<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Diaz-Anton B</submitter><funding>European Social Fund</funding><funding>Instituto de Salud Carlos III</funding><funding>Comunidad de Madrid</funding><pagination>1127-1137</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8934964</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(2)</volume><pubmed_abstract>&lt;h4>Aims&lt;/h4>To evaluate echocardiographic and biomarker changes during chemotherapy, assess their ability to early detect and predict cardiotoxicity and to define the best time for their evaluation.&lt;h4>Methods and results&lt;/h4>Seventy-two women with breast cancer (52 ± 9.8 years) treated with anthracyclines (26 also with trastuzumab), were evaluated for 14 months (6 echocardiograms/12 laboratory tests). We analysed: high-sensitivity cardiac troponin T, NT-proBNP, global longitudinal strain (GLS), left ventricle end-systolic volume (LVESV), left ventricle end-diastolic volume (LVEDV), and left ventricular ejection fraction (LVEF). Cardiotoxicity was defined as a reduction in LVEF>10% compared with baseline with LVEF&lt;53%. High-sensitivity troponin T levels rose gradually reaching a maximum p</pubmed_abstract><journal>ESC heart failure</journal><pubmed_title>Early detection of anthracycline- and trastuzumab-induced cardiotoxicity: value and optimal timing of serum biomarkers and echocardiographic parameters.</pubmed_title><pmcid>PMC8934964</pmcid><funding_grant_id>B2017/BMD‐3676</funding_grant_id><funding_grant_id>PI20/01238</funding_grant_id><funding_grant_id>PI15/02019</funding_grant_id><funding_grant_id>AORTASANA‐CM</funding_grant_id><pubmed_authors>Ramirez Merino N</pubmed_authors><pubmed_authors>Castellano JM</pubmed_authors><pubmed_authors>Moreno-Arciniegas A</pubmed_authors><pubmed_authors>Lopez-Melgar B</pubmed_authors><pubmed_authors>Madurga R</pubmed_authors><pubmed_authors>Parra Jimenez FJ</pubmed_authors><pubmed_authors>Ciruelos E</pubmed_authors><pubmed_authors>Martin-Asenjo R</pubmed_authors><pubmed_authors>Fernandez-Friera L</pubmed_authors><pubmed_authors>Solis J</pubmed_authors><pubmed_authors>Zorita B</pubmed_authors><pubmed_authors>Diaz-Anton B</pubmed_authors><pubmed_authors>Wasniewski S</pubmed_authors><pubmed_authors>Amado Escanuela MG</pubmed_authors><pubmed_authors>Barrio P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Early detection of anthracycline- and trastuzumab-induced cardiotoxicity: value and optimal timing of serum biomarkers and echocardiographic parameters.</name><description>&lt;h4>Aims&lt;/h4>To evaluate echocardiographic and biomarker changes during chemotherapy, assess their ability to early detect and predict cardiotoxicity and to define the best time for their evaluation.&lt;h4>Methods and results&lt;/h4>Seventy-two women with breast cancer (52 ± 9.8 years) treated with anthracyclines (26 also with trastuzumab), were evaluated for 14 months (6 echocardiograms/12 laboratory tests). We analysed: high-sensitivity cardiac troponin T, NT-proBNP, global longitudinal strain (GLS), left ventricle end-systolic volume (LVESV), left ventricle end-diastolic volume (LVEDV), and left ventricular ejection fraction (LVEF). Cardiotoxicity was defined as a reduction in LVEF>10% compared with baseline with LVEF&lt;53%. High-sensitivity troponin T levels rose gradually reaching a maximum p</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-26T04:39:57.111Z</modification><creation>2025-04-06T11:12:51.441Z</creation></dates><accession>S-EPMC8934964</accession><cross_references><pubmed>35106939</pubmed><doi>10.1002/ehf2.13782</doi></cross_references></HashMap>