<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(1)</volume><submitter>Goetz MP</submitter><funding>Eli Lilly and company</funding><funding>Eli lilly and company</funding><funding>Eli Lilly and Company</funding><pubmed_abstract>In monarchE, adjuvant abemaciclib significantly improved invasive disease-free survival (IDFS) and distant relapse-free survival (DRFS), with sustained benefit beyond the 2-year treatment period. Abemaciclib dose reductions were allowed to proactively manage adverse events. Exploratory analyses to investigate the impact of dose reductions on efficacy were conducted. Across the three patient subgroups as defined by relative dose intensity (≤66%, 66-93%, ≥93%), the estimated 4-year IDFS rates were generally consistent (87.1%, 86.4%, and 83.7%, respectively). In the time-dependent Cox proportional hazard model, the effect of abemaciclib was consistent at the full dose compared to being reduced to a lower dose (IDFS hazard ratio: 0.905; 95% confidence interval: 0.727, 1.125; DRFS hazard ratio:</pubmed_abstract><journal>NPJ breast cancer</journal><pagination>34</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11053007</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Impact of dose reductions on adjuvant abemaciclib efficacy for patients with high-risk early breast cancer: analyses from the monarchE study.</pubmed_title><pmcid>PMC11053007</pmcid><pubmed_authors>Andre V</pubmed_authors><pubmed_authors>Harbeck N</pubmed_authors><pubmed_authors>Rugo HS</pubmed_authors><pubmed_authors>Johnston SRD</pubmed_authors><pubmed_authors>Testa L</pubmed_authors><pubmed_authors>Tolaney SM</pubmed_authors><pubmed_authors>Guarneri V</pubmed_authors><pubmed_authors>Wei R</pubmed_authors><pubmed_authors>O'Shaughnessy J</pubmed_authors><pubmed_authors>Cicin I</pubmed_authors><pubmed_authors>Rastogi P</pubmed_authors><pubmed_authors>Goetz MP</pubmed_authors><pubmed_authors>Huober J</pubmed_authors><pubmed_authors>Martin M</pubmed_authors><pubmed_authors>Shahir A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of dose reductions on adjuvant abemaciclib efficacy for patients with high-risk early breast cancer: analyses from the monarchE study.</name><description>In monarchE, adjuvant abemaciclib significantly improved invasive disease-free survival (IDFS) and distant relapse-free survival (DRFS), with sustained benefit beyond the 2-year treatment period. Abemaciclib dose reductions were allowed to proactively manage adverse events. Exploratory analyses to investigate the impact of dose reductions on efficacy were conducted. Across the three patient subgroups as defined by relative dose intensity (≤66%, 66-93%, ≥93%), the estimated 4-year IDFS rates were generally consistent (87.1%, 86.4%, and 83.7%, respectively). In the time-dependent Cox proportional hazard model, the effect of abemaciclib was consistent at the full dose compared to being reduced to a lower dose (IDFS hazard ratio: 0.905; 95% confidence interval: 0.727, 1.125; DRFS hazard ratio:</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-06-02T02:13:42.13Z</modification><creation>2026-04-13T03:12:50.712Z</creation></dates><accession>S-EPMC11053007</accession><cross_references><pubmed>38671001</pubmed><doi>10.1038/s41523-024-00639-1</doi></cross_references></HashMap>