Cardiac toxicities in multiple myeloma: an updated and a deeper look into the effect of different medications and novel therapies

Abstract

With the continuous improvement in survival of cancer patients, including those with multiple myeloma, related to the novel treatment agents and therapeutic approaches, the probability for patients to develop cardiovascular disease has significantly increased, especially in elderly patients and those with additional risk factors. Multiple myeloma is indeed a disease of the elderly population and so these patients are, solely by age, at an increased risk of cardiovascular disease. Risk factors for these events can be patient-, disease- and/or therapy-related, and they have been shown to adversely impact survival. Cardiovascular events affect around 7.5% of patients with multiple myeloma and the risk for different toxicities has considerably varied across trials depending on patients’ characteristics and treatment utilized. High grade cardiac toxicity has been reported with immunomodulatory drugs (odds ratio [OR] around 2), proteasome inhibitors (OR 1.67–2.68 depending on the specific agent, and generally higher with carfilzomib), as well as other agents. Cardiac arrhythmias have also been reported with various therapies and drug interaction plays a significant role in that setting. Comprehensive cardiac evaluation before, during and after various anti-myeloma therapy is recommended and the incorporation of surveillance strategies allows early detection and management resulting in improved outcomes of these patients. Multidisciplinary interaction including hematologists and cardio-oncologists is critical for optimal patient care. © 2023, The Author(s).

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Keywords

Aged, Cardiotoxicity, Cardiovascular diseases, Humans, Multiple myeloma, Proteasome inhibitors, Risk factors, Adp ribosyl cyclase/cyclic adp ribose hydrolase 1, Antineoplastic monoclonal antibody, Bispecific antibody, Cell therapy agent, Elotuzumab, Immunomodulating agent, Proteasome inhibitor, Cancer chemotherapy, Cancer immunotherapy, Cardiovascular risk, Chimeric antigen receptor t-cell immunotherapy, Disease risk assessment, Human, Patient monitoring, Review, Cardiovascular disease, Complication, Risk factor

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