Here, we discuss the etiologies, prevention, and management of cardiac toxicities in cancer survivors, considering cancer-related, treatment-related, and patient-related risks and effects. Programs in place to address cardiovascular risk factors in cancer survivors are highlighted.
Oncology (Williston Park). 30(12):1095–1098.
Table. Cardioprotective Lifestyle Modifications
Survival of cancer patients has improved dramatically in the past several decades; the 5-year overall survival rate in the United States was 49% in the 1970s but rose to 67% by 2012.[1,2] Advances in cancer survival have exposed risks of death from other causes, such as cardiovascular disease (CVD), the leading cause of death in the United States and the leading cause of death in survivors of early breast cancer.[3-5] Cancer treatments such as systemic therapy (not only with traditional chemotherapy but also with targeted agents and immunotherapy) and radiation therapy induce myriad cardiac toxicities that are frequently underappreciated. Here, we discuss the etiologies, prevention, and management of cardiac toxicities in cancer survivors, considering cancer-related, treatment-related, and patient-related risks and effects. Programs in place to address cardiovascular risk factors in cancer survivors are highlighted.
Cancer and CVD share common risk factors that induce inflammation and oxidative stress.[6] Inflammation, a hallmark of cancer, not only triggers mutagenesis and contributes to cancer pathophysiology,[7-9] but also is associated with cardiac disease and atherosclerosis.[10] Chronic systemic inflammation can lead to metabolic dysregulation, atherosclerosis,[11] cachexia and muscle wasting, and impaired regeneration of cardiac muscle.[12] These conditions increase the risk of coronary artery vasospasm, coronary artery disease (CAD), cardiomyopathies, and cardiac ischemia and infarction in cancer survivors.[13] Age-related cardiovascular risk is also a contributing factor: 86% of new cancers diagnosed in the United States occur in patients over age 50, a group already at increased risk for CVD in the general population.[1]
The cardiotoxicities of chemotherapy and radiation therapy can be broadly classified as acute or late effects. The acute effects of cancer treatment primarily impact the vascular system, specifically leading to hypertension, vasospasm, and thrombosis (including venous thromboembolic disease and rupture of arterial plaques). Late effects are long-term toxicities that generally involve structural cardiovascular changes, including atherosclerosis, valvular heart disease, and conduction system disease. Chemotherapy-induced cardiomyopathy often occurs during active treatment but may have a delayed onset.
Hypertension is a recognized long-term consequence of exposure to several chemotherapeutic agents.[14] It has also been observed acutely in the context of antiangiogenic therapies. Agents that inhibit vascular endothelial growth factor and its receptors-such as bevacizumab, sunitinib, sorafenib, and pazopanib-cause hypertension in up to 80% of patients.[15,16] The primary etiology of this effect is vasoconstriction through nitric oxide blockade and inhibition of other endothelium-derived vasodilatory factors.[17] The key to its management is patient education and on-treatment monitoring. No specific guidelines exist for initiation or selection of antihypertensive therapy in patients and survivors of cancer. However, it is generally appropriate to adhere to guidelines from the Eighth Joint National Committee,[18] which recommend diuretics, dihydropyridine calcium channel blockers, and angiotensin-converting enzyme inhibitors or angiotensin receptor blockers, taking into account individual patient comorbidities (such as diabetes mellitus, kidney disease). Nonselective beta-blockers such as labetalol and carvedilol are also effective antihypertensive agents that may be especially appropriate in patients with known coronary disease, given their proven efficacy in secondary prevention.[19]
Arterial or venous thrombosis can occur at increased frequency throughout chemotherapeutic treatment and beyond. Arterial thrombotic events most often occur as a consequence of plaque rupture at sites of atherosclerosis, which can exist from baseline disease or develop as a result of radiation therapy.[20] Since cancer is associated with hypercoagulability, cancer survivors are at higher risk of venous thromboembolism, which can be caused by the use of central venous catheters during chemotherapy.[14]
While no precise intervention can completely prevent the formation of blood clots, precautionary measures should be taken to reduce the risk. Cancer patients and survivors should avoid prolonged immobile states without ambulation, and indwelling venous access lines should be regularly maintained and replaced. Additionally, as in patients without cancer, regular exercise, proper nutrition, and avoidance of tobacco are critical lifestyle modifications to reduce the risk and progression of atherosclerosis. Patients with known coronary atherosclerosis should be maintained on low-dose aspirin for primary prevention in the absence of contraindications such as thrombocytopenia. Once a thrombotic event has occurred and been treated appropriately, long-term antithrombotic therapy with aspirin, warfarin, or direct oral anticoagulants should be considered for secondary prevention.[14]
Accelerated atherosclerosis is frequently seen in cancer survivors, particularly as a late effect of localized radiation therapy. The risk is dependent on the affected vasculature within the radiation field; mediastinal irradiation is associated with CAD,[21] neck irradiation with carotid disease,[22] abdominal irradiation with mesenteric ischemia, and limb irradiation with peripheral vascular disease.[23,24] In patients with concomitant cardiovascular risk factors in addition to a history of radiation therapy, targeted screening tests such as electrocardiograms (ECGs) and echocardiograms, stress testing for CAD, Doppler ultrasound for carotid and peripheral vascular disease, and annual evaluation of lipid profiles and thyroid-stimulating hormone levels may be indicated to provide further risk stratification.[14] If evidence of disease is found, the most effective intervention entails aggressive risk factor management. Pharmacologic therapies include antiplatelet therapy (including aspirin and P2Y12 receptor antagonists when appropriate), statin-based lipid-lowering agents, and antihypertensive therapy. Nonpharmacologic measures include regular aerobic exercise, improved nutrition, and cessation of tobacco and alcohol abuse.[25,26] Cardiovascular mortality is greater in patients whose CAD is associated with radiation therapy rather than CAD associated with atherosclerosis occurring after percutaneous interventions.[27] Accordingly, early detection and initiation of treatment are paramount.
Valvular disease, including both stenosis and regurgitation, occurs most notably after mediastinal radiation.[20] Radiation-induced inflammation leads to fibrotic thickening, valvular retraction, and accelerated calcification.[28] Mild to moderate valvular disease is usually clinically silent unless a patient has limited cardiopulmonary reserve. Therefore, patients should undergo serial assessments with clinical evaluation, ECG, and echocardiography, often in consultation with the cardiology team in order to optimize assessment intervals. If necessary, cardiothoracic surgery team input should be sought for consideration of valve repair or replacement.
Cardiac conduction system disease has also been observed after radiation therapy and chemotherapy. The involved fields in chest and mantle field irradiation invariably envelop some portion of the heart. Progressive radiation-induced cardiac injury may lead to bradyarrhythmias (sick sinus syndrome, atrioventricular block, QT prolongation) and tachyarrhythmias (atrial fibrillation, supraventricular tachycardia).[29,30] Atrial fibrillation can also be provoked by various chemotherapeutic agents, including ibrutinib, cisplatin, docetaxel, fluorouracil, gemcitabine, ifosfamide, and etoposide.[31,32] Symptoms suggestive of a conduction system abnormality, such as palpitations or syncope, should prompt monitoring using an ECG and a Holter monitor or event monitor, as well as a cardiology referral, if appropriate, for further patient evaluation and management. An echocardiogram should be performed for most patients with arrhythmias, and some patients may warrant coronary assessment for ischemia. Electrophysiology referral may be necessary for symptomatic bradyarrhythmias requiring a permanent pacemaker, refractory supraventricular arrhythmias requiring antiarrhythmic agents or ablation, or ventricular arrhythmias requiring an implantable cardioverter-defibrillator.[20]
A well-known long-term complication of anthracyclines and trastuzumab is cardiomyopathy leading to congestive heart failure. The pathophysiology and management of this complication have been discussed extensively throughout the literature.[33-36] Given the increased awareness about the acute and late cardiotoxic effects of cancer treatment modalities, it should be noted that significant changes in practice patterns are likely to shift the spectrum of cardiotoxicity in cancer survivors. The administration of anthracyclines is restricted to lifetime dose limits, and in combined regimens these agents are often replaced by alternatives.[37] In recent years, the use of advanced technologies (intensity-modulated radiation therapy, stereotactic body radiation therapy) has decreased the incidence of unintentional cardiac dosing. These changes are likely to lead to a decreased prevalence of cardiotoxicity among long-term cancer survivors in the coming decades.
Finally, newer treatment modalities such as immune checkpoint inhibition (against cytotoxic T-lymphocyte–associated antigen 4, programmed death 1, and programmed death ligand 1) can cause systemic inflammation and cardiac toxicity, including end-organ myofibrosis, autoimmune myocarditis, and acute heart failure.[38-40] However, in light of the relatively recent advances in development of various immunotherapies, their associated mechanisms of cardiotoxicity need to be explored further.
The most broadly effective intervention to address cardiovascular risk factors in cancer survivors is the adoption of healthy lifestyle behaviors as recommended by the American Cancer Society,[41,42] American Society of Clinical Oncology,[43] the National Comprehensive Cancer Network,[44] and the World Health Organization.[45] Each of these organizations recognizes the importance of a plant-based diet and regular physical activity in order to combat treatment-associated metabolic changes and reduce the risk of CAD. Physical activity has been shown to improve cardiovascular fitness in early breast cancer survivors, which results in enhanced daily function and quality of life,[46] and to reduce cardiovascular events among survivors of Hodgkin lymphoma.[47] Although the benefits of lifestyle modifications are intuitive, research is underway to investigate the effects of diet and exercise on cancer recurrence (ClinicalTrials.gov identifier: NCT02750826) and metabolic syndrome.[48] Currently, the National Institutes of Health has a program announcement to further study outcomes in cancer treatment–related cardiotoxicity,[49] including a research focus on behavioral interventions to mitigate or reverse cardiovascular damage.
As the overall survival of patients with cancer continues to rise, more cancer survivors are faced with the risk of developing treatment-related cardiovascular toxicities. Focused early patient evaluation and disease detection can stem the overall progression of cardiovascular-related debilitation, but prior cancer treatments are certainly not the sole culprits. Both cancer and CVD are characterized by a pro-inflammatory, mutagenic state, which can persist into the post-treatment period of survivorship and compound the risks of further cardiovascular decline. An effective approach to addressing cardiovascular toxicity in cancer survivors entails efforts to reduce risk factors through patient education and health promotion; diligent monitoring for early signs of toxicity; and coordinating patient management among the disciplines of oncology, cardiology, and primary care.
Financial Disclosure:The authors have no significant interest in or other relationship with the manufacturer of any product or provider of any service mentioned in this article.
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