<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>102</volume><submitter>Conte B</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Early-stage triple-negative breast cancer (TNBC) displays clinical and biological diversity. From a biological standpoint, immune infiltration plays a crucial role in TNBC prognosis. Currently, there is a lack of genomic tools aiding in treatment decisions for TNBC. This study aims to assess the effectiveness of a B-cell/immunoglobulin signature (IGG) alone, or in combination with tumor burden, in predicting prognosis and treatment response in patients with TNBC.&lt;h4>Methods&lt;/h4>Genomic and clinical data were retrieved from 7 cohorts: SCAN-B (N = 874), BrighTNess (n = 482), CALGB-40603 (n = 389), METABRIC (n = 267), TCGA (n = 118), GSE58812 (n = 107), GSE21653 (n = 67). IGG and a risk score integrating IGG with tumor/nodal staging (IGG-Clin) were assessed for event-free s</pubmed_abstract><journal>EBioMedicine</journal><pagination>105043</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10924177</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A 14-gene B-cell immune signature in early-stage triple-negative breast cancer (TNBC): a pooled analysis of seven studies.</pubmed_title><pmcid>PMC10924177</pmcid><pubmed_authors>Prat A</pubmed_authors><pubmed_authors>Martinez-Saez O</pubmed_authors><pubmed_authors>Parker JS</pubmed_authors><pubmed_authors>Falato C</pubmed_authors><pubmed_authors>Perou CM</pubmed_authors><pubmed_authors>Schettini F</pubmed_authors><pubmed_authors>Segui E</pubmed_authors><pubmed_authors>Garcia-Fructuoso I</pubmed_authors><pubmed_authors>Villacampa G</pubmed_authors><pubmed_authors>Staaf J</pubmed_authors><pubmed_authors>Vivancos A</pubmed_authors><pubmed_authors>Conte B</pubmed_authors><pubmed_authors>Lorman-Carbo N</pubmed_authors><pubmed_authors>Angelats L</pubmed_authors><pubmed_authors>Adamo B</pubmed_authors><pubmed_authors>Fratini B</pubmed_authors><pubmed_authors>Vidal Losada MJ</pubmed_authors><pubmed_authors>Hernandez AR</pubmed_authors><pubmed_authors>Sanfeliu E</pubmed_authors><pubmed_authors>Braso-Maristany F</pubmed_authors><pubmed_authors>Chic N</pubmed_authors><pubmed_authors>Gomez-Bravo R</pubmed_authors><pubmed_authors>Villagrasa P</pubmed_authors><pubmed_authors>Marin-Aguilera M</pubmed_authors><pubmed_authors>Pascual T</pubmed_authors><pubmed_authors>Pare L</pubmed_authors></additional><is_claimable>false</is_claimable><name>A 14-gene B-cell immune signature in early-stage triple-negative breast cancer (TNBC): a pooled analysis of seven studies.</name><description>&lt;h4>Background&lt;/h4>Early-stage triple-negative breast cancer (TNBC) displays clinical and biological diversity. From a biological standpoint, immune infiltration plays a crucial role in TNBC prognosis. Currently, there is a lack of genomic tools aiding in treatment decisions for TNBC. This study aims to assess the effectiveness of a B-cell/immunoglobulin signature (IGG) alone, or in combination with tumor burden, in predicting prognosis and treatment response in patients with TNBC.&lt;h4>Methods&lt;/h4>Genomic and clinical data were retrieved from 7 cohorts: SCAN-B (N = 874), BrighTNess (n = 482), CALGB-40603 (n = 389), METABRIC (n = 267), TCGA (n = 118), GSE58812 (n = 107), GSE21653 (n = 67). IGG and a risk score integrating IGG with tumor/nodal staging (IGG-Clin) were assessed for event-free s</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-05-29T12:28:04.861Z</modification><creation>2024-11-09T19:15:58.109Z</creation></dates><accession>S-EPMC10924177</accession><cross_references><pubmed>38447275</pubmed><doi>10.1016/j.ebiom.2024.105043</doi></cross_references></HashMap>