| Literature DB >> 32026180 |
Grazia Casavecchia1, Maurizio Galderisi2, Giuseppina Novo3, Matteo Gravina1, Ciro Santoro2, Eustachio Agricola4, Silvana Capalbo1, Stefano Zicchino5, Matteo Cameli6, Luisa De Gennaro7, Francesca Maria Righini6, Ines Monte8, Carlo Gabriele Tocchetti9, Natale Daniele Brunetti10, Cristian Cadeddu11, Giuseppe Mercuro11.
Abstract
Chronic myeloid leukemia (CML) is a myeloproliferative disorder characterized by neoplastic transformation of pluripotent cells due to a typical cytogenetic and molecular mutation known as Philadelphia (Ph) chromosome. In 2001, the introduction of the tyrosine kinasis inhibitor (TKI) imatinib as a therapeutic strategy for CML with PH chromosome mutation represented an important step towards treatment of these patients, and nowadays, this drug represents the gold therapeutic standard in this clinical setting. A second generation of TKIs (dasatinib, nilotinib, and bosutinib) showed an effective action in all patients with mutations resistant to imatinib. Ponatinib is a third-generation TKI and is the only inhibitor with activity against T3151 mutation. The impact of ponatinib on cardiovascular events was first evaluated in the PACE trial. We therefore report and discuss most relevant evidence currently available on cardiovascular events associated with the use of ponatinib. Though many exams can be used for diagnosis and follow-up of this kind of cardiotoxicity, echocardiography seems to have a pivotal role thanks to its feasibility, availability, and low cost.Entities:
Keywords: Cardio-oncology; Chronic myeloid leukemia; Ponatinib; Review; Tyrosine kinase inhibitors
Year: 2020 PMID: 32026180 DOI: 10.1007/s10741-020-09926-y
Source DB: PubMed Journal: Heart Fail Rev ISSN: 1382-4147 Impact factor: 4.214