Management of cardiac toxicity in patients receiving vascular endothelial growth factor signaling pathway inhibitors
Background Interfering with angiogenesis is an effective, widely used approach to cancer therapy, but antiangiogenic therapies have been associated with important systemic cardiovascular toxicities such as hypertension, left ventricular dysfunction, heart failure, and myocardial ischemia and infarct...
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Veröffentlicht in: | The American heart journal 2012-02, Vol.163 (2), p.156-163 |
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creator | Steingart, Richard M., MD Bakris, George L., MD Chen, Helen X., MD Chen, Ming-Hui, MD, MMSc Force, Thomas, MD Ivy, S. Percy, MD Leier, Carl V., MD Liu, Glenn, MD Lenihan, Daniel, MD Lindenfeld, JoAnn, MD Maitland, Michael L., MD, PhD Remick, Scot C., MD Tang, W.H. Wilson, MD |
description | Background Interfering with angiogenesis is an effective, widely used approach to cancer therapy, but antiangiogenic therapies have been associated with important systemic cardiovascular toxicities such as hypertension, left ventricular dysfunction, heart failure, and myocardial ischemia and infarction. As the use of vascular endothelial growth factor signaling pathway (VSP) inhibitors broadens to include older patients and those with existing cardiovascular disease, the adverse effects are likely to be more frequent, and cardiologists will increasingly be enlisted to help oncologists manage patients who develop adverse cardiovascular effects. Methods The Cardiovascular Toxicities Panel of the National Cancer Institute reviewed the published literature and abstracts from major meetings, shared experience gained during clinical development of VSP inhibitors, and contributed extensive clinical experience in evaluating and treating patients with cancer with cardiovascular disease. This report was edited and approved by the National Cancer Institute Investigational Drug Steering Committee. It presents the panel's expert opinion on the current clinical use and future investigation for safer, more expansive use of these drugs. Results and Conclusions The panel recommends that physicians (1) conduct and document a formal risk assessment for existing cardiovascular disease and potential cardiovascular complications before VSP inhibitor treatment recognizing that preexisting hypertension and cardiovascular disease are common in patients with cancer, (2) actively monitor for blood pressure elevations and cardiac toxicity with more frequent assessments during the first treatment cycle, and (3) aggressively manage blood pressure elevations and early symptoms and signs of cardiac toxicity to prevent clinically limiting complications of VSP inhibitor therapy. |
doi_str_mv | 10.1016/j.ahj.2011.10.018 |
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Percy, MD ; Leier, Carl V., MD ; Liu, Glenn, MD ; Lenihan, Daniel, MD ; Lindenfeld, JoAnn, MD ; Maitland, Michael L., MD, PhD ; Remick, Scot C., MD ; Tang, W.H. Wilson, MD</creator><creatorcontrib>Steingart, Richard M., MD ; Bakris, George L., MD ; Chen, Helen X., MD ; Chen, Ming-Hui, MD, MMSc ; Force, Thomas, MD ; Ivy, S. Percy, MD ; Leier, Carl V., MD ; Liu, Glenn, MD ; Lenihan, Daniel, MD ; Lindenfeld, JoAnn, MD ; Maitland, Michael L., MD, PhD ; Remick, Scot C., MD ; Tang, W.H. Wilson, MD</creatorcontrib><description>Background Interfering with angiogenesis is an effective, widely used approach to cancer therapy, but antiangiogenic therapies have been associated with important systemic cardiovascular toxicities such as hypertension, left ventricular dysfunction, heart failure, and myocardial ischemia and infarction. As the use of vascular endothelial growth factor signaling pathway (VSP) inhibitors broadens to include older patients and those with existing cardiovascular disease, the adverse effects are likely to be more frequent, and cardiologists will increasingly be enlisted to help oncologists manage patients who develop adverse cardiovascular effects. Methods The Cardiovascular Toxicities Panel of the National Cancer Institute reviewed the published literature and abstracts from major meetings, shared experience gained during clinical development of VSP inhibitors, and contributed extensive clinical experience in evaluating and treating patients with cancer with cardiovascular disease. This report was edited and approved by the National Cancer Institute Investigational Drug Steering Committee. It presents the panel's expert opinion on the current clinical use and future investigation for safer, more expansive use of these drugs. Results and Conclusions The panel recommends that physicians (1) conduct and document a formal risk assessment for existing cardiovascular disease and potential cardiovascular complications before VSP inhibitor treatment recognizing that preexisting hypertension and cardiovascular disease are common in patients with cancer, (2) actively monitor for blood pressure elevations and cardiac toxicity with more frequent assessments during the first treatment cycle, and (3) aggressively manage blood pressure elevations and early symptoms and signs of cardiac toxicity to prevent clinically limiting complications of VSP inhibitor therapy.</description><identifier>ISSN: 0002-8703</identifier><identifier>EISSN: 1097-6744</identifier><identifier>DOI: 10.1016/j.ahj.2011.10.018</identifier><identifier>PMID: 22305831</identifier><identifier>CODEN: AHJOA2</identifier><language>eng</language><publisher>New York, NY: Mosby, Inc</publisher><subject>Antineoplastic Agents - adverse effects ; Antineoplastic Agents - therapeutic use ; Biological and medical sciences ; Cancer therapies ; Cardiology. Vascular system ; Cardiovascular ; Cardiovascular Diseases - chemically induced ; Cardiovascular Diseases - epidemiology ; Cardiovascular Diseases - prevention & control ; Cardiovascular System - drug effects ; Cholesterol ; Disease Management ; Drug therapy ; Epidermal Growth Factor - antagonists & inhibitors ; Global Health ; Heart attacks ; Humans ; Incidence ; Kinases ; Medical sciences ; Neoplasms - drug therapy ; Risk Factors ; Signal Transduction - drug effects ; Vascular endothelial growth factor</subject><ispartof>The American heart journal, 2012-02, Vol.163 (2), p.156-163</ispartof><rights>Mosby, Inc.</rights><rights>2012 Mosby, Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 Mosby, Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Feb 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c564t-57f6446264139047d072f4ee58b7b998787525df804d423ba425c959893c0f153</citedby><cites>FETCH-LOGICAL-c564t-57f6446264139047d072f4ee58b7b998787525df804d423ba425c959893c0f153</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0002870311007782$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25963694$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22305831$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Steingart, Richard M., MD</creatorcontrib><creatorcontrib>Bakris, George L., MD</creatorcontrib><creatorcontrib>Chen, Helen X., MD</creatorcontrib><creatorcontrib>Chen, Ming-Hui, MD, MMSc</creatorcontrib><creatorcontrib>Force, Thomas, MD</creatorcontrib><creatorcontrib>Ivy, S. Percy, MD</creatorcontrib><creatorcontrib>Leier, Carl V., MD</creatorcontrib><creatorcontrib>Liu, Glenn, MD</creatorcontrib><creatorcontrib>Lenihan, Daniel, MD</creatorcontrib><creatorcontrib>Lindenfeld, JoAnn, MD</creatorcontrib><creatorcontrib>Maitland, Michael L., MD, PhD</creatorcontrib><creatorcontrib>Remick, Scot C., MD</creatorcontrib><creatorcontrib>Tang, W.H. Wilson, MD</creatorcontrib><title>Management of cardiac toxicity in patients receiving vascular endothelial growth factor signaling pathway inhibitors</title><title>The American heart journal</title><addtitle>Am Heart J</addtitle><description>Background Interfering with angiogenesis is an effective, widely used approach to cancer therapy, but antiangiogenic therapies have been associated with important systemic cardiovascular toxicities such as hypertension, left ventricular dysfunction, heart failure, and myocardial ischemia and infarction. As the use of vascular endothelial growth factor signaling pathway (VSP) inhibitors broadens to include older patients and those with existing cardiovascular disease, the adverse effects are likely to be more frequent, and cardiologists will increasingly be enlisted to help oncologists manage patients who develop adverse cardiovascular effects. Methods The Cardiovascular Toxicities Panel of the National Cancer Institute reviewed the published literature and abstracts from major meetings, shared experience gained during clinical development of VSP inhibitors, and contributed extensive clinical experience in evaluating and treating patients with cancer with cardiovascular disease. This report was edited and approved by the National Cancer Institute Investigational Drug Steering Committee. It presents the panel's expert opinion on the current clinical use and future investigation for safer, more expansive use of these drugs. Results and Conclusions The panel recommends that physicians (1) conduct and document a formal risk assessment for existing cardiovascular disease and potential cardiovascular complications before VSP inhibitor treatment recognizing that preexisting hypertension and cardiovascular disease are common in patients with cancer, (2) actively monitor for blood pressure elevations and cardiac toxicity with more frequent assessments during the first treatment cycle, and (3) aggressively manage blood pressure elevations and early symptoms and signs of cardiac toxicity to prevent clinically limiting complications of VSP inhibitor therapy.</description><subject>Antineoplastic Agents - adverse effects</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Cancer therapies</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular</subject><subject>Cardiovascular Diseases - chemically induced</subject><subject>Cardiovascular Diseases - epidemiology</subject><subject>Cardiovascular Diseases - prevention & control</subject><subject>Cardiovascular System - drug effects</subject><subject>Cholesterol</subject><subject>Disease Management</subject><subject>Drug therapy</subject><subject>Epidermal Growth Factor - antagonists & inhibitors</subject><subject>Global Health</subject><subject>Heart attacks</subject><subject>Humans</subject><subject>Incidence</subject><subject>Kinases</subject><subject>Medical sciences</subject><subject>Neoplasms - drug therapy</subject><subject>Risk Factors</subject><subject>Signal Transduction - drug effects</subject><subject>Vascular endothelial growth factor</subject><issn>0002-8703</issn><issn>1097-6744</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kt-L1DAQx4Mo3rr6B_giARF96ZpfbRIEQQ5_wYkP6nNI03Sb2m33knTP_e-dsqsH93AvCZP5zGRmvoPQc0o2lNDqbb-xXb9hhFKwN4SqB2hFiZZFJYV4iFaEEFYoSfgFepJSD2bFVPUYXTDGSak4XaH8zY5263d-zHhqsbOxCdbhPP0JLuQjDiPe2xzAnXD0zodDGLf4YJObBxuxH5spd34IdsDbON3kDrfW5SniFLajHRYY4rsbu6TqQh3Al56iR60dkn92vtfo16ePPy-_FFffP3-9_HBVuLISuShlWwlRsUpQromQDZGsFd6Xqpa11koqWbKyaRURjWC8toKVTpdaae5IS0u-Rq9Pefdxup59ymYXkvPDYEc_zcloRpZBaA3km3tJqrjkTEnOAX15B-2nOUKvQEG5igsKxxrRE-XilFL0rdnHsLPxaCgxi3imNyCeWcRbnkA8iHlxzjzXO9_8j_inFgCvzgDM3w5ttKML6ZYrdcUrLYB7d-I8DPcQfDTJgYTONwE0zKaZwr1lvL8T7UDHAB_-9kefbrs1iRlifixbtiwZpYRIqRj_C68qyw8</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>Steingart, Richard M., MD</creator><creator>Bakris, George L., MD</creator><creator>Chen, Helen X., MD</creator><creator>Chen, Ming-Hui, MD, MMSc</creator><creator>Force, Thomas, MD</creator><creator>Ivy, S. 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Percy, MD ; Leier, Carl V., MD ; Liu, Glenn, MD ; Lenihan, Daniel, MD ; Lindenfeld, JoAnn, MD ; Maitland, Michael L., MD, PhD ; Remick, Scot C., MD ; Tang, W.H. Wilson, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c564t-57f6446264139047d072f4ee58b7b998787525df804d423ba425c959893c0f153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Antineoplastic Agents - adverse effects</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Cancer therapies</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular</topic><topic>Cardiovascular Diseases - chemically induced</topic><topic>Cardiovascular Diseases - epidemiology</topic><topic>Cardiovascular Diseases - prevention & control</topic><topic>Cardiovascular System - drug effects</topic><topic>Cholesterol</topic><topic>Disease Management</topic><topic>Drug therapy</topic><topic>Epidermal Growth Factor - antagonists & inhibitors</topic><topic>Global Health</topic><topic>Heart attacks</topic><topic>Humans</topic><topic>Incidence</topic><topic>Kinases</topic><topic>Medical sciences</topic><topic>Neoplasms - drug therapy</topic><topic>Risk Factors</topic><topic>Signal Transduction - drug effects</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Steingart, Richard M., MD</creatorcontrib><creatorcontrib>Bakris, George L., MD</creatorcontrib><creatorcontrib>Chen, Helen X., MD</creatorcontrib><creatorcontrib>Chen, Ming-Hui, MD, MMSc</creatorcontrib><creatorcontrib>Force, Thomas, MD</creatorcontrib><creatorcontrib>Ivy, S. 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Percy, MD</au><au>Leier, Carl V., MD</au><au>Liu, Glenn, MD</au><au>Lenihan, Daniel, MD</au><au>Lindenfeld, JoAnn, MD</au><au>Maitland, Michael L., MD, PhD</au><au>Remick, Scot C., MD</au><au>Tang, W.H. Wilson, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Management of cardiac toxicity in patients receiving vascular endothelial growth factor signaling pathway inhibitors</atitle><jtitle>The American heart journal</jtitle><addtitle>Am Heart J</addtitle><date>2012-02-01</date><risdate>2012</risdate><volume>163</volume><issue>2</issue><spage>156</spage><epage>163</epage><pages>156-163</pages><issn>0002-8703</issn><eissn>1097-6744</eissn><coden>AHJOA2</coden><abstract>Background Interfering with angiogenesis is an effective, widely used approach to cancer therapy, but antiangiogenic therapies have been associated with important systemic cardiovascular toxicities such as hypertension, left ventricular dysfunction, heart failure, and myocardial ischemia and infarction. As the use of vascular endothelial growth factor signaling pathway (VSP) inhibitors broadens to include older patients and those with existing cardiovascular disease, the adverse effects are likely to be more frequent, and cardiologists will increasingly be enlisted to help oncologists manage patients who develop adverse cardiovascular effects. Methods The Cardiovascular Toxicities Panel of the National Cancer Institute reviewed the published literature and abstracts from major meetings, shared experience gained during clinical development of VSP inhibitors, and contributed extensive clinical experience in evaluating and treating patients with cancer with cardiovascular disease. This report was edited and approved by the National Cancer Institute Investigational Drug Steering Committee. It presents the panel's expert opinion on the current clinical use and future investigation for safer, more expansive use of these drugs. Results and Conclusions The panel recommends that physicians (1) conduct and document a formal risk assessment for existing cardiovascular disease and potential cardiovascular complications before VSP inhibitor treatment recognizing that preexisting hypertension and cardiovascular disease are common in patients with cancer, (2) actively monitor for blood pressure elevations and cardiac toxicity with more frequent assessments during the first treatment cycle, and (3) aggressively manage blood pressure elevations and early symptoms and signs of cardiac toxicity to prevent clinically limiting complications of VSP inhibitor therapy.</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>22305831</pmid><doi>10.1016/j.ahj.2011.10.018</doi><tpages>8</tpages></addata></record> |
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subjects | Antineoplastic Agents - adverse effects Antineoplastic Agents - therapeutic use Biological and medical sciences Cancer therapies Cardiology. Vascular system Cardiovascular Cardiovascular Diseases - chemically induced Cardiovascular Diseases - epidemiology Cardiovascular Diseases - prevention & control Cardiovascular System - drug effects Cholesterol Disease Management Drug therapy Epidermal Growth Factor - antagonists & inhibitors Global Health Heart attacks Humans Incidence Kinases Medical sciences Neoplasms - drug therapy Risk Factors Signal Transduction - drug effects Vascular endothelial growth factor |
title | Management of cardiac toxicity in patients receiving vascular endothelial growth factor signaling pathway inhibitors |
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