<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>30(10)</volume><submitter>Goetz MP</submitter><funding>n/a</funding><pubmed_abstract>&lt;h4>Purpose&lt;/h4>To identify potential predictors of response and resistance mechanisms in patients with hormone receptor-positive (HR+), HER2-negative (HER2-) advanced breast cancer (ABC) treated with the cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitor abemaciclib ± endocrine therapy (ET), baseline and acquired genomic alterations in circulating tumor DNA (ctDNA) were analyzed and associated with clinical outcomes.&lt;h4>Experimental design&lt;/h4>MONARCH 3: postmenopausal women with HR+, HER2- ABC and no prior systemic therapy in the advanced setting were randomly assigned to abemaciclib or placebo plus nonsteroidal aromatase inhibitor (NSAI). nextMONARCH: women with HR+, HER2- metastatic breast cancer that progressed on/after prior ET and chemotherapy were randomly assigned to abemaciclib a</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pagination>2233-2244</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11094424</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Landscape of Baseline and Acquired Genomic Alterations in Circulating Tumor DNA with Abemaciclib Alone or with Endocrine Therapy in Advanced Breast Cancer.</pubmed_title><pmcid>PMC11094424</pmcid><pubmed_authors>Graham H</pubmed_authors><pubmed_authors>Campone M</pubmed_authors><pubmed_authors>Jerusalem G</pubmed_authors><pubmed_authors>Toi M</pubmed_authors><pubmed_authors>Hamilton EP</pubmed_authors><pubmed_authors>Hurvitz SA</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Llombart-Cussac A</pubmed_authors><pubmed_authors>Jansen VM</pubmed_authors><pubmed_authors>Litchfield LM</pubmed_authors><pubmed_authors>Goetz MP</pubmed_authors><pubmed_authors>Cortes J</pubmed_authors><pubmed_authors>Martin M</pubmed_authors><pubmed_authors>Johnston S</pubmed_authors><pubmed_authors>Kaufman PA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Landscape of Baseline and Acquired Genomic Alterations in Circulating Tumor DNA with Abemaciclib Alone or with Endocrine Therapy in Advanced Breast Cancer.</name><description>&lt;h4>Purpose&lt;/h4>To identify potential predictors of response and resistance mechanisms in patients with hormone receptor-positive (HR+), HER2-negative (HER2-) advanced breast cancer (ABC) treated with the cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitor abemaciclib ± endocrine therapy (ET), baseline and acquired genomic alterations in circulating tumor DNA (ctDNA) were analyzed and associated with clinical outcomes.&lt;h4>Experimental design&lt;/h4>MONARCH 3: postmenopausal women with HR+, HER2- ABC and no prior systemic therapy in the advanced setting were randomly assigned to abemaciclib or placebo plus nonsteroidal aromatase inhibitor (NSAI). nextMONARCH: women with HR+, HER2- metastatic breast cancer that progressed on/after prior ET and chemotherapy were randomly assigned to abemaciclib a</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-06-02T01:42:05.76Z</modification><creation>2026-04-13T03:12:01.704Z</creation></dates><accession>S-EPMC11094424</accession><cross_references><pubmed>37889120</pubmed><doi>10.1158/1078-0432.CCR-22-3573</doi></cross_references></HashMap>