<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(1)</volume><submitter>Carey LA</submitter><funding>Gilead Sciences, Inc.</funding><pubmed_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 mont</pubmed_abstract><journal>NPJ breast cancer</journal><pagination>72</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9184615</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Sacituzumab govitecan as second-line treatment for metastatic triple-negative breast cancer-phase 3 ASCENT study subanalysis.</pubmed_title><pmcid>PMC9184615</pmcid><pubmed_authors>Rugo HS</pubmed_authors><pubmed_authors>Zhu Y</pubmed_authors><pubmed_authors>Diamond JR</pubmed_authors><pubmed_authors>Fontaine C</pubmed_authors><pubmed_authors>Punie K</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Kalinsky K</pubmed_authors><pubmed_authors>Dalenc F</pubmed_authors><pubmed_authors>Hurvitz SA</pubmed_authors><pubmed_authors>Loirat D</pubmed_authors><pubmed_authors>Bardia A</pubmed_authors><pubmed_authors>Dieras V</pubmed_authors><pubmed_authors>Phan S</pubmed_authors><pubmed_authors>Piccart M</pubmed_authors><pubmed_authors>Carey LA</pubmed_authors><pubmed_authors>Delaney R</pubmed_authors><pubmed_authors>O'Shaughnessy J</pubmed_authors><pubmed_authors>Loibl S</pubmed_authors><pubmed_authors>Cortes J</pubmed_authors><pubmed_authors>Gianni L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sacituzumab govitecan as second-line treatment for metastatic triple-negative breast cancer-phase 3 ASCENT study subanalysis.</name><description>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 mont</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2025-04-04T13:17:13.658Z</modification><creation>2025-02-19T04:56:36.726Z</creation></dates><accession>S-EPMC9184615</accession><cross_references><pubmed>35680967</pubmed><doi>10.1038/s41523-022-00439-5</doi></cross_references></HashMap>