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 |
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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 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6534513</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A586626513</galeid><sourcerecordid>A586626513</sourcerecordid><originalsourceid>FETCH-LOGICAL-c572t-8d07f97936285d3ad41ece48b5dfcf00d51cffb961f6c5d58a8c30a88f7764df3</originalsourceid><addsrcrecordid>eNp9kl2LEzEUhgdR3Lr6B7yQgODdrElm8jFeCGXpWmFBWfU6pPlos0yTMclU-pP8l6addXcLIiEEkvd9Ts7hrarXCF4gCNn7hCBpuxqisgnqUI2fVDNEWFMzjNjTagYRZTXlkJ5VL1K6hRB2DHbPq7MGcoIZRbPq99cY0mBUdjsDzE72o8wueBAsyBsDlIzaSQWStCbvD7fLxQ2us4xrk40-aKIcnEnAeTAUq_E5gV8ubybhEJI7olfRyJQLzysTgfQaqLAdYti6VDAbI2MGdvTqUPzDsfS3-dWiXi7kTQYpj3r_snpmZZ_Mq7vzvPpxtfh-uayvv3z6fDm_rhVhONdcQ2Y71jUUc6IbqVtklGn5imirLISaIGXtqqPIUkU04ZKrBkrOLWO01bY5rz5O3GFcbY1WpaMoezFEt5VxL4J04vTFu41Yh52gpGkJagrg7R0ghp-jSVnchjH68meBEe9w2_AWPqjWsjfCeRsKTJVxKDEnnFJMJ9bFP1RlabN1KnhjXbk_Mbx7ZChz7fMmhX48zDWdCvEkVCUAKRp73yGC4hAvMcVLlHiJY7wELqY3j2dzb_mbpyJoJkEqT35t4kPv_8H-AV8t3II</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2189243840</pqid></control><display><type>article</type><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><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><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.</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 & 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</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 & 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 & dosage</subject><subject>Maytansine - adverse effects</subject><subject>Maytansine - analogs & derivatives</subject><subject>Medicine</subject><subject>Medicine & 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 & 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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M.</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>C6C</scope><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>20190601</creationdate><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><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c572t-8d07f97936285d3ad41ece48b5dfcf00d51cffb961f6c5d58a8c30a88f7764df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Ado-Trastuzumab Emtansine</topic><topic>Adrenergic beta blockers</topic><topic>Adrenergic beta-Antagonists - therapeutic use</topic><topic>Adult</topic><topic>Aged</topic><topic>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</topic><topic>Antibodies, Monoclonal, Humanized - administration & dosage</topic><topic>Antibodies, Monoclonal, Humanized - adverse effects</topic><topic>Arrhythmia</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - metabolism</topic><topic>Cancer</topic><topic>Cancer patients</topic><topic>Cancer research</topic><topic>Cardiac patients</topic><topic>Cardiology</topic><topic>Care and treatment</topic><topic>Clinical Trial</topic><topic>Congestive heart failure</topic><topic>ErbB-2 protein</topic><topic>Female</topic><topic>Heart</topic><topic>Heart attack</topic><topic>Humans</topic><topic>Maytansine - administration & dosage</topic><topic>Maytansine - adverse effects</topic><topic>Maytansine - analogs & derivatives</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Molecular Targeted Therapy - adverse effects</topic><topic>Monoclonal antibodies</topic><topic>Myocardial infarction</topic><topic>Neoplasm Staging</topic><topic>Oncology</topic><topic>Oncology, Experimental</topic><topic>Patients</topic><topic>Pertuzumab</topic><topic>Pilot Projects</topic><topic>Prospective Studies</topic><topic>Receptor, ErbB-2 - metabolism</topic><topic>Targeted cancer therapy</topic><topic>Toxicity</topic><topic>Trastuzumab</topic><topic>Trastuzumab - administration & dosage</topic><topic>Trastuzumab - adverse effects</topic><topic>Treatment Outcome</topic><topic>Ventricle</topic><topic>Ventricular Dysfunction, Left - chemically induced</topic><topic>Ventricular Dysfunction, Left - drug therapy</topic><topic>Ventricular Dysfunction, Left - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lynce, F.</creatorcontrib><creatorcontrib>Barac, A.</creatorcontrib><creatorcontrib>Geng, X.</creatorcontrib><creatorcontrib>Dang, C.</creatorcontrib><creatorcontrib>Yu, A. 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M.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Breast cancer research and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lynce, F.</au><au>Barac, A.</au><au>Geng, X.</au><au>Dang, C.</au><au>Yu, A. 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> |
fulltext | fulltext |
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 |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6534513 |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T18%3A18%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Prospective%20evaluation%20of%20the%20cardiac%20safety%20of%20HER2-targeted%20therapies%20in%20patients%20with%20HER2-positive%20breast%20cancer%20and%20compromised%20heart%20function:%20the%20SAFE-HEaRt%20study&rft.jtitle=Breast%20cancer%20research%20and%20treatment&rft.au=Lynce,%20F.&rft.date=2019-06-01&rft.volume=175&rft.issue=3&rft.spage=595&rft.epage=603&rft.pages=595-603&rft.issn=0167-6806&rft.eissn=1573-7217&rft_id=info:doi/10.1007/s10549-019-05191-2&rft_dat=%3Cgale_pubme%3EA586626513%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2189243840&rft_id=info:pmid/30852761&rft_galeid=A586626513&rfr_iscdi=true |