Key result
Cardiac involvement in hematologic malignancies arises from myocardial infiltration or chemotherapy toxicity, ranging from subclinical abnormalities to life-threatening events.
This review emphasizes the importance of recognizing and managing cardiac involvement and chemotherapy-induced cardiotoxicity in patients with hematologic malignancies.
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Alerts clinicians to monitor for cardiac complications in hematologic malignancy patients; leaves open optimal surveillance strategies.
Authors have reviewed literature about the management of patients with cardiologic disease occurring secondary to hematologic pathology itself or its therapy, with a focus on infiltration of myocardium in acute and chronic leukemia, lymphoma, multiple myeloma, and hypereosinophilic syndrome. Moreover, they evaluated chemotherapy-associated toxicity, particularly for new drugs such as monoclonal antibody therapy, tyrosine kinase inhibitors, arsenic trioxide, bortezomib, and epigenetic therapy. In fact, cardiac toxicity may range from asymptomatic subclinical abnormalities, such as electrocardiographic changes and left ventricular ejection decline, to life-threatening events and lead to chemotherapy dose reduction and delay and, in some cases, for patients with severe side effects, discontinuation of treatment. Finally, they discussed on the identification of early markers of cardiac injury and on cardiac stem cell therapy as a promising approach to facilitate myocardial regeneration.
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Allegra et al. (2010) conducted a review in Hematologic malignancies with cardiac involvement. Hematologic malignancies and associated therapies was evaluated. Cardiac involvement in hematologic malignancies arises from myocardial infiltration or chemotherapy toxicity, ranging from subclinical abnormalities to life-threatening events.
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