| Literature DB >> 27866063 |
Daniela Di Lisi1, Rosalinda Madonna2, Concetta Zito3, Enrico Bronte4, Giuseppe Badalamenti4, Paolo Parrella5, Ines Monte6, Carlo Gabriele Tocchetti5, Antonio Russo4, Giuseppina Novo1.
Abstract
Cardiotoxicity induced by chemotherapeutic agents and radiotherapy is a growing problem. In recent years, an increasing number of new drugs with targeted action have been designed. These molecules, such as monoclonal antibodies and tyrosine kinase inhibitors, can cause different type of toxicities compared to traditional chemotherapy. However, they can also cause cardiac complications such as heart failure, arterial hypertension, QT interval prolongation and arrhythmias. Currently, a field of intense research is the vascular toxicity induced by new biologic drugs, particularly those which inhibit vascular endothelial growth factor (VEGF) and its receptor (VEGF-R) and other tyrosine kinases. In this review, we aim at focusing on the problem of vascular toxicity induced by new targeted therapies, chemotherapy and radiotherapy, and describe the main mechanisms and emphasizing the importance of early diagnosis of vascular damage, in order to prevent clinical complications.Entities:
Keywords: Cardio-oncology; Cardiotoxicity; Chemotherapy; New target therapy; Radiotherapy; VEGF; Vascular toxicity
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Year: 2016 PMID: 27866063 DOI: 10.1016/j.ijcard.2016.11.174
Source DB: PubMed Journal: Int J Cardiol ISSN: 0167-5273 Impact factor: 4.164