<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wu W</submitter><funding>Sun Yat-Sen University Clinical Research 5010 Programme</funding><pagination>497</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5655944</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The response to neoadjuvant chemotherapy (NAC) varies by estrogen receptor (ER) and human epidermal growth factor receptor 2 (HER2) statuses, with responses being lower in ER-positive, HER2-negative tumors as compared with ER-negative, HER2-positive or triple-negative tumors. Neoadjuvant endocrine therapy (NET) is an attractive alternative to NAC for ER-positive, HER2-negative cancer. However, a prior trial comparing NET with standard NAC in ER-positive tumor showed that the difference of response was not significant. Studies demonstrated that the mTOR inhibitor everolimus could sensitize breast tumors to endocrine therapy. A pilot open-label, randomized trial has been designed to evaluate the feasibility, efficacy and tolerability of neoadjuvant everolimus plus letrozol</pubmed_abstract><journal>Trials</journal><pubmed_title>Neoadjuvant everolimus plus letrozole versus fluorouracil, epirubicin and cyclophosphamide for ER-positive, HER2-negative breast cancer: study protocol for a randomized pilot trial.</pubmed_title><pmcid>PMC5655944</pmcid><funding_grant_id>2016015</funding_grant_id><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Cao M</pubmed_authors><pubmed_authors>You N</pubmed_authors><pubmed_authors>Wu W</pubmed_authors><pubmed_authors>Deng H</pubmed_authors><pubmed_authors>Rao N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Neoadjuvant everolimus plus letrozole versus fluorouracil, epirubicin and cyclophosphamide for ER-positive, HER2-negative breast cancer: study protocol for a randomized pilot trial.</name><description>&lt;h4>Background&lt;/h4>The response to neoadjuvant chemotherapy (NAC) varies by estrogen receptor (ER) and human epidermal growth factor receptor 2 (HER2) statuses, with responses being lower in ER-positive, HER2-negative tumors as compared with ER-negative, HER2-positive or triple-negative tumors. Neoadjuvant endocrine therapy (NET) is an attractive alternative to NAC for ER-positive, HER2-negative cancer. However, a prior trial comparing NET with standard NAC in ER-positive tumor showed that the difference of response was not significant. Studies demonstrated that the mTOR inhibitor everolimus could sensitize breast tumors to endocrine therapy. A pilot open-label, randomized trial has been designed to evaluate the feasibility, efficacy and tolerability of neoadjuvant everolimus plus letrozol</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Oct</publication><modification>2026-06-08T05:43:43.157Z</modification><creation>2019-03-27T02:59:52Z</creation></dates><accession>S-EPMC5655944</accession><cross_references><pubmed>29070044</pubmed><doi>10.1186/s13063-017-2228-5</doi></cross_references></HashMap>