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Nebivolol effect on doxorubicin-induced cardiotoxicity in breast cancer

PURPOSE: The aim of this study was to assess whether nebivolol treatment could have beneficial effects in the prevention of anthracyclines-induced cardiotoxicity. PATIENTS AND METHODS: Our prospective study included 60 women, mean age 52.6±13 years, with HER2 negative breast cancer, scheduled to und...

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Autores principales: Cochera, Flavia, Dinca, Daniel, Bordejevic, Diana Aurora, Citu, Ioana Mihaela, Mavrea, Adelina Marioara, Andor, Minodora, Trofenciuc, Mihai, Tomescu, Mirela Cleopatra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053261/
https://www.ncbi.nlm.nih.gov/pubmed/30038521
http://dx.doi.org/10.2147/CMAR.S166481
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author Cochera, Flavia
Dinca, Daniel
Bordejevic, Diana Aurora
Citu, Ioana Mihaela
Mavrea, Adelina Marioara
Andor, Minodora
Trofenciuc, Mihai
Tomescu, Mirela Cleopatra
author_facet Cochera, Flavia
Dinca, Daniel
Bordejevic, Diana Aurora
Citu, Ioana Mihaela
Mavrea, Adelina Marioara
Andor, Minodora
Trofenciuc, Mihai
Tomescu, Mirela Cleopatra
author_sort Cochera, Flavia
collection PubMed
description PURPOSE: The aim of this study was to assess whether nebivolol treatment could have beneficial effects in the prevention of anthracyclines-induced cardiotoxicity. PATIENTS AND METHODS: Our prospective study included 60 women, mean age 52.6±13 years, with HER2 negative breast cancer, scheduled to undergo treatment with doxorubicin. The patients were randomly divided into two groups: the treatment group (n=30) which received nebivolol 5 mg once daily for the duration of chemotherapy and the control group (n=30) without treatment with nebivolol. Cytostatic treatment was performed with doxorubicin 70 mg/m(2) administered intravenously every 21 days for six cycles. The average cumulative dose of doxorubicin was 520±8 mg/m(2). Echocardiography was performed immediately before and after six cycles of doxorubicin therapy. RESULTS: We found no significant differences between the two groups regarding baseline clinical and echocardiographic parameters. The two groups reached a similar cumulative dose of doxorubicin. No patient died during the study. None of the patients withdrew from chemotherapy. After six cycles of doxorubicin therapy, the left ventricular (LV) ejection fraction, shortening fraction, and LV diameters changed, but not significantly. Tissue Doppler imaging (TDI) detected in the control group a significant decrease of myocardial velocities, indicating a LV diastolic dysfunction. In the same group, speckle tracking imaging (STI) revealed a statistically significant alteration of the ventricular deformation, which means a decrease in LV systolic function. In the nebivolol treatment group, no significant alterations in the LV systolic and diastolic function were observed. CONCLUSION: The results of this study show the benefit of new echocardiographic imaging methods such as TDI and STI in the screening of early cardiac dysfunction induced by cytostatic treatment. Nebivolol treatment prevented the occurrence of anthracyclines-induced cardiomyopathy in the short term. In order to confirm these preliminary results, larger studies with a longer follow-up period are required.
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spelling pubmed-60532612018-07-23 Nebivolol effect on doxorubicin-induced cardiotoxicity in breast cancer Cochera, Flavia Dinca, Daniel Bordejevic, Diana Aurora Citu, Ioana Mihaela Mavrea, Adelina Marioara Andor, Minodora Trofenciuc, Mihai Tomescu, Mirela Cleopatra Cancer Manag Res Original Research PURPOSE: The aim of this study was to assess whether nebivolol treatment could have beneficial effects in the prevention of anthracyclines-induced cardiotoxicity. PATIENTS AND METHODS: Our prospective study included 60 women, mean age 52.6±13 years, with HER2 negative breast cancer, scheduled to undergo treatment with doxorubicin. The patients were randomly divided into two groups: the treatment group (n=30) which received nebivolol 5 mg once daily for the duration of chemotherapy and the control group (n=30) without treatment with nebivolol. Cytostatic treatment was performed with doxorubicin 70 mg/m(2) administered intravenously every 21 days for six cycles. The average cumulative dose of doxorubicin was 520±8 mg/m(2). Echocardiography was performed immediately before and after six cycles of doxorubicin therapy. RESULTS: We found no significant differences between the two groups regarding baseline clinical and echocardiographic parameters. The two groups reached a similar cumulative dose of doxorubicin. No patient died during the study. None of the patients withdrew from chemotherapy. After six cycles of doxorubicin therapy, the left ventricular (LV) ejection fraction, shortening fraction, and LV diameters changed, but not significantly. Tissue Doppler imaging (TDI) detected in the control group a significant decrease of myocardial velocities, indicating a LV diastolic dysfunction. In the same group, speckle tracking imaging (STI) revealed a statistically significant alteration of the ventricular deformation, which means a decrease in LV systolic function. In the nebivolol treatment group, no significant alterations in the LV systolic and diastolic function were observed. CONCLUSION: The results of this study show the benefit of new echocardiographic imaging methods such as TDI and STI in the screening of early cardiac dysfunction induced by cytostatic treatment. Nebivolol treatment prevented the occurrence of anthracyclines-induced cardiomyopathy in the short term. In order to confirm these preliminary results, larger studies with a longer follow-up period are required. Dove Medical Press 2018-07-16 /pmc/articles/PMC6053261/ /pubmed/30038521 http://dx.doi.org/10.2147/CMAR.S166481 Text en © 2018 Cochera et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Cochera, Flavia
Dinca, Daniel
Bordejevic, Diana Aurora
Citu, Ioana Mihaela
Mavrea, Adelina Marioara
Andor, Minodora
Trofenciuc, Mihai
Tomescu, Mirela Cleopatra
Nebivolol effect on doxorubicin-induced cardiotoxicity in breast cancer
title Nebivolol effect on doxorubicin-induced cardiotoxicity in breast cancer
title_full Nebivolol effect on doxorubicin-induced cardiotoxicity in breast cancer
title_fullStr Nebivolol effect on doxorubicin-induced cardiotoxicity in breast cancer
title_full_unstemmed Nebivolol effect on doxorubicin-induced cardiotoxicity in breast cancer
title_short Nebivolol effect on doxorubicin-induced cardiotoxicity in breast cancer
title_sort nebivolol effect on doxorubicin-induced cardiotoxicity in breast cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053261/
https://www.ncbi.nlm.nih.gov/pubmed/30038521
http://dx.doi.org/10.2147/CMAR.S166481
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