<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>77</volume><submitter>Bar Y</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Early invasive ductal carcinoma (IDC) breast cancer often presents with a coexisting ductal carcinoma in situ (DCIS) component, while about 5 % of cases present with an extensive (>25 %) intraductal component (EIC). The impact of EIC on the genomic risk of recurrence is unclear.&lt;h4>Methods&lt;/h4>Patients with early hormone receptor-positive HER2neu-negative (HR + HER2-) IDC breast cancer and a known OncotypeDX Breast Recurrence Score® (RS) who underwent breast surgery at our institute were included. Using a rule-based text-analysis algorithm, we analyzed pathological reports and categorized patients into three groups: EIC, non-extensive DCIS (DCIS-L), and pure-IDC (NO-DCIS). Genomic risk was determined using OncotypeDX RS.&lt;h4>Results&lt;/h4>A total of 33 (4.6 %) EIC cases, 37</pubmed_abstract><journal>Breast (Edinburgh, Scotland)</journal><pagination>103777</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11325798</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The impact of extensive intraductal component (EIC) on the genomic risk of recurrence in early hormone receptor positive breast cancer.</pubmed_title><pmcid>PMC11325798</pmcid><pubmed_authors>Bar K</pubmed_authors><pubmed_authors>Lerner S</pubmed_authors><pubmed_authors>Shahoha M</pubmed_authors><pubmed_authors>Bar Y</pubmed_authors><pubmed_authors>Shachar SS</pubmed_authors><pubmed_authors>Dershowitz N</pubmed_authors><pubmed_authors>Feldman D</pubmed_authors><pubmed_authors>Dror JB</pubmed_authors><pubmed_authors>Sonnenblick A</pubmed_authors><pubmed_authors>Weiss-Meilik A</pubmed_authors><pubmed_authors>Wolf I</pubmed_authors></additional><is_claimable>false</is_claimable><name>The impact of extensive intraductal component (EIC) on the genomic risk of recurrence in early hormone receptor positive breast cancer.</name><description>&lt;h4>Background&lt;/h4>Early invasive ductal carcinoma (IDC) breast cancer often presents with a coexisting ductal carcinoma in situ (DCIS) component, while about 5 % of cases present with an extensive (>25 %) intraductal component (EIC). The impact of EIC on the genomic risk of recurrence is unclear.&lt;h4>Methods&lt;/h4>Patients with early hormone receptor-positive HER2neu-negative (HR + HER2-) IDC breast cancer and a known OncotypeDX Breast Recurrence Score® (RS) who underwent breast surgery at our institute were included. Using a rule-based text-analysis algorithm, we analyzed pathological reports and categorized patients into three groups: EIC, non-extensive DCIS (DCIS-L), and pure-IDC (NO-DCIS). Genomic risk was determined using OncotypeDX RS.&lt;h4>Results&lt;/h4>A total of 33 (4.6 %) EIC cases, 37</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2025-04-21T22:07:14.115Z</modification><creation>2025-04-05T18:35:00.075Z</creation></dates><accession>S-EPMC11325798</accession><cross_references><pubmed>39038425</pubmed><doi>10.1016/j.breast.2024.103777</doi></cross_references></HashMap>