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Cardiovascular disease after cancer therapy

Improvements in treatment and earlier diagnosis have both contributed to increased survival for many cancer patients. Unfortunately, many treatments carry a risk of late effects including cardiovascular diseases (CVDs), possibly leading to significant morbidity and mortality. In this paper we descri...

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Autores principales: Aleman, Berthe M.P., Moser, Elizabeth C., Nuver, Janine, Suter, Thomas M., Maraldo, Maja V., Specht, Lena, Vrieling, Conny, Darby, Sarah C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250533/
https://www.ncbi.nlm.nih.gov/pubmed/26217163
http://dx.doi.org/10.1016/j.ejcsup.2014.03.002
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author Aleman, Berthe M.P.
Moser, Elizabeth C.
Nuver, Janine
Suter, Thomas M.
Maraldo, Maja V.
Specht, Lena
Vrieling, Conny
Darby, Sarah C.
author_facet Aleman, Berthe M.P.
Moser, Elizabeth C.
Nuver, Janine
Suter, Thomas M.
Maraldo, Maja V.
Specht, Lena
Vrieling, Conny
Darby, Sarah C.
author_sort Aleman, Berthe M.P.
collection PubMed
description Improvements in treatment and earlier diagnosis have both contributed to increased survival for many cancer patients. Unfortunately, many treatments carry a risk of late effects including cardiovascular diseases (CVDs), possibly leading to significant morbidity and mortality. In this paper we describe current knowledge of the cardiotoxicity arising from cancer treatments, outline gaps in knowledge, and indicate directions for future research and guideline development, as discussed during the 2014 Cancer Survivorship Summit organised by the European Organisation for Research and Treatment of Cancer (EORTC). Better knowledge is needed of the late effects of modern systemic treatments and of radiotherapy to critical structures of the heart, including the effect of both radiation dose and volume of the heart exposed. Research elucidating the extent to which treatments interact in causing CVD, and the mechanisms involved, as well as the extent to which treatments may increase CVD indirectly by increasing cardiovascular risk factors is also important. Systematic collection of data relating treatment details to late effects is needed, and great care is needed to obtain valid and generalisable results. Better knowledge of these cardiac effects will contribute to both primary and secondary prevention of late complications where exposure to cardiotoxic treatment is unavoidable. Also surrogate markers would help to identify patients at increased risk of cardiotoxicity. Evidence-based screening guidelines for CVD following cancer are also needed. Finally, risk prediction models should be developed to guide primary treatment choice and appropriate follow up after cancer treatment.
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spelling pubmed-42505332014-12-04 Cardiovascular disease after cancer therapy Aleman, Berthe M.P. Moser, Elizabeth C. Nuver, Janine Suter, Thomas M. Maraldo, Maja V. Specht, Lena Vrieling, Conny Darby, Sarah C. EJC Suppl Article Improvements in treatment and earlier diagnosis have both contributed to increased survival for many cancer patients. Unfortunately, many treatments carry a risk of late effects including cardiovascular diseases (CVDs), possibly leading to significant morbidity and mortality. In this paper we describe current knowledge of the cardiotoxicity arising from cancer treatments, outline gaps in knowledge, and indicate directions for future research and guideline development, as discussed during the 2014 Cancer Survivorship Summit organised by the European Organisation for Research and Treatment of Cancer (EORTC). Better knowledge is needed of the late effects of modern systemic treatments and of radiotherapy to critical structures of the heart, including the effect of both radiation dose and volume of the heart exposed. Research elucidating the extent to which treatments interact in causing CVD, and the mechanisms involved, as well as the extent to which treatments may increase CVD indirectly by increasing cardiovascular risk factors is also important. Systematic collection of data relating treatment details to late effects is needed, and great care is needed to obtain valid and generalisable results. Better knowledge of these cardiac effects will contribute to both primary and secondary prevention of late complications where exposure to cardiotoxic treatment is unavoidable. Also surrogate markers would help to identify patients at increased risk of cardiotoxicity. Evidence-based screening guidelines for CVD following cancer are also needed. Finally, risk prediction models should be developed to guide primary treatment choice and appropriate follow up after cancer treatment. Elsevier 2014-06 2014-05-29 /pmc/articles/PMC4250533/ /pubmed/26217163 http://dx.doi.org/10.1016/j.ejcsup.2014.03.002 Text en © 2014 European Organisation for Research and Treatment of Cancer. Published by Elsevier Limited. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Aleman, Berthe M.P.
Moser, Elizabeth C.
Nuver, Janine
Suter, Thomas M.
Maraldo, Maja V.
Specht, Lena
Vrieling, Conny
Darby, Sarah C.
Cardiovascular disease after cancer therapy
title Cardiovascular disease after cancer therapy
title_full Cardiovascular disease after cancer therapy
title_fullStr Cardiovascular disease after cancer therapy
title_full_unstemmed Cardiovascular disease after cancer therapy
title_short Cardiovascular disease after cancer therapy
title_sort cardiovascular disease after cancer therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4250533/
https://www.ncbi.nlm.nih.gov/pubmed/26217163
http://dx.doi.org/10.1016/j.ejcsup.2014.03.002
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