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Baseline blood pressure and development of cardiotoxicity in patients treated with anthracyclines: A systematic review

AIMS: Anthracyclines, a mainstay of cancer treatment, are associated with significant life-threatening cardiotoxicity. As cancer survivorship improves, there is a growing need to identify patients most at risk and strategies to mitigate anthracycline-associated cardiotoxicity. Elevated baseline bloo...

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Autores principales: Philip, Laura J., Findlay, Simon G., Gill, Jason H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789356/
https://www.ncbi.nlm.nih.gov/pubmed/36573186
http://dx.doi.org/10.1016/j.ijcrp.2022.200153
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author Philip, Laura J.
Findlay, Simon G.
Gill, Jason H.
author_facet Philip, Laura J.
Findlay, Simon G.
Gill, Jason H.
author_sort Philip, Laura J.
collection PubMed
description AIMS: Anthracyclines, a mainstay of cancer treatment, are associated with significant life-threatening cardiotoxicity. As cancer survivorship improves, there is a growing need to identify patients most at risk and strategies to mitigate anthracycline-associated cardiotoxicity. Elevated baseline blood pressure (bBP) is a possible risk factor for cardiotoxicity. The aim of this systematic review was to summarise the literature and evaluate relationships between bBP and anthracycline-associated cardiotoxicity. METHODS AND RESULTS: Systematic searches were conducted, limited to English language but without restrictions on study type or country of origin. All studies fulfilled the PRISMA statement and relevant studies reviewed and narratively synthesised. A total of 1330 papers were screened, with 12 included in the qualitative synthesis. Eight papers indicated elevated bBP was associated with significantly higher risk of developing cardiotoxicity. Four papers noted significant relationships between left ventricular ejection fraction (LVEF) decline and elevated bBP. Of the four papers that failed to show an association, one noted increased risk of developing chronic heart failure. A relationship between baseline diastolic and systolic BP and anthracycline-associated cardiotoxicity is also noted. CONCLUSIONS: This study indicates adult patients with elevated bBP have increased vulnerability to anthracycline-associated cardiotoxicity, with those with pre-hypertension or raised systolic versus diastolic pressure potentially an overlooked population. Recommendations for inclusion of bBP, incorporating individual systolic versus diastolic pressures, in cardio-oncology risk prediction models to guide clinical decision-making are thus warranted.
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spelling pubmed-97893562022-12-25 Baseline blood pressure and development of cardiotoxicity in patients treated with anthracyclines: A systematic review Philip, Laura J. Findlay, Simon G. Gill, Jason H. Int J Cardiol Cardiovasc Risk Prev Research Paper AIMS: Anthracyclines, a mainstay of cancer treatment, are associated with significant life-threatening cardiotoxicity. As cancer survivorship improves, there is a growing need to identify patients most at risk and strategies to mitigate anthracycline-associated cardiotoxicity. Elevated baseline blood pressure (bBP) is a possible risk factor for cardiotoxicity. The aim of this systematic review was to summarise the literature and evaluate relationships between bBP and anthracycline-associated cardiotoxicity. METHODS AND RESULTS: Systematic searches were conducted, limited to English language but without restrictions on study type or country of origin. All studies fulfilled the PRISMA statement and relevant studies reviewed and narratively synthesised. A total of 1330 papers were screened, with 12 included in the qualitative synthesis. Eight papers indicated elevated bBP was associated with significantly higher risk of developing cardiotoxicity. Four papers noted significant relationships between left ventricular ejection fraction (LVEF) decline and elevated bBP. Of the four papers that failed to show an association, one noted increased risk of developing chronic heart failure. A relationship between baseline diastolic and systolic BP and anthracycline-associated cardiotoxicity is also noted. CONCLUSIONS: This study indicates adult patients with elevated bBP have increased vulnerability to anthracycline-associated cardiotoxicity, with those with pre-hypertension or raised systolic versus diastolic pressure potentially an overlooked population. Recommendations for inclusion of bBP, incorporating individual systolic versus diastolic pressures, in cardio-oncology risk prediction models to guide clinical decision-making are thus warranted. Elsevier 2022-10-13 /pmc/articles/PMC9789356/ /pubmed/36573186 http://dx.doi.org/10.1016/j.ijcrp.2022.200153 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Philip, Laura J.
Findlay, Simon G.
Gill, Jason H.
Baseline blood pressure and development of cardiotoxicity in patients treated with anthracyclines: A systematic review
title Baseline blood pressure and development of cardiotoxicity in patients treated with anthracyclines: A systematic review
title_full Baseline blood pressure and development of cardiotoxicity in patients treated with anthracyclines: A systematic review
title_fullStr Baseline blood pressure and development of cardiotoxicity in patients treated with anthracyclines: A systematic review
title_full_unstemmed Baseline blood pressure and development of cardiotoxicity in patients treated with anthracyclines: A systematic review
title_short Baseline blood pressure and development of cardiotoxicity in patients treated with anthracyclines: A systematic review
title_sort baseline blood pressure and development of cardiotoxicity in patients treated with anthracyclines: a systematic review
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9789356/
https://www.ncbi.nlm.nih.gov/pubmed/36573186
http://dx.doi.org/10.1016/j.ijcrp.2022.200153
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