<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>28(20)</volume><submitter>Constantinidou A</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>The EndoPredict prognostic assay is validated to predict distant recurrence and response to chemotherapy primarily in post-menopausal women with estrogen receptor-positive (ER+), HER2- breast cancer. This study evaluated the performance of EndoPredict in pre-menopausal women.&lt;h4>Experimental design&lt;/h4>Tumor samples from 385 pre-menopausal women with ER+, HER2- primary breast cancer (pT1-3, pN0-1) who did not receive chemotherapy in addition to endocrine therapy were tested with EndoPredict to produce a 12-gene EP molecular score and an integrated EPclin score that includes pathologic tumor size and nodal status. Associations of molecular and EPclin scores with 10-year distant recurrence-free survival (DRFS) were evaluated by Cox proportional hazards models and Kaplan-Meier analysis.&lt;h4>Results&lt;/h4>After a median follow-up of 9.7 years, both the EP molecular score and the molecular-clinicopathologic EPclin score were associated with increased risk of distant recurrence [HR, 1.33; 95% confidence interval (CI), 1.18-1.50; P = 7.2 × 10-6; HR, 3.58; 95% CI, 2.26-5.66; P = 9.8 × 10-8, respectively]. Both scores remained significant after adjusting for clinical factors in multivariate analysis. Patients with low-risk EPclin scores (64.7%) had significantly improved DRFS compared with high-risk patients (HR, 4.61; 95% CI, 1.40-15.17; P = 4.2 × 10-3). At 10 years, patients with low-risk and high-risk EPclin scores had a DRFS of 97% (95% CI, 93%-99%) and 76% (95% CI, 67%-82%), respectively.&lt;h4>Conclusions&lt;/h4>The EPclin score is strongly associated with DRFS in pre-menopausal women who received adjuvant endocrine therapy alone. On the basis of these data, pre-menopausal women with EPclin low-risk breast cancer may be treated with endocrine therapy only and safely forgo adjuvant chemotherapy.</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pagination>4435-4443</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9561607</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clinical Validation of EndoPredict in Pre-Menopausal Women with ER-Positive, HER2-Negative Primary Breast Cancer.</pubmed_title><pmcid>PMC9561607</pmcid><pubmed_authors>Marcou Y</pubmed_authors><pubmed_authors>Doedt J</pubmed_authors><pubmed_authors>Slavin TP</pubmed_authors><pubmed_authors>Ellis IO</pubmed_authors><pubmed_authors>Bernhisel R</pubmed_authors><pubmed_authors>Constantinidou A</pubmed_authors><pubmed_authors>Simmons T</pubmed_authors><pubmed_authors>Probst B</pubmed_authors><pubmed_authors>Meek S</pubmed_authors><pubmed_authors>Wagner S</pubmed_authors><pubmed_authors>Kronenwett R</pubmed_authors><pubmed_authors>Toss MS</pubmed_authors><pubmed_authors>Georgiou G</pubmed_authors><pubmed_authors>Kuhl V</pubmed_authors><pubmed_authors>Gutin A</pubmed_authors><pubmed_authors>Hughes E</pubmed_authors><pubmed_authors>Lanchbury JS</pubmed_authors><pubmed_authors>Kakouri E</pubmed_authors><pubmed_authors>Rakha EA</pubmed_authors><pubmed_authors>Zouvani I</pubmed_authors><pubmed_authors>Savvidou G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical Validation of EndoPredict in Pre-Menopausal Women with ER-Positive, HER2-Negative Primary Breast Cancer.</name><description>&lt;h4>Purpose&lt;/h4>The EndoPredict prognostic assay is validated to predict distant recurrence and response to chemotherapy primarily in post-menopausal women with estrogen receptor-positive (ER+), HER2- breast cancer. This study evaluated the performance of EndoPredict in pre-menopausal women.&lt;h4>Experimental design&lt;/h4>Tumor samples from 385 pre-menopausal women with ER+, HER2- primary breast cancer (pT1-3, pN0-1) who did not receive chemotherapy in addition to endocrine therapy were tested with EndoPredict to produce a 12-gene EP molecular score and an integrated EPclin score that includes pathologic tumor size and nodal status. Associations of molecular and EPclin scores with 10-year distant recurrence-free survival (DRFS) were evaluated by Cox proportional hazards models and Kaplan-Meier analysis.&lt;h4>Results&lt;/h4>After a median follow-up of 9.7 years, both the EP molecular score and the molecular-clinicopathologic EPclin score were associated with increased risk of distant recurrence [HR, 1.33; 95% confidence interval (CI), 1.18-1.50; P = 7.2 × 10-6; HR, 3.58; 95% CI, 2.26-5.66; P = 9.8 × 10-8, respectively]. Both scores remained significant after adjusting for clinical factors in multivariate analysis. Patients with low-risk EPclin scores (64.7%) had significantly improved DRFS compared with high-risk patients (HR, 4.61; 95% CI, 1.40-15.17; P = 4.2 × 10-3). At 10 years, patients with low-risk and high-risk EPclin scores had a DRFS of 97% (95% CI, 93%-99%) and 76% (95% CI, 67%-82%), respectively.&lt;h4>Conclusions&lt;/h4>The EPclin score is strongly associated with DRFS in pre-menopausal women who received adjuvant endocrine therapy alone. On the basis of these data, pre-menopausal women with EPclin low-risk breast cancer may be treated with endocrine therapy only and safely forgo adjuvant chemotherapy.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-04-04T21:04:46.907Z</modification><creation>2025-04-04T21:04:46.907Z</creation></dates><accession>S-EPMC9561607</accession><cross_references><pubmed>36043530</pubmed><doi>10.1158/1078-0432.CCR-22-0619</doi></cross_references></HashMap>