Long-term follow-up assessment of cardiac safety in SAFE-HEaRt, a clinical trial evaluating the use of HER2-targeted therapies in patients with breast cancer and compromised heart function

Purpose HER2-targeted therapies are associated with cardiotoxicity which is usually asymptomatic and reversible. We report the updated cardiac safety assessment of patients with compromised heart function receiving HER2-targeted therapy for breast cancer, enrolled in the SAFE-HEaRt trial, at a media...

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Veröffentlicht in:Breast cancer research and treatment 2021-02, Vol.185 (3), p.863-868
Hauptverfasser: Khoury, Katia, Lynce, Filipa, Barac, Ana, Geng, Xue, Dang, Chau, Yu, Anthony F., Smith, Karen L., Gallagher, Christopher, Pohlmann, Paula R., Nunes, Raquel, Herbolsheimer, Pia, Warren, Robert, Srichai, Monvadi B., Hofmeyer, Mark, Asch, Federico, Tan, Ming, Isaacs, Claudine, Swain, Sandra M.
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container_end_page 868
container_issue 3
container_start_page 863
container_title Breast cancer research and treatment
container_volume 185
creator Khoury, Katia
Lynce, Filipa
Barac, Ana
Geng, Xue
Dang, Chau
Yu, Anthony F.
Smith, Karen L.
Gallagher, Christopher
Pohlmann, Paula R.
Nunes, Raquel
Herbolsheimer, Pia
Warren, Robert
Srichai, Monvadi B.
Hofmeyer, Mark
Asch, Federico
Tan, Ming
Isaacs, Claudine
Swain, Sandra M.
description Purpose HER2-targeted therapies are associated with cardiotoxicity which is usually asymptomatic and reversible. We report the updated cardiac safety assessment of patients with compromised heart function receiving HER2-targeted therapy for breast cancer, enrolled in the SAFE-HEaRt trial, at a median follow-up of 3.5 years. Methods Thirty patients with stage I-IV HER2-positive breast cancer receiving trastuzumab with or without pertuzumab, or ado-trastuzumab emtansine (T-DM1), with asymptomatic LVEF (left ventricular ejection fraction) 40–49%, were started on cardioprotective medications, with the primary endpoint being completion of HER2-targeted therapy without cardiac events (CE) or protocol-defined asymptomatic worsening of LVEF. IRB-approved follow-up assessment included 23 patients. Results Median follow-up as of June 2020 is 42 months. The study met its primary endpoint with 27 patients (90%) completing their HER2-targeted therapies without cardiac issues. Of the 23 evaluable patients at long-term f/u, 14 had early stage breast cancer, and 9 had metastatic disease, 8 of whom remained on HER2-targeted therapies. One patient developed symptomatic heart failure with no change in LVEF. There were no cardiac deaths. The mean LVEF improved to 52.1% from 44.9% at study baseline, including patients who remained on HER2-targeted therapy, and those who received prior anthracyclines. Conclusions Long-term follow-up of the SAFE-HEaRt study continues to provide safety data of HER2-targeted therapy use in patients with compromised heart function. The late development of cardiac dysfunction is uncommon and continued multi-disciplinary oncologic and cardiac care of patients is vital for improved patient outcomes.
doi_str_mv 10.1007/s10549-020-06053-y
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We report the updated cardiac safety assessment of patients with compromised heart function receiving HER2-targeted therapy for breast cancer, enrolled in the SAFE-HEaRt trial, at a median follow-up of 3.5 years. Methods Thirty patients with stage I-IV HER2-positive breast cancer receiving trastuzumab with or without pertuzumab, or ado-trastuzumab emtansine (T-DM1), with asymptomatic LVEF (left ventricular ejection fraction) 40–49%, were started on cardioprotective medications, with the primary endpoint being completion of HER2-targeted therapy without cardiac events (CE) or protocol-defined asymptomatic worsening of LVEF. IRB-approved follow-up assessment included 23 patients. Results Median follow-up as of June 2020 is 42 months. The study met its primary endpoint with 27 patients (90%) completing their HER2-targeted therapies without cardiac issues. Of the 23 evaluable patients at long-term f/u, 14 had early stage breast cancer, and 9 had metastatic disease, 8 of whom remained on HER2-targeted therapies. One patient developed symptomatic heart failure with no change in LVEF. There were no cardiac deaths. The mean LVEF improved to 52.1% from 44.9% at study baseline, including patients who remained on HER2-targeted therapy, and those who received prior anthracyclines. Conclusions Long-term follow-up of the SAFE-HEaRt study continues to provide safety data of HER2-targeted therapy use in patients with compromised heart function. The late development of cardiac dysfunction is uncommon and continued multi-disciplinary oncologic and cardiac care of patients is vital for improved patient outcomes.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-020-06053-y</identifier><identifier>PMID: 33400034</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Anthracycline ; Antineoplastic Combined Chemotherapy Protocols ; Asymptomatic ; Breast cancer ; Breast Neoplasms - complications ; Breast Neoplasms - drug therapy ; Brief Report ; Cancer ; Cancer patients ; Cancer research ; Cardiac patients ; Cardiotoxicity ; Care and treatment ; Clinical trials ; Congestive heart failure ; ErbB-2 protein ; Female ; Follow-Up Studies ; Health aspects ; Heart ; Humans ; Medical research ; Medicine ; Medicine &amp; Public Health ; Medicine, Experimental ; Metastases ; Metastasis ; Monoclonal antibodies ; Oncology ; Patients ; Pertuzumab ; Receptor, ErbB-2 - genetics ; Safety ; Stroke Volume ; Targeted cancer therapy ; Trastuzumab ; Trastuzumab - adverse effects ; Ventricle ; Ventricular Function, Left</subject><ispartof>Breast cancer research and treatment, 2021-02, Vol.185 (3), p.863-868</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature 2021</rights><rights>COPYRIGHT 2021 Springer</rights><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c572t-863023d54f2409042492e248616d82d2d82c17baa6e898f8588e48d345d951d63</citedby><cites>FETCH-LOGICAL-c572t-863023d54f2409042492e248616d82d2d82c17baa6e898f8588e48d345d951d63</cites><orcidid>0000-0002-1320-3830</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10549-020-06053-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10549-020-06053-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33400034$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Khoury, Katia</creatorcontrib><creatorcontrib>Lynce, Filipa</creatorcontrib><creatorcontrib>Barac, Ana</creatorcontrib><creatorcontrib>Geng, Xue</creatorcontrib><creatorcontrib>Dang, Chau</creatorcontrib><creatorcontrib>Yu, Anthony F.</creatorcontrib><creatorcontrib>Smith, Karen L.</creatorcontrib><creatorcontrib>Gallagher, Christopher</creatorcontrib><creatorcontrib>Pohlmann, Paula R.</creatorcontrib><creatorcontrib>Nunes, Raquel</creatorcontrib><creatorcontrib>Herbolsheimer, Pia</creatorcontrib><creatorcontrib>Warren, Robert</creatorcontrib><creatorcontrib>Srichai, Monvadi B.</creatorcontrib><creatorcontrib>Hofmeyer, Mark</creatorcontrib><creatorcontrib>Asch, Federico</creatorcontrib><creatorcontrib>Tan, Ming</creatorcontrib><creatorcontrib>Isaacs, Claudine</creatorcontrib><creatorcontrib>Swain, Sandra M.</creatorcontrib><title>Long-term follow-up assessment of cardiac safety in SAFE-HEaRt, a clinical trial evaluating the use of HER2-targeted therapies in patients with breast cancer and compromised heart function</title><title>Breast cancer research and treatment</title><addtitle>Breast Cancer Res Treat</addtitle><addtitle>Breast Cancer Res Treat</addtitle><description>Purpose HER2-targeted therapies are associated with cardiotoxicity which is usually asymptomatic and reversible. We report the updated cardiac safety assessment of patients with compromised heart function receiving HER2-targeted therapy for breast cancer, enrolled in the SAFE-HEaRt trial, at a median follow-up of 3.5 years. Methods Thirty patients with stage I-IV HER2-positive breast cancer receiving trastuzumab with or without pertuzumab, or ado-trastuzumab emtansine (T-DM1), with asymptomatic LVEF (left ventricular ejection fraction) 40–49%, were started on cardioprotective medications, with the primary endpoint being completion of HER2-targeted therapy without cardiac events (CE) or protocol-defined asymptomatic worsening of LVEF. IRB-approved follow-up assessment included 23 patients. Results Median follow-up as of June 2020 is 42 months. The study met its primary endpoint with 27 patients (90%) completing their HER2-targeted therapies without cardiac issues. Of the 23 evaluable patients at long-term f/u, 14 had early stage breast cancer, and 9 had metastatic disease, 8 of whom remained on HER2-targeted therapies. One patient developed symptomatic heart failure with no change in LVEF. There were no cardiac deaths. The mean LVEF improved to 52.1% from 44.9% at study baseline, including patients who remained on HER2-targeted therapy, and those who received prior anthracyclines. Conclusions Long-term follow-up of the SAFE-HEaRt study continues to provide safety data of HER2-targeted therapy use in patients with compromised heart function. The late development of cardiac dysfunction is uncommon and continued multi-disciplinary oncologic and cardiac care of patients is vital for improved patient outcomes.</description><subject>Anthracycline</subject><subject>Antineoplastic Combined Chemotherapy Protocols</subject><subject>Asymptomatic</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - complications</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Brief Report</subject><subject>Cancer</subject><subject>Cancer patients</subject><subject>Cancer research</subject><subject>Cardiac patients</subject><subject>Cardiotoxicity</subject><subject>Care and treatment</subject><subject>Clinical trials</subject><subject>Congestive heart failure</subject><subject>ErbB-2 protein</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Health aspects</subject><subject>Heart</subject><subject>Humans</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Medicine, Experimental</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Monoclonal antibodies</subject><subject>Oncology</subject><subject>Patients</subject><subject>Pertuzumab</subject><subject>Receptor, ErbB-2 - genetics</subject><subject>Safety</subject><subject>Stroke Volume</subject><subject>Targeted cancer therapy</subject><subject>Trastuzumab</subject><subject>Trastuzumab - adverse effects</subject><subject>Ventricle</subject><subject>Ventricular Function, Left</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9Ul1rFDEUHUSxtfoHfJCA0CdTM_mYybwIS9m6woJQ9TlkM3dmU2aSMcm07H_zx5l1a9sFkcANyT3n3A9OUbwtyUVJSP0xlkTwBhNKMKmIYHj3rDgtRc1wTcv6eXFKyqrGlSTVSfEqxhtCSFOT5mVxwhjPD8ZPi19r73qcIIyo88Pg7_A8IR0jxDiCS8h3yOjQWm1Q1B2kHbIOfVtcLfFqqa_TB6SRGayzRg8oBZsj3Oph1sm6HqUtoDnCXmS1vKY46dBDgnafCHqyEPdqUwbnUhHd2bRFmwA6plzUGQhIuxYZP07BjzZm4hZ0SKibnUnWu9fFi04PEd7c32fFj6vl98sVXn_9_OVyscZG1DRhWTFCWSt4RzlpCKe8oUC5rMqqlbSlOZiy3mhdgWxkJ4WUwGXLuGgbUbYVOys-HXSneTNCa3K3QQ9qCnbUYae8tuo44-xW9f5WSUpq2Ygs8P5eIPifM8SkbvwcXO5Z5WZ4XUrBySOq1wMo6zqfxUwe3KhFJZhgZSOajLr4ByqfFkZrvIPO5v8jwvkTQt7gkLbRD_N-g_EYSA9AE3yMAbqHCUui9o5TB8ep7Dj1x3Fql0nvnu7mgfLXYhnADoCYU66H8Dj7f2R_AyMS4iE</recordid><startdate>20210201</startdate><enddate>20210201</enddate><creator>Khoury, Katia</creator><creator>Lynce, Filipa</creator><creator>Barac, Ana</creator><creator>Geng, Xue</creator><creator>Dang, Chau</creator><creator>Yu, Anthony F.</creator><creator>Smith, Karen L.</creator><creator>Gallagher, Christopher</creator><creator>Pohlmann, Paula R.</creator><creator>Nunes, Raquel</creator><creator>Herbolsheimer, Pia</creator><creator>Warren, Robert</creator><creator>Srichai, Monvadi B.</creator><creator>Hofmeyer, Mark</creator><creator>Asch, Federico</creator><creator>Tan, Ming</creator><creator>Isaacs, Claudine</creator><creator>Swain, Sandra M.</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>K9-</scope><scope>K9.</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1320-3830</orcidid></search><sort><creationdate>20210201</creationdate><title>Long-term follow-up assessment of cardiac safety in SAFE-HEaRt, a clinical trial evaluating the use of HER2-targeted therapies in patients with breast cancer and compromised heart function</title><author>Khoury, Katia ; Lynce, Filipa ; Barac, Ana ; Geng, Xue ; Dang, Chau ; Yu, Anthony F. ; Smith, Karen L. ; Gallagher, Christopher ; Pohlmann, Paula R. ; Nunes, Raquel ; Herbolsheimer, Pia ; Warren, Robert ; Srichai, Monvadi B. ; Hofmeyer, Mark ; Asch, Federico ; Tan, Ming ; Isaacs, Claudine ; Swain, Sandra M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c572t-863023d54f2409042492e248616d82d2d82c17baa6e898f8588e48d345d951d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anthracycline</topic><topic>Antineoplastic Combined Chemotherapy Protocols</topic><topic>Asymptomatic</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - complications</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Brief Report</topic><topic>Cancer</topic><topic>Cancer patients</topic><topic>Cancer research</topic><topic>Cardiac patients</topic><topic>Cardiotoxicity</topic><topic>Care and treatment</topic><topic>Clinical trials</topic><topic>Congestive heart failure</topic><topic>ErbB-2 protein</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Health aspects</topic><topic>Heart</topic><topic>Humans</topic><topic>Medical research</topic><topic>Medicine</topic><topic>Medicine &amp; 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We report the updated cardiac safety assessment of patients with compromised heart function receiving HER2-targeted therapy for breast cancer, enrolled in the SAFE-HEaRt trial, at a median follow-up of 3.5 years. Methods Thirty patients with stage I-IV HER2-positive breast cancer receiving trastuzumab with or without pertuzumab, or ado-trastuzumab emtansine (T-DM1), with asymptomatic LVEF (left ventricular ejection fraction) 40–49%, were started on cardioprotective medications, with the primary endpoint being completion of HER2-targeted therapy without cardiac events (CE) or protocol-defined asymptomatic worsening of LVEF. IRB-approved follow-up assessment included 23 patients. Results Median follow-up as of June 2020 is 42 months. The study met its primary endpoint with 27 patients (90%) completing their HER2-targeted therapies without cardiac issues. Of the 23 evaluable patients at long-term f/u, 14 had early stage breast cancer, and 9 had metastatic disease, 8 of whom remained on HER2-targeted therapies. One patient developed symptomatic heart failure with no change in LVEF. There were no cardiac deaths. The mean LVEF improved to 52.1% from 44.9% at study baseline, including patients who remained on HER2-targeted therapy, and those who received prior anthracyclines. Conclusions Long-term follow-up of the SAFE-HEaRt study continues to provide safety data of HER2-targeted therapy use in patients with compromised heart function. The late development of cardiac dysfunction is uncommon and continued multi-disciplinary oncologic and cardiac care of patients is vital for improved patient outcomes.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>33400034</pmid><doi>10.1007/s10549-020-06053-y</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-1320-3830</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Anthracycline
Antineoplastic Combined Chemotherapy Protocols
Asymptomatic
Breast cancer
Breast Neoplasms - complications
Breast Neoplasms - drug therapy
Brief Report
Cancer
Cancer patients
Cancer research
Cardiac patients
Cardiotoxicity
Care and treatment
Clinical trials
Congestive heart failure
ErbB-2 protein
Female
Follow-Up Studies
Health aspects
Heart
Humans
Medical research
Medicine
Medicine & Public Health
Medicine, Experimental
Metastases
Metastasis
Monoclonal antibodies
Oncology
Patients
Pertuzumab
Receptor, ErbB-2 - genetics
Safety
Stroke Volume
Targeted cancer therapy
Trastuzumab
Trastuzumab - adverse effects
Ventricle
Ventricular Function, Left
title Long-term follow-up assessment of cardiac safety in SAFE-HEaRt, a clinical trial evaluating the use of HER2-targeted therapies in patients with breast cancer and compromised heart function
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