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Int J Mol Sci ; 23(18)2022 Sep 19.
Article in English | MEDLINE | ID: mdl-36142866

ABSTRACT

Immune checkpoint inhibitors (ICIs) are an important advancement in the field of cancer treatment, significantly improving the survival of patients with a series of advanced malignancies, like melanoma, non-small cell lung cancer (NSCLC), hepatocellular carcinoma (HCC), renal cell carcinoma (RCC), and Hodgkin lymphoma. ICIs act upon T lymphocytes and antigen-presenting cells, targeting programmed cell death protein 1 (PD1), programmed cell death protein ligand 1 (PD-L1), and cytotoxic T-lymphocyte antigen 4 (CTLA-4), breaking the immune tolerance of the T cells against malignant cells and enhancing the body's own immune response. A variety of cardiac-adverse effects are associated with ICI-based treatment, including pericarditis, arrhythmias, cardiomyopathy, and acute coronary syndrome, with myocarditis being the most studied due to its often-unexpected onset and severity. Overall, Myocarditis is rare but presents an immune-related adverse event (irAE) that has a high fatality rate. Considering the rising number of oncological patients treated with ICIs and the severity of their potential adverse effects, a good understanding and continuous investigation of cardiac irAEs is of the utmost importance. This systematic review aimed to revise recent publications (between 2016-2022) on ICI-induced cardiac toxicities and highlight the therapeutical approach and evolution in the selected cases.


Subject(s)
Antineoplastic Agents, Immunological , Carcinoma, Hepatocellular , Carcinoma, Non-Small-Cell Lung , Drug-Related Side Effects and Adverse Reactions , Liver Neoplasms , Lung Neoplasms , Myocarditis , Antineoplastic Agents, Immunological/therapeutic use , Apoptosis Regulatory Proteins , B7-H1 Antigen , CTLA-4 Antigen , Carcinoma, Hepatocellular/chemically induced , Carcinoma, Non-Small-Cell Lung/drug therapy , Cardiotoxicity/etiology , Humans , Immune Checkpoint Inhibitors/adverse effects , Ligands , Liver Neoplasms/chemically induced , Lung Neoplasms/drug therapy , Myocarditis/chemically induced , Programmed Cell Death 1 Receptor
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