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      Management of cardiovascular risk in patients with multiple myeloma

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          Abstract

          Multiple myeloma (MM) is a plasma cell malignancy that accounts for 10% of hematological cancers. It predominantly affects elderly people; median age at diagnosis is 70 years. Consequently, many patients with MM have cardiovascular comorbidities or risk factors. MM can cause cardiac comorbidities such as cardiomyopathy and heart failure caused by cardiac amyloidosis and/or anemia. Some of the treatments used in MM can also affect cardiovascular health. Advances in pharmacotherapy for MM, such as the introduction of immunomodulators, proteasome inhibitors, histone deacetylase inhibitors, and monoclonal antibodies, have dramatically improved progression-free survival and life expectancy, but new agent classes are associated with adverse events that were not previously observed on a regular basis, including cardiovascular events. However, with careful risk assessment, monitoring, and prophylactic therapy, many of these cardiovascular complications can be managed or treated successfully. Most routine cardiovascular surveillance is undertaken by the treating hemato-oncologist, but a multidisciplinary approach involving cardiologists may help to optimize patient outcomes. In this review, we survey the cardiac complications commonly reported in patients with MM, discuss how they can be prevented and managed, and summarize the role cardiologists can play in delivering the best possible outcomes for patients with MM and cardiovascular comorbidities.

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          Most cited references46

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          Multiple myeloma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up†

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            Cardiovascular toxicity induced by chemotherapy, targeted agents and radiotherapy: ESMO Clinical Practice Guidelines.

            Cardiovascular (CV) toxicity is a potential short- or long-term complication of various anticancer therapies. Some drugs, such as anthracyclines or other biological agents, have been implicated in causing potentially irreversible clinically important cardiac dysfunction. Although targeted therapies are considered less toxic and better tolerated by patients compared with classic chemotherapy agents, rare but serious complications have been described, and longer follow-up is needed to determine the exact profile and outcomes of related cardiac side-effects. Some of these side-effects are irreversible, leading to progressive CV disease, and some others induce reversible dysfunction with no long-term cardiac damage to the patient. Assessment of the prevalence, type and severity of cardiac toxicity caused by various cancer treatments is a breakthrough topic for patient management. Guidelines for preventing, monitoring and treating cardiac side-effects are a major medical need. Efforts are needed to promote strategies for cardiac risk prevention, detection and management, avoiding unintended consequences that can impede development, regulatory approval and patient access to novel therapy. These new ESMO Clinical Practice Guidelines are the result of a multidisciplinary cardio-oncology review of current evidence with the ultimate goal of providing strict criteria-based recommendations on CV risk prevention, assessment, monitoring and management during anticancer treatment.
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              The burden of cardiovascular disease in the elderly: morbidity, mortality, and costs.

              Cardiovascular disease (CVD) in older Americans imposes a huge burden in mortality, morbidity, disability, functional decline, and health care costs. In light of the projected growth of the population of older adults over the next several decades, the societal burden attributable to CVD will continue to rise. There is thus an enormous opportunity to foster successful aging and to increase functional life years through expanded efforts aimed at CVD prevention. This article provides an overview of the epidemiology of CVD in older adults, including an assessment of the impact of CVD on mortality, morbidity, and health care costs.
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                Author and article information

                Contributors
                +44 191 2336161 , Chris.Plummer@nhs.net
                Journal
                Blood Cancer J
                Blood Cancer J
                Blood Cancer Journal
                Nature Publishing Group UK (London )
                2044-5385
                26 February 2019
                26 February 2019
                March 2019
                : 9
                : 3
                : 26
                Affiliations
                [1 ]ISNI 0000 0004 0641 3308, GRID grid.415050.5, Department of Cardiology, , Freeman Hospital, ; Freeman Road, Newcastle upon Tyne, NE7 7DN UK
                [2 ]ISNI 0000 0001 2294 4705, GRID grid.413349.8, Department of Oncology and Hematology, , Kantonsspital St Gallen, ; Rorschacher Strasse 95, CH-9007 St Gallen, Switzerland
                [3 ]ISNI 0000 0004 0476 2707, GRID grid.476152.3, Amgen (Europe) GmbH, ; Suurstoffi 22, 6343 Rotkreuz, Switzerland
                [4 ]GRID grid.411258.b, Hematology Service, , University Hospital Salamanca, Casa del Bedel, ; Cardenal Pla y Deniel, 22, Planta Baja, Salamanca, 37008 Spain
                Article
                183
                10.1038/s41408-019-0183-y
                6391463
                30808934
                337c96b8-4fab-459c-8ab0-78feed7c2225
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 21 June 2018
                : 16 November 2018
                : 30 January 2019
                Funding
                Funded by: Amgen (Europe) GmbH
                Categories
                Review Article
                Custom metadata
                © The Author(s) 2019

                Oncology & Radiotherapy
                Oncology & Radiotherapy

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