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Cardiotoxicity of tyrosine kinase inhibitors in chronic myelogenous leukemia therapy

Emerging evidence suggests that the three tyrosine kinase inhibitors currently approved for the treatment of patients with chronic myelogenous leukemia (CML) – imatinib, dasatinib, and nilotinib – have potential cardiotoxic effects. The mechanisms behind these events, and the relations between them,...

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Autores principales: Xu, Zhenshu, Cang, Shundong, Yang, Ting, Liu, Delong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3222244/
http://dx.doi.org/10.4081/hr.2009.e4
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author Xu, Zhenshu
Cang, Shundong
Yang, Ting
Liu, Delong
author_facet Xu, Zhenshu
Cang, Shundong
Yang, Ting
Liu, Delong
author_sort Xu, Zhenshu
collection PubMed
description Emerging evidence suggests that the three tyrosine kinase inhibitors currently approved for the treatment of patients with chronic myelogenous leukemia (CML) – imatinib, dasatinib, and nilotinib – have potential cardiotoxic effects. The mechanisms behind these events, and the relations between them, are largely unclear. For example, relative to dasatinib and nilotinib, severe congestive heart failure and left ventricular dysfunction are rare but prominent with imatinib treatment, particularly in patients receiving higher doses (>600 mg/day). In comparison with imatinib, prolongation of the QT interval is relatively common in patients treated with either dasatinib or nilotinib. In contrast to nilotinib, pericardial effusions are observed with both imatinib and dasatinib. It is suggested that these data, an evaluation of cardiac status, use of concomitant medications, and potential risk factors should be considered in the management of CML.
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spelling pubmed-32222442011-12-19 Cardiotoxicity of tyrosine kinase inhibitors in chronic myelogenous leukemia therapy Xu, Zhenshu Cang, Shundong Yang, Ting Liu, Delong Hematol Rev Article Emerging evidence suggests that the three tyrosine kinase inhibitors currently approved for the treatment of patients with chronic myelogenous leukemia (CML) – imatinib, dasatinib, and nilotinib – have potential cardiotoxic effects. The mechanisms behind these events, and the relations between them, are largely unclear. For example, relative to dasatinib and nilotinib, severe congestive heart failure and left ventricular dysfunction are rare but prominent with imatinib treatment, particularly in patients receiving higher doses (>600 mg/day). In comparison with imatinib, prolongation of the QT interval is relatively common in patients treated with either dasatinib or nilotinib. In contrast to nilotinib, pericardial effusions are observed with both imatinib and dasatinib. It is suggested that these data, an evaluation of cardiac status, use of concomitant medications, and potential risk factors should be considered in the management of CML. PAGEPress Publications 2009-03-13 /pmc/articles/PMC3222244/ http://dx.doi.org/10.4081/hr.2009.e4 Text en ©Copyright Z. Xu et al., 2009 This work is licensed under a Creative Commons Attribution 3.0 License (by-nc 3.0). Licensee PAGEPress, Italy
spellingShingle Article
Xu, Zhenshu
Cang, Shundong
Yang, Ting
Liu, Delong
Cardiotoxicity of tyrosine kinase inhibitors in chronic myelogenous leukemia therapy
title Cardiotoxicity of tyrosine kinase inhibitors in chronic myelogenous leukemia therapy
title_full Cardiotoxicity of tyrosine kinase inhibitors in chronic myelogenous leukemia therapy
title_fullStr Cardiotoxicity of tyrosine kinase inhibitors in chronic myelogenous leukemia therapy
title_full_unstemmed Cardiotoxicity of tyrosine kinase inhibitors in chronic myelogenous leukemia therapy
title_short Cardiotoxicity of tyrosine kinase inhibitors in chronic myelogenous leukemia therapy
title_sort cardiotoxicity of tyrosine kinase inhibitors in chronic myelogenous leukemia therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3222244/
http://dx.doi.org/10.4081/hr.2009.e4
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