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Long term adjuvant endocrine therapy and risk of cardiovascular disease in female breast cancer survivors: systematic review

OBJECTIVE: To investigate the effect of endocrine therapies on a wide range of specific clinical cardiovascular disease outcomes in women with a history of non-metastatic breast cancer. DESIGN: Systematic review and meta-analysis of randomised controlled trials and observational studies. DATA SOURCE...

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Autores principales: Matthews, Anthony, Stanway, Susannah, Farmer, Ruth E, Strongman, Helen, Thomas, Sara, Lyon, Alexander R, Smeeth, Liam, Bhaskaran, Krishnan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174332/
https://www.ncbi.nlm.nih.gov/pubmed/30297439
http://dx.doi.org/10.1136/bmj.k3845
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author Matthews, Anthony
Stanway, Susannah
Farmer, Ruth E
Strongman, Helen
Thomas, Sara
Lyon, Alexander R
Smeeth, Liam
Bhaskaran, Krishnan
author_facet Matthews, Anthony
Stanway, Susannah
Farmer, Ruth E
Strongman, Helen
Thomas, Sara
Lyon, Alexander R
Smeeth, Liam
Bhaskaran, Krishnan
author_sort Matthews, Anthony
collection PubMed
description OBJECTIVE: To investigate the effect of endocrine therapies on a wide range of specific clinical cardiovascular disease outcomes in women with a history of non-metastatic breast cancer. DESIGN: Systematic review and meta-analysis of randomised controlled trials and observational studies. DATA SOURCES: Medline and Embase up until June 2018. ELIGIBILITY CRITERIA FOR SELECTING STUDIES: Studies were included if they investigated the risk of a specific cardiovascular disease outcome associated with use of either tamoxifen or an aromatase inhibitor, or compared the two treatments, in women with a history of non-metastatic breast cancer. APPRAISAL AND DATA EXTRACTION: Relevant studies were originally identified and results extracted by one researcher, with a full replication of the study identification process by a combination of two other researchers. The Cochrane Collaboration’s tool for assessing risk of bias was used to assess risk of bias in randomised controlled trials, and this tool was adapted to assess risk of bias in observational studies. RESULTS: 26 studies were identified, with results for seven specific cardiovascular disease outcomes (venous thromboembolism, myocardial infarction, stroke, angina, heart failure, arrhythmia, and peripheral vascular disease). Results suggested an increased risk of venous thromboembolism in tamoxifen users compared with both non-users and aromatase inhibitor users. Results were also consistent with a higher risk of the vascular diseases myocardial infarction and angina in aromatase inhibitor users compared with tamoxifen users, but there was also a suggestion that this may be partly driven by a protective effect of tamoxifen on these outcomes. Data were limited, and evidence was generally inconsistent for all other cardiovascular disease outcomes. CONCLUSION: This review has collated substantial randomised controlled trial and observational evidence on the effect of endocrine therapies on several specific cardiovascular disease outcomes including venous thromboembolism and myocardial infarction, progressing knowledge. Although the choice of aromatase inhibitor or tamoxifen will primarily be based on the effectiveness against the recurrence of breast cancer, this review shows that the individual patient’s risk of venous or arterial vascular disease should be an important secondary consideration. SYSTEMATIC REVIEW REGISTRATION: Prospero CRD42017065944.
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spelling pubmed-61743322018-10-10 Long term adjuvant endocrine therapy and risk of cardiovascular disease in female breast cancer survivors: systematic review Matthews, Anthony Stanway, Susannah Farmer, Ruth E Strongman, Helen Thomas, Sara Lyon, Alexander R Smeeth, Liam Bhaskaran, Krishnan BMJ Research OBJECTIVE: To investigate the effect of endocrine therapies on a wide range of specific clinical cardiovascular disease outcomes in women with a history of non-metastatic breast cancer. DESIGN: Systematic review and meta-analysis of randomised controlled trials and observational studies. DATA SOURCES: Medline and Embase up until June 2018. ELIGIBILITY CRITERIA FOR SELECTING STUDIES: Studies were included if they investigated the risk of a specific cardiovascular disease outcome associated with use of either tamoxifen or an aromatase inhibitor, or compared the two treatments, in women with a history of non-metastatic breast cancer. APPRAISAL AND DATA EXTRACTION: Relevant studies were originally identified and results extracted by one researcher, with a full replication of the study identification process by a combination of two other researchers. The Cochrane Collaboration’s tool for assessing risk of bias was used to assess risk of bias in randomised controlled trials, and this tool was adapted to assess risk of bias in observational studies. RESULTS: 26 studies were identified, with results for seven specific cardiovascular disease outcomes (venous thromboembolism, myocardial infarction, stroke, angina, heart failure, arrhythmia, and peripheral vascular disease). Results suggested an increased risk of venous thromboembolism in tamoxifen users compared with both non-users and aromatase inhibitor users. Results were also consistent with a higher risk of the vascular diseases myocardial infarction and angina in aromatase inhibitor users compared with tamoxifen users, but there was also a suggestion that this may be partly driven by a protective effect of tamoxifen on these outcomes. Data were limited, and evidence was generally inconsistent for all other cardiovascular disease outcomes. CONCLUSION: This review has collated substantial randomised controlled trial and observational evidence on the effect of endocrine therapies on several specific cardiovascular disease outcomes including venous thromboembolism and myocardial infarction, progressing knowledge. Although the choice of aromatase inhibitor or tamoxifen will primarily be based on the effectiveness against the recurrence of breast cancer, this review shows that the individual patient’s risk of venous or arterial vascular disease should be an important secondary consideration. SYSTEMATIC REVIEW REGISTRATION: Prospero CRD42017065944. BMJ Publishing Group Ltd. 2018-10-08 /pmc/articles/PMC6174332/ /pubmed/30297439 http://dx.doi.org/10.1136/bmj.k3845 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research
Matthews, Anthony
Stanway, Susannah
Farmer, Ruth E
Strongman, Helen
Thomas, Sara
Lyon, Alexander R
Smeeth, Liam
Bhaskaran, Krishnan
Long term adjuvant endocrine therapy and risk of cardiovascular disease in female breast cancer survivors: systematic review
title Long term adjuvant endocrine therapy and risk of cardiovascular disease in female breast cancer survivors: systematic review
title_full Long term adjuvant endocrine therapy and risk of cardiovascular disease in female breast cancer survivors: systematic review
title_fullStr Long term adjuvant endocrine therapy and risk of cardiovascular disease in female breast cancer survivors: systematic review
title_full_unstemmed Long term adjuvant endocrine therapy and risk of cardiovascular disease in female breast cancer survivors: systematic review
title_short Long term adjuvant endocrine therapy and risk of cardiovascular disease in female breast cancer survivors: systematic review
title_sort long term adjuvant endocrine therapy and risk of cardiovascular disease in female breast cancer survivors: systematic review
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174332/
https://www.ncbi.nlm.nih.gov/pubmed/30297439
http://dx.doi.org/10.1136/bmj.k3845
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