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Table of Contents
Vol. 115, No. 2, 2010
Issue release date: January 2010
Section title: Review
Free Access
Cardiology 2010;115:155–162
(DOI:10.1159/000265166)

Doxorubicin Cardiomyopathy

Chatterjee K.a · Zhang J.b · Honbo N.b · Karliner J.S.b, c
aDepartment of Medicine, University of Iowa Carver College of Medicine, Iowa City, Iowa, bCardiology Section (111C5), VA Medical Center, and cCardiovascular Research Institute, University of California, San Francisco, Calif., USA
email Corresponding Author

Abstract

Established doxorubicin cardiomyopathy is a lethal disease. When congestive heart failure develops, mortality is approximately 50%. Extensive research has been done to understand the mechanism and pathophysiology of doxorubicin cardiomyopathy, and considerable knowledge and experience has been gained. Unfortunately, no effective treatment for established doxorubicin cardiomyopathy is presently available. Extensive research has been done and is being done to discover preventive treatments. However an effective and clinically applicable preventive treatment is yet to be discovered.

© 2009 S. Karger AG, Basel


  

Key Words

  • Adriamycin
  • Anthracyclines
  • Cardiomyocytes
  • Cardiomyopathy
  • Doxorubicin
  • Vincristine

 Introduction

The anthracycline anticancer drug doxorubicin is an effective and frequently used chemotherapeutic agent for various malignancies [1,2]. Its major adverse effect is cardiotoxicity, which may limit its use. Doxorubicin cardiomyopathy, once developed, carries a poor prognosis and is frequently fatal [2,3]. The presently available treatment of established cardiomyopathy does not appear to improve prognosis. Thus, many preventive treatments have been proposed. This review briefly discusses the pathophysiology and management strategies of doxorubicin cardiomyopathy including the experimental drugs that have been tested to prevent its cardiotoxicity.

 

 Cardiotoxicity: Incidence

Doxorubicin cardiotoxicity can be acute, occurring during and within 2–3 days of its administration. The incidence of acute cardiotoxicity is approximately 11% [3,4]. The manifestations are usually chest pain due to myopericarditis and/or palpitations due to sinus tachycardia, paroxysmal nonsustained supraventricular tachycardia and premature atrial and ventricular beats. The electrocardiogram may reveal nonspecific ST-T changes, left axis deviation and decreased amplitude of QRS complexes. The mechanisms for these acute changes are not clear but may be due to doxorubicin-induced myocardial edema, which is reversible [3,5]. Acute left-ventricular (LV) failure is a rare manifestation of acute cardiotoxicity, but it is also reversible with appropriate treatments.

The incidence of chronic doxorubicin cardiotoxicity is much lower, with an estimated incidence of about 1.7% [6]. It is usually evident within 30 days of administration of its last dose, but it may occur even after 6–10 years after its administration. The incidence of doxorubicin cardiomyopathy is primarily related to its dose. The incidence is about 4% when the dose of doxorubicin is 500–550 mg/m2, 18% when the dose is 551–600 mg/m2 and 36% when the dose exceeds 600 mg/m2 [7]. The other risk factors are combination therapy with other cardiotoxic antitumor drugs and mediastinal radiation therapy. Cancer therapy in childhood and adolescence predisposes to the development of doxorubicin cardiomyopathy in adults [8]. Age also influences the risk of developing doxorubicin cardiomyopathy. Very young and very old individuals are more prone to develop this complication. A history of cardiovascular disease such as hypertension and reduced LV ejection fraction before therapy is also a risk factor to develop this complication. The prognosis of patients who develop congestive heart failure is poor (∼50% mortality in 1 year) [6].

 

 Cardiac Morphologic and Functional Changes

The cardiac morphologic and functional derangements of doxorubicin cardiomyopathy are similar to those of dilated cardiomyopathy. All four cardiac chambers may be dilated although severe dilatations of ventricles and atria are less common than in ischemic and non-ischemic dilated cardiomyopathies. The ventricular ejection fraction and contractile function is reduced. There is concomitant diastolic dysfunction. Because of insignificant change in LV wall thickness, wall stress is increased. Mural thrombi are also detected in some patients.

 

 Histopathologic Changes

In doxorubicin cardiomyopathy, there are areas of patchy myocardial interstitial fibrosis and scattered vacuolated cardiomyocytes (Adria cells; fig. 1). Adria cells are seen adjacent to areas of fibrosis. The areas of fibrosis are usually widespread and areas of acute myocyte damage are infrequent. There is fibroblast proliferation and histiocyte infiltration in the areas of healed myocarditis. Partial or total loss of myofibrils and myocyte vacuolar degeneration are essential features of doxorubicin cardiotoxicity (fig. 2). With loss of myofilaments, the remnants of Z discs are seen. There is distention of sarcoplasmic reticulum and the T-tubules. The myocyte vacuoles coalesce and form large membrane-bound spaces. The nucleus-chromatin disorganization and replacement of chromatin by pale filaments are also features of doxorubicin cardiomyopathy [3,9,10].

FIG01
Fig. 1.a Normal myocyte structure and without abnormal interstitial fibrosis. b Myofibrillar loss and vacuolization (Adria cells) and extensive diffuse fibrosis. (Published with permission from Takemura et al. [3])

FIG02
Fig. 2.a Normal myocardium with little or no extracellular matrix changes and intact myocytes. b Same features in higher magnification. c Myocyte loss, matrix disorganization and diffuse fibrosis. (Published with permission from Takemura et al. [3])

 

 Mechanism of Doxorubicin Cardiomyopathy

The mechanisms of therapeutic effects of doxorubicin on tumor cells are different from those of the mechanisms of its cardiotoxicity. The proposed mechanisms of its anti-malignancy effects include intercalation into DNA leading to inhibition of synthesis of macromolecules, generation of reactive oxygen species, DNA binding and DNA cross-linking; DNA damage by inhibition of topoisomerase II, and induction of apoptosis by inhibition of topoisomerase II [3,11,12].

The proposed principal mechanisms of doxorubicin cardiotoxicity are increased oxidative stress, as evident from increased levels of reactive oxygen species and lipid peroxidation [3,5,13,14]. Decreased levels of antioxidants and sulfhydryl groups [5,15,16,17,18], inhibition of nucleic acid and protein synthesis [19,20], release of vasoactive amines [21], altered adrenergic function [22] and decreased expression of cardiac-specific genes are other proposed mechanisms [3]. It is possible that more than one mechanism is operative. It should also be emphasized that the importance of many of the proposed mechanisms remains to be established.

 Oxidative Stress

Doxorubicin appears to induce toxic damage to the mitochondria of cardiomyocytes. Several mitochondrial enzymes such as NADH dehydrogenase, cytochrome P-450 reductase and xanthine oxidase are involved in generating oxygen free radicals (reactive oxygen species) [3,23,24,25]. Doxorubicin also increases superoxide formation by increasing endothelial nitric oxide synthase [26,27], which promotes intracellular hydrogen peroxide formation [28].

 Gene Expression

The downregulation of α-actin, myosin light and heavy chains, troponin-I, and desmin proteins by doxorubicin has been suggested as a potential mechanism of its cardiotoxicity. Decreased expression of the contractile proteins is associated with myofibrillar loss and reduced myocardial contractile function [29,30]. Downregulation of sarcoplasmic reticular ATPase may cause abnormal myocardial diastolic function [3,29,30]. It has been suggested that doxorubicin can inactivate extracellular signal-regulated kinase (ERK) [31].

 Apoptosis

There is evidence that doxorubicin induces apoptosis of cardiomyocytes [28,32,33]. Formation of hydrogen peroxide and superoxide has been implicated in doxorubicin-induced cardiomyocyte toxicity [28,32]. These intracellular oxidants induce p53, and activated p53 promotes apoptosis of cardiomyocytes [35,36].

 

 Diagnosis

The diagnosis of doxorubicin cardiomyopathy should consist of taking appropriate history to assess the likelihood of the diagnosis. A complete examination of the cardiovascular system to detect presence of signs of overt heart failure, such as elevated jugular venous pressure and S3 gallop, is essential. An electrocardiogram should be obtained, which usually demonstrates nonspecific ST-T wave changes and sometimes low-voltage QRS complexes. A chest X-ray is also helpful to assess cardiomegaly and signs of pulmonary venous congestion. It should be emphasized that the presence or absence of the abnormalities by these evaluations are nonspecific and nondiagnostic.

Echocardiography with Doppler studies is commonly used to detect early diastolic and systolic LV dysfunction. Exercise echocardiography may also be useful to assess LV contractile reserve.

Radionuclide ventriculography has been used to assess LV systolic and diastolic function. Like other types of cardiomyopathy, cardiac adrenergic denervation occurs in doxorubicin cardiomyopathy. MIBG (metaiodobenzylguanidine) nuclear imaging can be employed to assess cardiac adrenergic denervation [37]. Impaired glucose and fatty acid metabolism has been observed in doxorubicin cardiomyopathy. Impaired myocardial glucose uptake can be assessed by positron emission tomography using fluorine-18F-deoxyglucose [3]. Abnormal fatty acid metabolism can be assessed by 123I-BMIPP (β-methyl-branched fatty acid) nuclear studies [38]. Cardiac magnetic resonance imaging can also be used to assess LV systolic function. These tests however are not specific for doxorubicin cardiomyopathy.

Antimyosin antibody study with the use of 111In-labeled monoclonal antimyosin antibody is used for the diagnosis of myocarditis and has also been employed for the diagnosis of doxorubicin cardiomyopathy [39]. In doxorubicin-treated patients, the sensitivity of antimyosin antibody studies is very high [40]. Various nuclear studies to detect apoptosis have been tested in animal models [41]. Annexin V, which has high affinity for membrane-bound phosphatidylserine, has been used to detect apoptosis induced by doxorubicin.

The measurements of neurohormones and cardiac enzymes have been used for the diagnosis of doxorubicin cardiotoxicity and presence of heart failure. Plasma levels of B-type natriuretic peptide are elevated and correlate with the severity of congestive heart failure [42]. The troponin T or I levels may also be increased, indicating myocardial injury [43]. The changes in neurohormones and cardiac enzymes are not diagnostic of doxorubicin cardiomyopathy and are observed in other types of cardiomyopathy. The endomyocardial biopsy may reveal characteristic diagnostic features of doxorubicin cardiomyopathy. The findings that have been suggested for the diagnosis of doxorubicin cardiomyopathy are loss of myofibrils, distention of sarcoplasmic reticulum, and vacuolization of the cytoplasm. The endomyocardial biopsy is also used to grade the severity of doxorubicin cardiotoxicity [3,9,21]. The disadvantage of this technique is that it is invasive, and it requires considerable experience and training. Furthermore, endomyocardial biopsies are not universally used for the diagnosis of doxorubicin cardiomyopathy and its severity.

 

 Management

There is no specific treatment available for the management of patients with established heart failure. Diuretics are used to relieve symptoms and signs of pulmonary and systemic venous congestion. β-Adrenergic blocking agents should be considered, as for treatment of other types of systolic heart failure [44]. It has been reported that metoprolol is safe and can be effective in doxorubicin-induced cardiomyopathy [45]. However, there are no controlled studies performed to determine whether β-blocker treatments are effective to prevent progression of remodeling and to improve prognosis [44]. There is also no information available, to the best of our knowledge, whether there has been any change in prognosis of doxorubicin cardiomyopathy before and after introduction of β-blocker therapy. Angiotensin II inhibition should also be considered [3]. In patients with advanced heart failure and in those intolerant to angiotensin II inhibition therapy, low-dose hydralazine-isosorbide dinitrate combination treatment is often employed; however there is no information available to suggest that such treatment is effective in patients with doxorubicin cardiomyopathy. In patients with malignant arrhythmias, amiodarone and implantable cardioverter and defibrillator should be considered. It should be appreciated that none of the treatments employed for ischemic or idiopathic dilated cardiomyopathy has been demonstrated to improve the prognosis of patients with doxorubicin cardiomyopathy. Cardiac transplantation has been reported to improve long-term prognosis of the patients in whom the primary malignancy is cured following chemotherapy [46,47]. Placement of ventricular assist devices may be required before cardiac transplantation.

 

 Preventive Strategies

To date, the major emphasis has been to limit the cumulative dose of doxorubicin to <450 mg/m2 [4]. The use of anthracycline analogues, alternative methods of drug delivery and continuous slow infusion instead of standard infusion protocols have also been employed to reduce the risk of dilated cardiomyopathy. However, strategies to prevent or reduce doxorubicin cardiotoxicity have not been established [3].

A number of pharmaceutical agents have been tested, usually in experimental animal studies, to assess their potential to reduce the risk of doxorubicin cardiotoxicity (table 1). Most of the pharmacologic agents that have been tested to reduce or prevent doxorubicin cardiotoxicity have the potential to reduce oxidative stress [48]. The mercaptopropionyl glycine (MPG), a synthetic aminothiol that exhibits antioxidant properties, has been shown to reduce doxorubicin cardiotoxicity [49]. Similarly, probucol, super oxide dismutase, and dexrarzoxane with documented antioxidant properties have been reported to decrease doxorubicin cardiotoxicity [49,50,51]. Because the calcium channel blocker amlodipine and the β-and α-adrenergic blocking agent carvedilol have antioxidant properties they have also been studied for their potential to reduce doxorubicin cardiotoxicity [52,53]. The PDE5 inhibitor sildenafil, erythropoietin and thrombopoietin, granulocyte colony-stimulating factor, and the endothelin receptor-blocking agent bosentan have been used in experimental animal models for the protection against developing doxorubicin cardiomyopathy [54,55]. The potential protective role of nitric oxide and superoxide dismutase has been investigated in a transgenic mouse model. Lack of nitric oxide was associated with enhanced cardiac injury, and mitochondrial injury was attenuated by an increase in manganese superoxide dismutase [56].

TAB01
Table 1. A few pharmacologic agents that have been used to reduce doxorubicin cardiotoxicity

In our laboratory, we found that the vinca alkaloid vincristine exerts cardioprotective effects on cultured adult mouse cardiac myocytes to chemical and hypoxic oxidative stress [57]. Vincristine is often used in combination with doxorubicin to enhance the effectiveness for treatment of the malignancy. As vincristine reduced oxidative stress in the cultured adult myocytes, we evaluated the potential cardioprotective effect of vincristine against doxorubicin cardiotoxicity in the mouse adult cell culture model [58].

Myocyte survival was quantified by the trypan blue exclusion technique, which has been validated by previous studies [59,60]. A second technique to assess cell survival (live/dead viability/cytotoxicity assay) was also employed [58]. In figure 3, the effects of doxorubicin – either alone or in combination with vincristine – on myocyte survival during trypan blue and live/dead assays in a typical experiment are illustrated. It is clear that co-treatment with vincristine reduces the magnitude of doxorubicin-induced myocyte death [58]. The magnitude of protection by vincristine of doxorubicin-induced myocyte death is illustrated in figure 4. Exposure of cultured myocytes to 15 or 20 µg/ml of doxorubicin for approximately 24 h typically reduces myocyte survival by 50%. Co-treatment with 10–30 µmol/l of vincristine dramatically increased cardiomyocyte survival (>85%) [58].

FIG03
Fig. 3.a Results of trypan blue exclusion assay in a typical experiment demonstrating that co-treatment with vincristine (VCR) markedly decreases doxorubicin (DOX)-induced cardiomyocyte death. b Results of a live/dead assay. With doxorubicin treatment alone for 24 h there was an increased proportion of dead cells (ethidium positive, EthD/red fluorescence) and a decreased proportion of live cells (calcein ester positive/green fluorescence) compared to vehicle treatment. With co-treatment with vincristine there were more live than dead cells. (Published with permission from Chatterjee et al. [58])

FIG04
Fig. 4. The effects of increasing concentrations of vincristine (VCR) on the survival of cultured adult mouse myocytes exposed to doxorubicin (DOX; trypan blue assay). With doxorubicin treatment alone, myocyte survival was on average 50%. With vincristine co-treatment, survival was >85%. n = 5; * p < 0.05. (Published with permission from Chatterjee et al. [58])

The potential protective mechanisms of vincristine in reducing doxorubicin cardiomyocyte toxicity were explored in this experimental cultured adult mouse model. Phosphorylation of the survival signals PI3-K/AKT and MEK/ERK were observed. Doxorubicin inhibits these pathways. Concomitant use of the PI3-K/AKT and MEK/ERK inhibitors (LY294002 and PD98059, respectively) further reduced myocyte survival. During vincristine co-treatment without the inhibitors, myocyte salvage was >85%, as observed previously. With addition of the inhibitors, the magnitude of salvage by vincristine was substantially attenuated (fig. 5) [58]. These findings suggest that the protection by vincristine involves these survival pathways.

FIG05
Fig. 5. The effects of pharmacologic inhibitors of PI3-K/AKT (LY294002, LY) and MEK/ERK (PD 98059, PD) on cell survival (trypan blue assay) with or without doxorubicin (DOX) and vincristine (VCR) co-treatment. Doxorubicin treatment alone was associated with decreased myocyte survival. The addition of the inhibitors further decreased survival of the cardiomyocytes. With vincristine co-treatment without the inhibitors, survival was >85%. With the addition of the inhibitors, protection by vincristine was significantly attenuated, suggesting that survival pathways are involved in the protective effect of vincristine. n = 5–6; * p < 0.05. Con. = Control; Veh. = vehicle. (Published with permission from Chatterjee et al. [58])

Compared to doxorubicin treatment alone, co-treatment with vincristine decreased cytochrome c release, suggesting that vincristine decreases oxidative stress and inhibits mitochondrial transition. In this experimental model with cultured adult mouse myocytes, doxorubicin-induced apoptosis was assessed by TUNEL staining. Doxorubicin induces myocyte apoptosis within a few hours, which is markedly delayed with co-treatment with vincristine.

In this study, we compared the effects of vincristine to those of mercaptopropionyl glycine (which has antioxidant properties), amlodipine (a dyhydropyridine calcium channel blocker), and dexrazoxane (an iron-chelating agent). The survival of cardiomyocytes was determined by trypan blue assay. Vincristine was superior to mercaptopropionyl glycine and amlodipine but equal to dexrazoxane in salvaging cardiomyocytes exposed to doxorubicin [58].

It should be emphasized that most of the pharmacologic agents which have the potential to reduce doxorubicin cardiotoxicity have been studied in animals, usually during acute and short-term exposure to doxorubicin. In most studies, either mice or rats have been used and short-term intraperitoneal administration of doxorubicin has been employed. Various methods to assess cardiotoxicity have been used in different studies. The effects of vincristine may differ according to the species. In our studies, we used male C57B 1/6 adult mouse strains and it remains unknown whether vincristine will exert similar protective effects or not in other mouse and animal species and humans. Also, without appropriate clinical study, whether any of these agents will be useful in the treatment of doxorubicin cardiomyopathy will remain uncertain. Although the iron-chelating agent dexrazoxane is available for clinical use, in practice it is used infrequently because it can induce myelosuppression.

In conclusion, doxorubicin cardiomyopathy remains a lethal disease. Extensive investigations and research have been done to understand the mechanism of doxorubicin cardiotoxicity and substantial knowledge has been accumulated. Although extensive research has also been done to find effective treatment of doxorubicin cardiomyopathy, no such treatment has been discovered. Similarly, extensive research has been done and is being done to prevent doxorubicin cardiotoxicity. However, an effective preventive treatment is yet to be discovered.

 

 Acknowledgments

We are very grateful to Lauren Poull and Arlinda LaRose for their extraordinary help in the preparation of the manuscript.


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Author Contacts

Kanu Chatterjee
Division of Cardiology, Department of Medicine
University of Iowa Carver College of Medicine, Room/Bldg E-314-4 GH
200 Hawkins Drive, Iowa City, IA 52242-1081 (USA)
Tel. +1 319 353 7789, Fax +1 319 353 6343, E-Mail kanu-chatterjee@uiowa.edu

  

Article Information

Parts of this study were presented at the Annual Meetings of the European Society of Cardiology in 2007 and 2008.

Received: June 14, 2009
Accepted after revision: September 24, 2009
Published online: December 11, 2009
Number of Print Pages : 8
Number of Figures : 5, Number of Tables : 1, Number of References : 60

  

Publication Details

Cardiology (International Journal of Cardiovascular Medicine, Surgery, Pathology and Pharmacology)

Vol. 115, No. 2, Year 2010 (Cover Date: January 2010)

Journal Editor: Borer J.S. (New York, N.Y.)
ISSN: 0008-6312 (Print), eISSN: 1421-9751 (Online)

For additional information: http://www.karger.com/CRD


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