Cardiovascular comorbidity in multiple sclerosis patients treated with Mitoxantrone therapy: a cohort study

Background Mitoxantrone (MX) has been used as second line therapy for aggressive multiple sclerosis (MS). Potential cardiotoxic effects of MX limit its use; a cumulative dose of up to 100 mg/m2, has been long considered relatively safe. We calculated the frequency of cardiac side effects in MS patie...

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Veröffentlicht in:Multiple sclerosis and demyelinating disorders 2017-07, Vol.2 (1), p.1, Article 12
Hauptverfasser: Ragonese, Paolo, Aridon, Paolo, Realmuto, Sabrina, Vazzoler, Giulia, Alessi, Simona, Portera, Erika, Bianchi, Alessia, Triolo, Fabio, Mazzola, Maria Antonietta, D’Amelio, Marco, Savettieri, Giovanni, Salemi, Giuseppe
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container_issue 1
container_start_page 1
container_title Multiple sclerosis and demyelinating disorders
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creator Ragonese, Paolo
Aridon, Paolo
Realmuto, Sabrina
Vazzoler, Giulia
Alessi, Simona
Portera, Erika
Bianchi, Alessia
Triolo, Fabio
Mazzola, Maria Antonietta
D’Amelio, Marco
Savettieri, Giovanni
Salemi, Giuseppe
description Background Mitoxantrone (MX) has been used as second line therapy for aggressive multiple sclerosis (MS). Potential cardiotoxic effects of MX limit its use; a cumulative dose of up to 100 mg/m2, has been long considered relatively safe. We calculated the frequency of cardiac side effects in MS patients treated with MX. Methods We performed a cohort study including all MS patients treated with MX at the Neurological Department of the University Hospital of Palermo, Italy. Two hundred-sixty-four MS patients diagnosed according to validated criteria were included and followed-up until the end of September 2010. Patients were treated with MX as a second line therapy if they had no previous heart diseases determined by clinical evaluation, electrocardiography, and echocardiography. Treatment administration was made at a monthly dose of 8 mg/m2 for the first three months and at a dose of 12 mg/m2 every three months. Echocardiography was routinely performed every six months. Treatment was stopped before reaching the final dose if signs had appeared of impaired heart function, confirmed left ventricular ejection fraction reduction lower to 50%, or a confirmed reduction of more than 10% with respect to the first examination. Results Heart involvement was observed in 12.4% of treated individuals, and symptomatic congestive heart failure occurred in 2.7% of the cohort. A patient had a myocardial infarction, and 3.1% showed electrocardiographic anomalies not present at baseline. Conclusion Our study confirms that cardiac adverse events associated with MX are more common than previously reported.
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Potential cardiotoxic effects of MX limit its use; a cumulative dose of up to 100 mg/m2, has been long considered relatively safe. We calculated the frequency of cardiac side effects in MS patients treated with MX. Methods We performed a cohort study including all MS patients treated with MX at the Neurological Department of the University Hospital of Palermo, Italy. Two hundred-sixty-four MS patients diagnosed according to validated criteria were included and followed-up until the end of September 2010. Patients were treated with MX as a second line therapy if they had no previous heart diseases determined by clinical evaluation, electrocardiography, and echocardiography. Treatment administration was made at a monthly dose of 8 mg/m2 for the first three months and at a dose of 12 mg/m2 every three months. Echocardiography was routinely performed every six months. Treatment was stopped before reaching the final dose if signs had appeared of impaired heart function, confirmed left ventricular ejection fraction reduction lower to 50%, or a confirmed reduction of more than 10% with respect to the first examination. Results Heart involvement was observed in 12.4% of treated individuals, and symptomatic congestive heart failure occurred in 2.7% of the cohort. A patient had a myocardial infarction, and 3.1% showed electrocardiographic anomalies not present at baseline. Conclusion Our study confirms that cardiac adverse events associated with MX are more common than previously reported.</description><identifier>ISSN: 2056-6115</identifier><identifier>EISSN: 2056-6115</identifier><identifier>DOI: 10.1186/s40893-017-0028-0</identifier><language>eng</language><publisher>London: BioMed Central</publisher><subject>Age ; Cardiac arrhythmia ; Cardiovascular disease ; Cohort analysis ; Drug dosages ; Heart attacks ; Heart failure ; Leukemia ; Multiple sclerosis ; Nervous system ; Patients ; Pneumonia ; Womens health</subject><ispartof>Multiple sclerosis and demyelinating disorders, 2017-07, Vol.2 (1), p.1, Article 12</ispartof><rights>2017. This work is licensed 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-c1610-c8d644b0b03e74d305d10404fd36807a1eee7692e89b37cf2fc7fe61f2cd31d83</citedby><cites>FETCH-LOGICAL-c1610-c8d644b0b03e74d305d10404fd36807a1eee7692e89b37cf2fc7fe61f2cd31d83</cites><orcidid>0000-0003-2516-1567</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27931,27932</link.rule.ids></links><search><creatorcontrib>Ragonese, Paolo</creatorcontrib><creatorcontrib>Aridon, Paolo</creatorcontrib><creatorcontrib>Realmuto, Sabrina</creatorcontrib><creatorcontrib>Vazzoler, Giulia</creatorcontrib><creatorcontrib>Alessi, Simona</creatorcontrib><creatorcontrib>Portera, Erika</creatorcontrib><creatorcontrib>Bianchi, Alessia</creatorcontrib><creatorcontrib>Triolo, Fabio</creatorcontrib><creatorcontrib>Mazzola, Maria Antonietta</creatorcontrib><creatorcontrib>D’Amelio, Marco</creatorcontrib><creatorcontrib>Savettieri, Giovanni</creatorcontrib><creatorcontrib>Salemi, Giuseppe</creatorcontrib><title>Cardiovascular comorbidity in multiple sclerosis patients treated with Mitoxantrone therapy: a cohort study</title><title>Multiple sclerosis and demyelinating disorders</title><description>Background Mitoxantrone (MX) has been used as second line therapy for aggressive multiple sclerosis (MS). Potential cardiotoxic effects of MX limit its use; a cumulative dose of up to 100 mg/m2, has been long considered relatively safe. We calculated the frequency of cardiac side effects in MS patients treated with MX. Methods We performed a cohort study including all MS patients treated with MX at the Neurological Department of the University Hospital of Palermo, Italy. Two hundred-sixty-four MS patients diagnosed according to validated criteria were included and followed-up until the end of September 2010. Patients were treated with MX as a second line therapy if they had no previous heart diseases determined by clinical evaluation, electrocardiography, and echocardiography. Treatment administration was made at a monthly dose of 8 mg/m2 for the first three months and at a dose of 12 mg/m2 every three months. Echocardiography was routinely performed every six months. Treatment was stopped before reaching the final dose if signs had appeared of impaired heart function, confirmed left ventricular ejection fraction reduction lower to 50%, or a confirmed reduction of more than 10% with respect to the first examination. Results Heart involvement was observed in 12.4% of treated individuals, and symptomatic congestive heart failure occurred in 2.7% of the cohort. A patient had a myocardial infarction, and 3.1% showed electrocardiographic anomalies not present at baseline. 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Aridon, Paolo ; Realmuto, Sabrina ; Vazzoler, Giulia ; Alessi, Simona ; Portera, Erika ; Bianchi, Alessia ; Triolo, Fabio ; Mazzola, Maria Antonietta ; D’Amelio, Marco ; Savettieri, Giovanni ; Salemi, Giuseppe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1610-c8d644b0b03e74d305d10404fd36807a1eee7692e89b37cf2fc7fe61f2cd31d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Age</topic><topic>Cardiac arrhythmia</topic><topic>Cardiovascular disease</topic><topic>Cohort analysis</topic><topic>Drug dosages</topic><topic>Heart attacks</topic><topic>Heart failure</topic><topic>Leukemia</topic><topic>Multiple sclerosis</topic><topic>Nervous system</topic><topic>Patients</topic><topic>Pneumonia</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ragonese, Paolo</creatorcontrib><creatorcontrib>Aridon, Paolo</creatorcontrib><creatorcontrib>Realmuto, Sabrina</creatorcontrib><creatorcontrib>Vazzoler, Giulia</creatorcontrib><creatorcontrib>Alessi, Simona</creatorcontrib><creatorcontrib>Portera, Erika</creatorcontrib><creatorcontrib>Bianchi, Alessia</creatorcontrib><creatorcontrib>Triolo, Fabio</creatorcontrib><creatorcontrib>Mazzola, Maria Antonietta</creatorcontrib><creatorcontrib>D’Amelio, Marco</creatorcontrib><creatorcontrib>Savettieri, Giovanni</creatorcontrib><creatorcontrib>Salemi, Giuseppe</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; 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Potential cardiotoxic effects of MX limit its use; a cumulative dose of up to 100 mg/m2, has been long considered relatively safe. We calculated the frequency of cardiac side effects in MS patients treated with MX. Methods We performed a cohort study including all MS patients treated with MX at the Neurological Department of the University Hospital of Palermo, Italy. Two hundred-sixty-four MS patients diagnosed according to validated criteria were included and followed-up until the end of September 2010. Patients were treated with MX as a second line therapy if they had no previous heart diseases determined by clinical evaluation, electrocardiography, and echocardiography. Treatment administration was made at a monthly dose of 8 mg/m2 for the first three months and at a dose of 12 mg/m2 every three months. Echocardiography was routinely performed every six months. Treatment was stopped before reaching the final dose if signs had appeared of impaired heart function, confirmed left ventricular ejection fraction reduction lower to 50%, or a confirmed reduction of more than 10% with respect to the first examination. Results Heart involvement was observed in 12.4% of treated individuals, and symptomatic congestive heart failure occurred in 2.7% of the cohort. A patient had a myocardial infarction, and 3.1% showed electrocardiographic anomalies not present at baseline. Conclusion Our study confirms that cardiac adverse events associated with MX are more common than previously reported.</abstract><cop>London</cop><pub>BioMed Central</pub><doi>10.1186/s40893-017-0028-0</doi><orcidid>https://orcid.org/0000-0003-2516-1567</orcidid><oa>free_for_read</oa></addata></record>
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subjects Age
Cardiac arrhythmia
Cardiovascular disease
Cohort analysis
Drug dosages
Heart attacks
Heart failure
Leukemia
Multiple sclerosis
Nervous system
Patients
Pneumonia
Womens health
title Cardiovascular comorbidity in multiple sclerosis patients treated with Mitoxantrone therapy: a cohort study
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