Prospective evaluation of the cardiac safety of HER2-targeted therapies in patients with HER2-positive breast cancer and compromised heart function: the SAFE-HEaRt study

Purpose HER2-targeted therapies have substantially improved the outcome of patients with breast cancer, however, they can be associated with cardiac toxicity. Guidelines recommend holding HER2-targeted therapies until resolution of cardiac dysfunction. SAFE-HEaRt is the first trial that prospectivel...

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Veröffentlicht in:Breast cancer research and treatment 2019-06, Vol.175 (3), p.595-603
Hauptverfasser: Lynce, F., Barac, A., Geng, X., Dang, C., Yu, A. F., Smith, K. L., Gallagher, C., Pohlmann, P. R., Nunes, R., Herbolsheimer, P., Warren, R., Srichai, M. B., Hofmeyer, M., Cunningham, A., Timothee, P., Asch, F. M., Shajahan-Haq, A., Tan, M. T., Isaacs, C., Swain, S. M.
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container_end_page 603
container_issue 3
container_start_page 595
container_title Breast cancer research and treatment
container_volume 175
creator Lynce, F.
Barac, A.
Geng, X.
Dang, C.
Yu, A. F.
Smith, K. L.
Gallagher, C.
Pohlmann, P. R.
Nunes, R.
Herbolsheimer, P.
Warren, R.
Srichai, M. B.
Hofmeyer, M.
Cunningham, A.
Timothee, P.
Asch, F. M.
Shajahan-Haq, A.
Tan, M. T.
Isaacs, C.
Swain, S. M.
description Purpose HER2-targeted therapies have substantially improved the outcome of patients with breast cancer, however, they can be associated with cardiac toxicity. Guidelines recommend holding HER2-targeted therapies until resolution of cardiac dysfunction. SAFE-HEaRt is the first trial that prospectively tests whether these therapies can be safely administered without interruptions in patients with cardiac dysfunction. Methods Patients with stage I–IV HER2-positive breast cancer candidates for trastuzumab, pertuzumab or ado-trastuzumab emtansine (TDM-1), with left ventricular ejection fraction (LVEF) 40–49% and no symptoms of heart failure (HF) were enrolled. All patients underwent cardiology visits, serial echocardiograms and received beta blockers and ACE inhibitors unless contraindicated. The primary endpoint was completion of the planned HER2-targeted therapies without developing either a cardiac event (CE) defined as HF, myocardial infarction, arrhythmia or cardiac death or significant asymptomatic worsening of LVEF. The study was considered successful if planned oncology therapy completion rate was at least 30%. Results Of 31 enrolled patients, 30 were evaluable. Fifteen patients were treated with trastuzumab, 14 with trastuzumab and pertuzumab, and 2 with TDM-1. Mean LVEF was 45% at baseline and 46% at the end of treatment. Twenty-seven patients (90%) completed the planned HER2-targeted therapies. Two patients experienced a CE and 1 had an asymptomatic worsening of LVEF to ≤ 35%. Conclusion This study provides safety data of HER2-targeted therapies in patients with breast cancer and reduced LVEF while receiving cardioprotective medications and close cardiac monitoring. Our results demonstrate the importance of collaboration between cardiology and oncology providers to allow for delivery of optimal oncologic care to this unique population.
doi_str_mv 10.1007/s10549-019-05191-2
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F. ; Smith, K. L. ; Gallagher, C. ; Pohlmann, P. R. ; Nunes, R. ; Herbolsheimer, P. ; Warren, R. ; Srichai, M. B. ; Hofmeyer, M. ; Cunningham, A. ; Timothee, P. ; Asch, F. M. ; Shajahan-Haq, A. ; Tan, M. T. ; Isaacs, C. ; Swain, S. M.</creator><creatorcontrib>Lynce, F. ; Barac, A. ; Geng, X. ; Dang, C. ; Yu, A. F. ; Smith, K. L. ; Gallagher, C. ; Pohlmann, P. R. ; Nunes, R. ; Herbolsheimer, P. ; Warren, R. ; Srichai, M. B. ; Hofmeyer, M. ; Cunningham, A. ; Timothee, P. ; Asch, F. M. ; Shajahan-Haq, A. ; Tan, M. T. ; Isaacs, C. ; Swain, S. M.</creatorcontrib><description>Purpose HER2-targeted therapies have substantially improved the outcome of patients with breast cancer, however, they can be associated with cardiac toxicity. Guidelines recommend holding HER2-targeted therapies until resolution of cardiac dysfunction. SAFE-HEaRt is the first trial that prospectively tests whether these therapies can be safely administered without interruptions in patients with cardiac dysfunction. Methods Patients with stage I–IV HER2-positive breast cancer candidates for trastuzumab, pertuzumab or ado-trastuzumab emtansine (TDM-1), with left ventricular ejection fraction (LVEF) 40–49% and no symptoms of heart failure (HF) were enrolled. All patients underwent cardiology visits, serial echocardiograms and received beta blockers and ACE inhibitors unless contraindicated. The primary endpoint was completion of the planned HER2-targeted therapies without developing either a cardiac event (CE) defined as HF, myocardial infarction, arrhythmia or cardiac death or significant asymptomatic worsening of LVEF. The study was considered successful if planned oncology therapy completion rate was at least 30%. Results Of 31 enrolled patients, 30 were evaluable. Fifteen patients were treated with trastuzumab, 14 with trastuzumab and pertuzumab, and 2 with TDM-1. Mean LVEF was 45% at baseline and 46% at the end of treatment. Twenty-seven patients (90%) completed the planned HER2-targeted therapies. Two patients experienced a CE and 1 had an asymptomatic worsening of LVEF to ≤ 35%. Conclusion This study provides safety data of HER2-targeted therapies in patients with breast cancer and reduced LVEF while receiving cardioprotective medications and close cardiac monitoring. Our results demonstrate the importance of collaboration between cardiology and oncology providers to allow for delivery of optimal oncologic care to this unique population.</description><identifier>ISSN: 0167-6806</identifier><identifier>EISSN: 1573-7217</identifier><identifier>DOI: 10.1007/s10549-019-05191-2</identifier><identifier>PMID: 30852761</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Ado-Trastuzumab Emtansine ; Adrenergic beta blockers ; Adrenergic beta-Antagonists - therapeutic use ; Adult ; Aged ; Angiotensin-Converting Enzyme Inhibitors - therapeutic use ; Antibodies, Monoclonal, Humanized - administration &amp; dosage ; Antibodies, Monoclonal, Humanized - adverse effects ; Arrhythmia ; Breast cancer ; Breast Neoplasms - drug therapy ; Breast Neoplasms - metabolism ; Cancer ; Cancer patients ; Cancer research ; Cardiac patients ; Cardiology ; Care and treatment ; Clinical Trial ; Congestive heart failure ; ErbB-2 protein ; Female ; Heart ; Heart attack ; Humans ; Maytansine - administration &amp; dosage ; Maytansine - adverse effects ; Maytansine - analogs &amp; derivatives ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Molecular Targeted Therapy - adverse effects ; Monoclonal antibodies ; Myocardial infarction ; Neoplasm Staging ; Oncology ; Oncology, Experimental ; Patients ; Pertuzumab ; Pilot Projects ; Prospective Studies ; Receptor, ErbB-2 - metabolism ; Targeted cancer therapy ; Toxicity ; Trastuzumab ; Trastuzumab - administration &amp; dosage ; Trastuzumab - adverse effects ; Treatment Outcome ; Ventricle ; Ventricular Dysfunction, Left - chemically induced ; Ventricular Dysfunction, Left - drug therapy ; Ventricular Dysfunction, Left - physiopathology</subject><ispartof>Breast cancer research and treatment, 2019-06, Vol.175 (3), p.595-603</ispartof><rights>The Author(s) 2019</rights><rights>COPYRIGHT 2019 Springer</rights><rights>Breast Cancer Research and Treatment is a copyright of Springer, (2019). All Rights Reserved. © 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c572t-8d07f97936285d3ad41ece48b5dfcf00d51cffb961f6c5d58a8c30a88f7764df3</citedby><cites>FETCH-LOGICAL-c572t-8d07f97936285d3ad41ece48b5dfcf00d51cffb961f6c5d58a8c30a88f7764df3</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/s10549-019-05191-2$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10549-019-05191-2$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30852761$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lynce, F.</creatorcontrib><creatorcontrib>Barac, A.</creatorcontrib><creatorcontrib>Geng, X.</creatorcontrib><creatorcontrib>Dang, C.</creatorcontrib><creatorcontrib>Yu, A. F.</creatorcontrib><creatorcontrib>Smith, K. L.</creatorcontrib><creatorcontrib>Gallagher, C.</creatorcontrib><creatorcontrib>Pohlmann, P. R.</creatorcontrib><creatorcontrib>Nunes, R.</creatorcontrib><creatorcontrib>Herbolsheimer, P.</creatorcontrib><creatorcontrib>Warren, R.</creatorcontrib><creatorcontrib>Srichai, M. B.</creatorcontrib><creatorcontrib>Hofmeyer, M.</creatorcontrib><creatorcontrib>Cunningham, A.</creatorcontrib><creatorcontrib>Timothee, P.</creatorcontrib><creatorcontrib>Asch, F. M.</creatorcontrib><creatorcontrib>Shajahan-Haq, A.</creatorcontrib><creatorcontrib>Tan, M. T.</creatorcontrib><creatorcontrib>Isaacs, C.</creatorcontrib><creatorcontrib>Swain, S. M.</creatorcontrib><title>Prospective evaluation of the cardiac safety of HER2-targeted therapies in patients with HER2-positive breast cancer and compromised heart function: the SAFE-HEaRt study</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 have substantially improved the outcome of patients with breast cancer, however, they can be associated with cardiac toxicity. Guidelines recommend holding HER2-targeted therapies until resolution of cardiac dysfunction. SAFE-HEaRt is the first trial that prospectively tests whether these therapies can be safely administered without interruptions in patients with cardiac dysfunction. Methods Patients with stage I–IV HER2-positive breast cancer candidates for trastuzumab, pertuzumab or ado-trastuzumab emtansine (TDM-1), with left ventricular ejection fraction (LVEF) 40–49% and no symptoms of heart failure (HF) were enrolled. All patients underwent cardiology visits, serial echocardiograms and received beta blockers and ACE inhibitors unless contraindicated. The primary endpoint was completion of the planned HER2-targeted therapies without developing either a cardiac event (CE) defined as HF, myocardial infarction, arrhythmia or cardiac death or significant asymptomatic worsening of LVEF. The study was considered successful if planned oncology therapy completion rate was at least 30%. Results Of 31 enrolled patients, 30 were evaluable. Fifteen patients were treated with trastuzumab, 14 with trastuzumab and pertuzumab, and 2 with TDM-1. Mean LVEF was 45% at baseline and 46% at the end of treatment. Twenty-seven patients (90%) completed the planned HER2-targeted therapies. Two patients experienced a CE and 1 had an asymptomatic worsening of LVEF to ≤ 35%. Conclusion This study provides safety data of HER2-targeted therapies in patients with breast cancer and reduced LVEF while receiving cardioprotective medications and close cardiac monitoring. Our results demonstrate the importance of collaboration between cardiology and oncology providers to allow for delivery of optimal oncologic care to this unique population.</description><subject>Ado-Trastuzumab Emtansine</subject><subject>Adrenergic beta blockers</subject><subject>Adrenergic beta-Antagonists - therapeutic use</subject><subject>Adult</subject><subject>Aged</subject><subject>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</subject><subject>Antibodies, Monoclonal, Humanized - administration &amp; dosage</subject><subject>Antibodies, Monoclonal, Humanized - adverse effects</subject><subject>Arrhythmia</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - metabolism</subject><subject>Cancer</subject><subject>Cancer patients</subject><subject>Cancer research</subject><subject>Cardiac patients</subject><subject>Cardiology</subject><subject>Care and treatment</subject><subject>Clinical Trial</subject><subject>Congestive heart failure</subject><subject>ErbB-2 protein</subject><subject>Female</subject><subject>Heart</subject><subject>Heart attack</subject><subject>Humans</subject><subject>Maytansine - administration &amp; dosage</subject><subject>Maytansine - adverse effects</subject><subject>Maytansine - analogs &amp; derivatives</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Molecular Targeted Therapy - adverse effects</subject><subject>Monoclonal antibodies</subject><subject>Myocardial infarction</subject><subject>Neoplasm Staging</subject><subject>Oncology</subject><subject>Oncology, Experimental</subject><subject>Patients</subject><subject>Pertuzumab</subject><subject>Pilot Projects</subject><subject>Prospective Studies</subject><subject>Receptor, ErbB-2 - metabolism</subject><subject>Targeted cancer therapy</subject><subject>Toxicity</subject><subject>Trastuzumab</subject><subject>Trastuzumab - administration &amp; dosage</subject><subject>Trastuzumab - adverse effects</subject><subject>Treatment Outcome</subject><subject>Ventricle</subject><subject>Ventricular Dysfunction, Left - chemically induced</subject><subject>Ventricular Dysfunction, Left - drug therapy</subject><subject>Ventricular Dysfunction, Left - physiopathology</subject><issn>0167-6806</issn><issn>1573-7217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kl2LEzEUhgdR3Lr6B7yQgODdrElm8jFeCGXpWmFBWfU6pPlos0yTMclU-pP8l6addXcLIiEEkvd9Ts7hrarXCF4gCNn7hCBpuxqisgnqUI2fVDNEWFMzjNjTagYRZTXlkJ5VL1K6hRB2DHbPq7MGcoIZRbPq99cY0mBUdjsDzE72o8wueBAsyBsDlIzaSQWStCbvD7fLxQ2us4xrk40-aKIcnEnAeTAUq_E5gV8ubybhEJI7olfRyJQLzysTgfQaqLAdYti6VDAbI2MGdvTqUPzDsfS3-dWiXi7kTQYpj3r_snpmZZ_Mq7vzvPpxtfh-uayvv3z6fDm_rhVhONdcQ2Y71jUUc6IbqVtklGn5imirLISaIGXtqqPIUkU04ZKrBkrOLWO01bY5rz5O3GFcbY1WpaMoezFEt5VxL4J04vTFu41Yh52gpGkJagrg7R0ghp-jSVnchjH68meBEe9w2_AWPqjWsjfCeRsKTJVxKDEnnFJMJ9bFP1RlabN1KnhjXbk_Mbx7ZChz7fMmhX48zDWdCvEkVCUAKRp73yGC4hAvMcVLlHiJY7wELqY3j2dzb_mbpyJoJkEqT35t4kPv_8H-AV8t3II</recordid><startdate>20190601</startdate><enddate>20190601</enddate><creator>Lynce, F.</creator><creator>Barac, A.</creator><creator>Geng, X.</creator><creator>Dang, C.</creator><creator>Yu, A. 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F.</au><au>Smith, K. L.</au><au>Gallagher, C.</au><au>Pohlmann, P. R.</au><au>Nunes, R.</au><au>Herbolsheimer, P.</au><au>Warren, R.</au><au>Srichai, M. B.</au><au>Hofmeyer, M.</au><au>Cunningham, A.</au><au>Timothee, P.</au><au>Asch, F. M.</au><au>Shajahan-Haq, A.</au><au>Tan, M. T.</au><au>Isaacs, C.</au><au>Swain, S. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prospective evaluation of the cardiac safety of HER2-targeted therapies in patients with HER2-positive breast cancer and compromised heart function: the SAFE-HEaRt study</atitle><jtitle>Breast cancer research and treatment</jtitle><stitle>Breast Cancer Res Treat</stitle><addtitle>Breast Cancer Res Treat</addtitle><date>2019-06-01</date><risdate>2019</risdate><volume>175</volume><issue>3</issue><spage>595</spage><epage>603</epage><pages>595-603</pages><issn>0167-6806</issn><eissn>1573-7217</eissn><abstract>Purpose HER2-targeted therapies have substantially improved the outcome of patients with breast cancer, however, they can be associated with cardiac toxicity. Guidelines recommend holding HER2-targeted therapies until resolution of cardiac dysfunction. SAFE-HEaRt is the first trial that prospectively tests whether these therapies can be safely administered without interruptions in patients with cardiac dysfunction. Methods Patients with stage I–IV HER2-positive breast cancer candidates for trastuzumab, pertuzumab or ado-trastuzumab emtansine (TDM-1), with left ventricular ejection fraction (LVEF) 40–49% and no symptoms of heart failure (HF) were enrolled. All patients underwent cardiology visits, serial echocardiograms and received beta blockers and ACE inhibitors unless contraindicated. The primary endpoint was completion of the planned HER2-targeted therapies without developing either a cardiac event (CE) defined as HF, myocardial infarction, arrhythmia or cardiac death or significant asymptomatic worsening of LVEF. The study was considered successful if planned oncology therapy completion rate was at least 30%. Results Of 31 enrolled patients, 30 were evaluable. Fifteen patients were treated with trastuzumab, 14 with trastuzumab and pertuzumab, and 2 with TDM-1. Mean LVEF was 45% at baseline and 46% at the end of treatment. Twenty-seven patients (90%) completed the planned HER2-targeted therapies. Two patients experienced a CE and 1 had an asymptomatic worsening of LVEF to ≤ 35%. Conclusion This study provides safety data of HER2-targeted therapies in patients with breast cancer and reduced LVEF while receiving cardioprotective medications and close cardiac monitoring. Our results demonstrate the importance of collaboration between cardiology and oncology providers to allow for delivery of optimal oncologic care to this unique population.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>30852761</pmid><doi>10.1007/s10549-019-05191-2</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-1320-3830</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0167-6806
ispartof Breast cancer research and treatment, 2019-06, Vol.175 (3), p.595-603
issn 0167-6806
1573-7217
language eng
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source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Ado-Trastuzumab Emtansine
Adrenergic beta blockers
Adrenergic beta-Antagonists - therapeutic use
Adult
Aged
Angiotensin-Converting Enzyme Inhibitors - therapeutic use
Antibodies, Monoclonal, Humanized - administration & dosage
Antibodies, Monoclonal, Humanized - adverse effects
Arrhythmia
Breast cancer
Breast Neoplasms - drug therapy
Breast Neoplasms - metabolism
Cancer
Cancer patients
Cancer research
Cardiac patients
Cardiology
Care and treatment
Clinical Trial
Congestive heart failure
ErbB-2 protein
Female
Heart
Heart attack
Humans
Maytansine - administration & dosage
Maytansine - adverse effects
Maytansine - analogs & derivatives
Medicine
Medicine & Public Health
Middle Aged
Molecular Targeted Therapy - adverse effects
Monoclonal antibodies
Myocardial infarction
Neoplasm Staging
Oncology
Oncology, Experimental
Patients
Pertuzumab
Pilot Projects
Prospective Studies
Receptor, ErbB-2 - metabolism
Targeted cancer therapy
Toxicity
Trastuzumab
Trastuzumab - administration & dosage
Trastuzumab - adverse effects
Treatment Outcome
Ventricle
Ventricular Dysfunction, Left - chemically induced
Ventricular Dysfunction, Left - drug therapy
Ventricular Dysfunction, Left - physiopathology
title Prospective evaluation of the cardiac safety of HER2-targeted therapies in patients with HER2-positive breast cancer and compromised heart function: the SAFE-HEaRt study
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