<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wapnir IL</submitter><funding>NCI NIH HHS</funding><pagination>1073-1079</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5891132</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>36(11)</volume><pubmed_abstract>Purpose Isolated locoregional recurrence (ILRR) predicts a high risk of developing breast cancer distant metastases and death. The Chemotherapy as Adjuvant for LOcally Recurrent breast cancer (CALOR) trial investigated the effectiveness of chemotherapy (CT) after local therapy for ILRR. A report at 5 years of median follow-up showed significant benefit of CT for estrogen receptor (ER)-negative ILRR, but additional follow-up was required in ER-positive ILRR. Patients and Methods CALOR was an open-label, randomized trial for patients with completely excised ILRR after unilateral breast cancer. Eligible patients were randomly assigned to receive CT or no CT and stratified by prior CT, hormone receptor status, and location of ILRR. Patients with hormone receptor-positive ILRR received adjuvant</pubmed_abstract><journal>Journal of clinical oncology : official journal of the American Society of Clinical Oncology</journal><pubmed_title>Efficacy of Chemotherapy for ER-Negative and ER-Positive Isolated Locoregional Recurrence of Breast Cancer: Final Analysis of the CALOR Trial.</pubmed_title><pmcid>PMC5891132</pmcid><funding_grant_id>UG1 CA189867</funding_grant_id><funding_grant_id>U10 CA180868</funding_grant_id><funding_grant_id>U10 CA180822</funding_grant_id><pubmed_authors>Gelber RD</pubmed_authors><pubmed_authors>NRG Oncology, GEICAM Spanish Breast Cancer Group, BOOG Dutch Breast Cancer Trialists' Group</pubmed_authors><pubmed_authors>Breast International Group</pubmed_authors><pubmed_authors>Price KN</pubmed_authors><pubmed_authors>Wapnir IL</pubmed_authors><pubmed_authors>Anderson SJ</pubmed_authors><pubmed_authors>Rimawi MF</pubmed_authors><pubmed_authors>Lang I</pubmed_authors><pubmed_authors>Paterson AHG</pubmed_authors><pubmed_authors>Baena-Canada JM</pubmed_authors><pubmed_authors>Thurlimann B</pubmed_authors><pubmed_authors>Aebi S</pubmed_authors><pubmed_authors>Mamounas EP</pubmed_authors><pubmed_authors>Robidoux A</pubmed_authors><pubmed_authors>Rastogi P</pubmed_authors><pubmed_authors>Martin M</pubmed_authors><pubmed_authors>Coates AS</pubmed_authors><pubmed_authors>Geyer CE</pubmed_authors><pubmed_authors>Gelber S</pubmed_authors><pubmed_authors>Regan MM</pubmed_authors><pubmed_authors>Nortier JWR</pubmed_authors><pubmed_authors>Wolmark N</pubmed_authors><pubmed_authors>International Breast Cancer Study Group</pubmed_authors></additional><is_claimable>false</is_claimable><name>Efficacy of Chemotherapy for ER-Negative and ER-Positive Isolated Locoregional Recurrence of Breast Cancer: Final Analysis of the CALOR Trial.</name><description>Purpose Isolated locoregional recurrence (ILRR) predicts a high risk of developing breast cancer distant metastases and death. The Chemotherapy as Adjuvant for LOcally Recurrent breast cancer (CALOR) trial investigated the effectiveness of chemotherapy (CT) after local therapy for ILRR. A report at 5 years of median follow-up showed significant benefit of CT for estrogen receptor (ER)-negative ILRR, but additional follow-up was required in ER-positive ILRR. Patients and Methods CALOR was an open-label, randomized trial for patients with completely excised ILRR after unilateral breast cancer. Eligible patients were randomly assigned to receive CT or no CT and stratified by prior CT, hormone receptor status, and location of ILRR. Patients with hormone receptor-positive ILRR received adjuvant</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Apr</publication><modification>2025-06-01T03:45:49.233Z</modification><creation>2019-10-28T11:16:12Z</creation></dates><accession>S-EPMC5891132</accession><cross_references><pubmed>29443653</pubmed><doi>10.1200/jco.2017.76.5719</doi><doi>10.1200/JCO.2017.76.5719</doi></cross_references></HashMap>