Literature DB >> 22719160

Doxorubicin-induced cardiomyopathy 17 years after chemotherapy.

Simi Kumar1, Ravi Marfatia, Susan Tannenbaum, Clifford Yang, Erick Avelar.   

Abstract

Doxorubicin, an anthracycline antibiotic commonly used as a chemotherapeutic agent for breast cancer, is well known to cause cardiotoxicity. We report the case of an active, otherwise healthy 57-year-old breast cancer survivor who, 17 years after chemotherapy, presented with symptoms of overt heart failure. She had no cardiac risk factors, and neither laboratory nor imaging findings suggested myocarditis or dilated cardiomyopathy. Echocardiographic findings and differential diagnosis led us to attribute her condition to late doxorubicin-induced cardiomyopathy. By virtue of tapered medical therapy, her left ventricular ejection fraction improved from 0.20 to 0.55 in 8 months, and she was asymptomatic after 1 year. The reversibility of left ventricular dysfunction in our patient and the very late appearance of cardiotoxicity secondary to doxorubicin therapy raise questions about the pathogenesis and prevalence of late doxorubicin-induced cardiomyopathy and how to improve outcomes in patients who present with related symptoms of heart failure.

Entities:  

Keywords:  Adult; cardiomyopathies/chemically induced; cardiovascular diseases/therapy; doxorubicin/adverse effects; heart failure/chemically induced; risk factors; ventricular function, left/drug effects

Mesh:

Substances:

Year:  2012        PMID: 22719160      PMCID: PMC3368447     

Source DB:  PubMed          Journal:  Tex Heart Inst J        ISSN: 0730-2347


  14 in total

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Journal:  Ann Intern Med       Date:  1996-07-01       Impact factor: 25.391

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

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Journal:  Cancer       Date:  2003-06-01       Impact factor: 6.860

8.  Late doxorubicin cardiotoxicity.

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Journal:  Anticancer Drugs       Date:  1992-08       Impact factor: 2.248

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Review 10.  Cardiovascular complications of cancer therapy: incidence, pathogenesis, diagnosis, and management.

Authors:  Edward T H Yeh; Courtney L Bickford
Journal:  J Am Coll Cardiol       Date:  2009-06-16       Impact factor: 24.094

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4.  Mitochondrial topoisomerase I (top1mt) is a novel limiting factor of doxorubicin cardiotoxicity.

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Journal:  Tex Heart Inst J       Date:  2012

7.  Mesenchymal Stem Cell-Derived Small Extracellular Vesicles Protect Cardiomyocytes from Doxorubicin-Induced Cardiomyopathy by Upregulating Survivin Expression via the miR-199a-3p-Akt-Sp1/p53 Signaling Pathway.

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Review 8.  Human-induced pluripotent stem cell-derived cardiomyocytes, 3D cardiac structures, and heart-on-a-chip as tools for drug research.

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9.  Doxorubicin-Induced Cardiac Toxicity Is Mediated by Lowering of Peroxisome Proliferator-Activated Receptor δ Expression in Rats.

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