Immune checkpoint inhibitors (ICIs) are monoclonal antibodies that activate the immune system, aiming at enhancing antitumor immunity. ICIs have shown great promise in the treatment of several advanced malignancies. However, therapy with these immunomodulatory antibodies may lead to a wide spectrum of immune-related adverse events in any organ and any tissue. Cardiologic immune-related events include pericarditis, pericardial effusion, various types of arrhyth-mias including the occurrence of complete atrioventricular block, myocardial infarction, heart fail-ure, and myocarditis. Although relatively rare, myocarditis is associated with a very high reported mortality in comparison to other adverse events. Myocarditis often presents significant diagnostic complexity and may be under-recognized. When confronted with an unexpected change in the clinical picture, the physician must differentiate between immune-related adverse events, cancer wors-ening, or other causes unrelated to the cancer or its therapy. However, this is not always easy. There-fore, with the increasing use of checkpoint inhibitors in cancer, all providers who care for patients with cancer should be made aware of this rare, but potentially fatal, cardiologic immune-related adverse event, and able to recognize when prompt consultation with a cardiologist specialist is in-dicated. In this review, we evaluate currently available scientific evidence and discuss clinical man-ifestations and new potential approaches to the diagnosis and therapy of acute myocarditis induced by ICIs. Temporary or permanent discontinuation of the ICIs and high-dose steroids have been ad-ministered to treat myocarditis, but symptoms may worsen in some patients despite therapy.

An emergent form of cardiotoxicity: Acute myocarditis induced by immune checkpoint inhibitors / Esposito, R.; Fedele, T.; Orefice, S.; Cuomo, V.; Prastaro, M.; Canonico, M. E.; Ilardi, F.; De Stefano, F.; Fiorillo, L.; Santoro, C.; Esposito, G.. - In: BIOMOLECULES. - ISSN 2218-273X. - 11:6(2021), p. 785. [10.3390/biom11060785]

An emergent form of cardiotoxicity: Acute myocarditis induced by immune checkpoint inhibitors

Esposito R.;Fedele T.;Prastaro M.;Canonico M. E.;Ilardi F.;Santoro C.;Esposito G.
2021

Abstract

Immune checkpoint inhibitors (ICIs) are monoclonal antibodies that activate the immune system, aiming at enhancing antitumor immunity. ICIs have shown great promise in the treatment of several advanced malignancies. However, therapy with these immunomodulatory antibodies may lead to a wide spectrum of immune-related adverse events in any organ and any tissue. Cardiologic immune-related events include pericarditis, pericardial effusion, various types of arrhyth-mias including the occurrence of complete atrioventricular block, myocardial infarction, heart fail-ure, and myocarditis. Although relatively rare, myocarditis is associated with a very high reported mortality in comparison to other adverse events. Myocarditis often presents significant diagnostic complexity and may be under-recognized. When confronted with an unexpected change in the clinical picture, the physician must differentiate between immune-related adverse events, cancer wors-ening, or other causes unrelated to the cancer or its therapy. However, this is not always easy. There-fore, with the increasing use of checkpoint inhibitors in cancer, all providers who care for patients with cancer should be made aware of this rare, but potentially fatal, cardiologic immune-related adverse event, and able to recognize when prompt consultation with a cardiologist specialist is in-dicated. In this review, we evaluate currently available scientific evidence and discuss clinical man-ifestations and new potential approaches to the diagnosis and therapy of acute myocarditis induced by ICIs. Temporary or permanent discontinuation of the ICIs and high-dose steroids have been ad-ministered to treat myocarditis, but symptoms may worsen in some patients despite therapy.
2021
An emergent form of cardiotoxicity: Acute myocarditis induced by immune checkpoint inhibitors / Esposito, R.; Fedele, T.; Orefice, S.; Cuomo, V.; Prastaro, M.; Canonico, M. E.; Ilardi, F.; De Stefano, F.; Fiorillo, L.; Santoro, C.; Esposito, G.. - In: BIOMOLECULES. - ISSN 2218-273X. - 11:6(2021), p. 785. [10.3390/biom11060785]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/863395
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