<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15</volume><submitter>Rahal S</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Anthracycline-based adjuvant chemotherapy improves survival in patients with high-risk node-negative breast cancer (BC). In this setting, prognostic factors predicting for treatment failure might help selecting among the different available cytotoxic combinations.&lt;h4>Methods&lt;/h4>Between 1998 and 2008, 757 consecutive patients with node-negative BC treated in our institution with adjuvant FEC (5FU, epirubicin, cyclophosphamide) chemotherapy were identified. Data collection included demographic, clinico-pathological characteristics and treatment information. Molecular subtypes were derived from estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2) status and Scarff-Bloom-Richardson (SBR) grade. Disease-free survival (DFS), dist</pubmed_abstract><journal>BMC cancer</journal><pagination>697</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4607139</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Immunohistochemical subtypes predict the clinical outcome in high-risk node-negative breast cancer patients treated with adjuvant FEC regimen: results of a single-center retrospective study.</pubmed_title><pmcid>PMC4607139</pmcid><pubmed_authors>Resbeut M</pubmed_authors><pubmed_authors>Viens P</pubmed_authors><pubmed_authors>Lambaudie E</pubmed_authors><pubmed_authors>Houvenaeghel G</pubmed_authors><pubmed_authors>Boher JM</pubmed_authors><pubmed_authors>Thomassin-Piana J</pubmed_authors><pubmed_authors>Goncalves A</pubmed_authors><pubmed_authors>Charafe-Jauffret E</pubmed_authors><pubmed_authors>Bertucci F</pubmed_authors><pubmed_authors>Tarpin C</pubmed_authors><pubmed_authors>Extra JM</pubmed_authors><pubmed_authors>Tallet A</pubmed_authors><pubmed_authors>Sabatier R</pubmed_authors><pubmed_authors>Laborde L</pubmed_authors><pubmed_authors>Rahal S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immunohistochemical subtypes predict the clinical outcome in high-risk node-negative breast cancer patients treated with adjuvant FEC regimen: results of a single-center retrospective study.</name><description>&lt;h4>Background&lt;/h4>Anthracycline-based adjuvant chemotherapy improves survival in patients with high-risk node-negative breast cancer (BC). In this setting, prognostic factors predicting for treatment failure might help selecting among the different available cytotoxic combinations.&lt;h4>Methods&lt;/h4>Between 1998 and 2008, 757 consecutive patients with node-negative BC treated in our institution with adjuvant FEC (5FU, epirubicin, cyclophosphamide) chemotherapy were identified. Data collection included demographic, clinico-pathological characteristics and treatment information. Molecular subtypes were derived from estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2) status and Scarff-Bloom-Richardson (SBR) grade. Disease-free survival (DFS), dist</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Oct</publication><modification>2026-07-15T16:27:59.289Z</modification><creation>2026-07-07T03:07:55.804Z</creation></dates><accession>S-EPMC4607139</accession><cross_references><pubmed>26466893</pubmed><doi>10.1186/s12885-015-1746-3</doi></cross_references></HashMap>