Literature DB >> 21050974

Left ventricular dysfunction in patients receiving cardiotoxic cancer therapies are clinicians responding optimally?

Geoffrey J Yoon1, Melinda L Telli, David P Kao, Kelly Y Matsuda, Robert W Carlson, Ronald M Witteles.   

Abstract

OBJECTIVES: The purpose of this study was to examine treatment practices for cancer therapy-associated decreased left ventricular ejection fraction (LVEF) detected on echocardiography and whether management was consistent with American College of Cardiology/American Heart Association guidelines.
BACKGROUND: Patients treated with anthracyclines or trastuzumab are at risk of cardiotoxicity. Decreased LVEF represents a Class I indication for drug intervention according to American College of Cardiology/American Heart Association guidelines.
METHODS: Patients receiving anthracycline or trastuzumab at Stanford University from October 2005 to October 2007 and who had undergone echocardiography before and after receiving an anthracycline or trastuzumab were identified. Chart review examined chemotherapy regimens, cardiac risk factors, imaging results, concomitant medications, and cardiology consultations.
RESULTS: Eighty-eight patients received therapy with an anthracycline or trastuzumab and had a pre-treatment and follow-up echocardiogram. Ninety-two percent were treated with anthracyclines, 17% with trastuzumab after an anthracycline, and 8% with trastuzumab without previous treatment with anthracycline. Mean baseline LVEF was 60%, with 14% having a baseline <55%. Forty percent had decreased LVEF (<55%) after anthracycline and/or trastuzumab treatment. Of these patients, 40% received angiotensin-converting enzyme inhibitor or angiotensin receptor blocker therapy, 51% beta-blocker therapy, and 54% cardiology consultation. Of patients with asymptomatic decreased LVEF, 31% received angiotensin-converting enzyme inhibitor or angiotensin receptor blocker therapy, 35% beta-blocker therapy, and 42% cardiology consultation. Of those with symptomatic decreased LVEF, 67% received angiotensin-converting enzyme inhibitor or angiotensin receptor blocker therapy, 100% beta-blocker therapy, and 89% cardiology consultation.
CONCLUSIONS: Many cancer survivors are not receiving treatment consistent with heart failure guidelines. There is substantial opportunity for collaboration between oncologists and cardiologists to improve the care of oncology patients receiving cardiotoxic therapy.
Copyright © 2010 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 21050974      PMCID: PMC3835691          DOI: 10.1016/j.jacc.2010.07.023

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  22 in total

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2.  Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2.

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Journal:  Cancer       Date:  1973-08       Impact factor: 6.860

4.  Is specialty care associated with improved survival of patients with congestive heart failure?

Authors:  Olafur S Indridason; Cynthia J Coffman; Eugene Z Oddone
Journal:  Am Heart J       Date:  2003-02       Impact factor: 4.749

5.  Risk factors for doxorubicin-induced congestive heart failure.

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Journal:  Ann Intern Med       Date:  1979-11       Impact factor: 25.391

6.  Natural history of asymptomatic left ventricular systolic dysfunction in the community.

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7.  Subclinical late cardiomyopathy after doxorubicin therapy for lymphoma in adults.

Authors:  O Hequet; Q H Le; I Moullet; E Pauli; G Salles; D Espinouse; C Dumontet; C Thieblemont; P Arnaud; D Antal; F Bouafia; B Coiffier
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8.  Functional monitoring of anthracycline cardiotoxicity: a prospective, blinded, long-term observational study of outcome in 120 patients.

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Journal:  Ann Oncol       Date:  2002-05       Impact factor: 32.976

9.  Congestive heart failure in patients treated with doxorubicin: a retrospective analysis of three trials.

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10.  Early decline in left ventricular ejection fraction predicts doxorubicin cardiotoxicity in lymphoma patients.

Authors:  T Nousiainen; E Jantunen; E Vanninen; J Hartikainen
Journal:  Br J Cancer       Date:  2002-06-05       Impact factor: 7.640

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  45 in total

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Review 7.  Doxorubicin-Induced Cardiomyopathy in Children.

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8.  The Role of Cardiovascular Magnetic Resonance Imaging in Heart Failure.

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Review 9.  Pharmacogenomics as a risk mitigation strategy for chemotherapeutic cardiotoxicity.

Authors:  Brian C Jensen; Howard L McLeod
Journal:  Pharmacogenomics       Date:  2013-01       Impact factor: 2.533

10.  Managing cardiotoxicity of chemotherapy.

Authors:  Alessandro Colombo; Carlo A Meroni; Carlo M Cipolla; Daniela Cardinale
Journal:  Curr Treat Options Cardiovasc Med       Date:  2013-08
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