center [support grant number P30 CA008748].</dc:description>
               <dc:date>2025-09-30T02:07:00Z</dc:date>
               <dc:date>2025-09-30T02:07:00Z</dc:date>
               <dc:date>2025-08-07T08:31:05Z</dc:date>
               <dc:date>2025-08-07T08:31:05Z</dc:date>
               <dc:date>2025-07</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:identifier>http://hdl.handle.net/11351/13505</dc:identifier>
               <dc:relation>ESMO Open;10(7)</dc:relation>
               <dc:relation>https://doi.org/10.1016/j.esmoop.2025.105303</dc:relation>
               <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Elsevier</dc:publisher>
               <dc:source>Scientia</dc:source>
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