<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(11)</volume><submitter>O'Regan RM</submitter><pubmed_abstract>&lt;h4>Importance&lt;/h4>The Breast Cancer Index (BCI) previously identified premenopausal patients with tumors in which the ratio of expression of HOXB13 relative to IL17BR (hereafter, BCI [H/I]-low tumors) as likely to derive greatest benefit from ovarian function suppression (OFS)-containing adjuvant therapy in the Suppression of Ovarian Function Trial (SOFT) trial.&lt;h4>Objectives&lt;/h4>To assess BCI as a predictive biomarker of benefit from exemestane plus OFS vs tamoxifen plus OFS and to validate BCI as a prognostic biomarker for premenopausal patients.&lt;h4>Design, setting, and participants&lt;/h4>This prognostic study used a prospective-retrospective translational design within the Tamoxifen and Exemestane (TEXT) and SOFT trials (enrolled November 2003 to April 2011). Blinded BCI testing in all a</pubmed_abstract><journal>JAMA network open</journal><pagination>e2540931</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12584034</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Assessment of Adjuvant Endocrine Therapy With Ovarian Function Suppression by Breast Cancer Index.</pubmed_title><pmcid>PMC12584034</pmcid><pubmed_authors>Viale G</pubmed_authors><pubmed_authors>Salim M</pubmed_authors><pubmed_authors>Siuliukina N</pubmed_authors><pubmed_authors>Gomez HL</pubmed_authors><pubmed_authors>Ren Y</pubmed_authors><pubmed_authors>Francis PA</pubmed_authors><pubmed_authors>Walley BA</pubmed_authors><pubmed_authors>O'Regan RM</pubmed_authors><pubmed_authors>Treuner K</pubmed_authors><pubmed_authors>Lang I</pubmed_authors><pubmed_authors>Fleming GF</pubmed_authors><pubmed_authors>Schnabel CA</pubmed_authors><pubmed_authors>Chini C</pubmed_authors><pubmed_authors>Loibl S</pubmed_authors><pubmed_authors>Munzone E</pubmed_authors><pubmed_authors>Geyer CE</pubmed_authors><pubmed_authors>Dell'Orto P</pubmed_authors><pubmed_authors>Bonnefoi HR</pubmed_authors><pubmed_authors>Puglisi F</pubmed_authors><pubmed_authors>Nicoletti SVL</pubmed_authors><pubmed_authors>Kammler R</pubmed_authors><pubmed_authors>Tondini C</pubmed_authors><pubmed_authors>Colleoni M</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Zaman K</pubmed_authors><pubmed_authors>Ciruelos EM</pubmed_authors><pubmed_authors>Goetz MP</pubmed_authors><pubmed_authors>Loi S</pubmed_authors><pubmed_authors>Martino S</pubmed_authors><pubmed_authors>Stearns V</pubmed_authors><pubmed_authors>Pagani O</pubmed_authors><pubmed_authors>Regan MM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Assessment of Adjuvant Endocrine Therapy With Ovarian Function Suppression by Breast Cancer Index.</name><description>&lt;h4>Importance&lt;/h4>The Breast Cancer Index (BCI) previously identified premenopausal patients with tumors in which the ratio of expression of HOXB13 relative to IL17BR (hereafter, BCI [H/I]-low tumors) as likely to derive greatest benefit from ovarian function suppression (OFS)-containing adjuvant therapy in the Suppression of Ovarian Function Trial (SOFT) trial.&lt;h4>Objectives&lt;/h4>To assess BCI as a predictive biomarker of benefit from exemestane plus OFS vs tamoxifen plus OFS and to validate BCI as a prognostic biomarker for premenopausal patients.&lt;h4>Design, setting, and participants&lt;/h4>This prognostic study used a prospective-retrospective translational design within the Tamoxifen and Exemestane (TEXT) and SOFT trials (enrolled November 2003 to April 2011). Blinded BCI testing in all a</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-05T11:49:27.182Z</modification><creation>2026-05-16T03:13:31.228Z</creation></dates><accession>S-EPMC12584034</accession><cross_references><pubmed>41182766</pubmed><doi>10.1001/jamanetworkopen.2025.40931</doi></cross_references></HashMap>