<?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>2026-04-13T01:33:15Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/8091" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/8091</identifier><datestamp>2025-10-25T05:36:50Z</datestamp><setSpec>com_2072_378072</setSpec><setSpec>com_2072_378040</setSpec><setSpec>col_2072_378100</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" 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://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Sacituzumab govitecan as second-line treatment for metastatic triple-negative breast cancer—phase 3 ASCENT study subanalysis</dc:title>
   <dc:creator>Carey, Lisa</dc:creator>
   <dc:creator>Loirat, Delphine</dc:creator>
   <dc:creator>Dieras, Veronique</dc:creator>
   <dc:creator>Cortés Castan, Javier</dc:creator>
   <dc:creator>Bardia, Aditya</dc:creator>
   <dc:creator>Punie, Kevin</dc:creator>
   <dc:creator>Dalenc, Florence</dc:creator>
   <dc:subject>Mama - Càncer - Tractament</dc:subject>
   <dc:subject>Anticossos monoclonals - Ús terapèutic</dc:subject>
   <dc:subject>DISEASES::Neoplasms::Neoplasms by Site::Breast Neoplasms::Triple Negative Breast Neoplasms</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::Other subheadings::/drug therapy</dc:subject>
   <dc:subject>CHEMICALS AND DRUGS::Amino Acids, Peptides, and Proteins::Proteins::Blood Proteins::Serum Globulins::Immunoglobulins::Antibodies::Immunoconjugates</dc:subject>
   <dc:subject>ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de la mama::neoplasias de mama triple negativos</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia</dc:subject>
   <dc:subject>COMPUESTOS QUÍMICOS Y DROGAS::aminoácidos, péptidos y proteínas::proteínas::proteínas sanguíneas::globulinas séricas::inmunoglobulinas::anticuerpos::inmunoconjugados</dc:subject>
   <dcterms:abstract>Breast cancer; Second-line treatment</dcterms:abstract>
   <dcterms:abstract>Cáncer de mama; Tratamiento de segunda línea</dcterms:abstract>
   <dcterms:abstract>Càncer de mama; Tractament de segona línia</dcterms:abstract>
   <dcterms:abstract>Patients with triple-negative breast cancer (TNBC) who relapse early after (neo)adjuvant chemotherapy have more aggressive disease. In the ASCENT trial, sacituzumab govitecan (SG), an antibody-drug conjugate composed of an anti-Trop–2 antibody coupled to SN-38 via a hydrolyzable linker, improved outcomes over single-agent chemotherapy of physician’s choice (TPC) in metastatic TNBC (mTNBC). Of 468 patients without known baseline brain metastases, 33/235 vs 32/233 patients (both 14%) in the SG vs TPC arms, respectively, received one line of therapy in the metastatic setting and experienced disease recurrence ≤12 months after (neo)adjuvant chemotherapy. SG prolonged progression-free survival (median 5.7 vs 1.5 months [HR, 0.41; 95% CI, 0.22–0.76]) and overall survival (median 10.9 vs 4.9 months [HR, 0.51; 95% CI, 0.28–0.91]) vs TPC, with a manageable safety profile in this subgroup consistent with the overall population. In this second-line setting, as with later-line therapy, SG improved survival over conventional chemotherapy for patients with mTNBC.</dcterms:abstract>
   <dcterms:abstract>This study was sponsored by Gilead Sciences, Inc.</dcterms:abstract>
   <dcterms:dateAccepted>2025-10-25T05:36:50Z</dcterms:dateAccepted>
   <dcterms:available>2025-10-25T05:36:50Z</dcterms:available>
   <dcterms:created>2025-10-25T05:36:50Z</dcterms:created>
   <dcterms:issued>2022-09-09T07:45:33Z</dcterms:issued>
   <dcterms:issued>2022-09-09T07:45:33Z</dcterms:issued>
   <dcterms:issued>2022-06-09</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>http://hdl.handle.net/11351/8091</dc:identifier>
   <dc:relation>NPJ Breast Cancer;8</dc:relation>
   <dc:relation>https://doi.org/10.1038/s41523-022-00439-5</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>Nature Research</dc:publisher>
   <dc:source>Scientia</dc:source>
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