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Baseline global longitudinal strain predictive of anthracycline-induced cardiotoxicity

BACKGROUND: Cancer therapy-related cardiac dysfunction (CTRD) is a major source of morbidity and mortality in long-term cancer survivors. Decreased GLS predicts decreased left ventricular ejection fraction (LVEF) in patients receiving anthracyclines, but knowledge regarding the clinical utility of b...

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Autores principales: Araujo-Gutierrez, Raquel, Chitturi, Kalyan R., Xu, Jiaqiong, Wang, Yuanchen, Kinder, Elizabeth, Senapati, Alpana, Chebrolu, L. Bindu, Kassi, Mahwash, Trachtenberg, Barry H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849080/
https://www.ncbi.nlm.nih.gov/pubmed/33517910
http://dx.doi.org/10.1186/s40959-021-00090-2
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author Araujo-Gutierrez, Raquel
Chitturi, Kalyan R.
Xu, Jiaqiong
Wang, Yuanchen
Kinder, Elizabeth
Senapati, Alpana
Chebrolu, L. Bindu
Kassi, Mahwash
Trachtenberg, Barry H.
author_facet Araujo-Gutierrez, Raquel
Chitturi, Kalyan R.
Xu, Jiaqiong
Wang, Yuanchen
Kinder, Elizabeth
Senapati, Alpana
Chebrolu, L. Bindu
Kassi, Mahwash
Trachtenberg, Barry H.
author_sort Araujo-Gutierrez, Raquel
collection PubMed
description BACKGROUND: Cancer therapy-related cardiac dysfunction (CTRD) is a major source of morbidity and mortality in long-term cancer survivors. Decreased GLS predicts decreased left ventricular ejection fraction (LVEF) in patients receiving anthracyclines, but knowledge regarding the clinical utility of baseline GLS in patients at low-risk of (CTRD) is limited. OBJECTIVES: The purpose of this study was to investigate whether baseline echocardiographic assessment of global longitudinal strain (GLS) before treatment with anthracyclines is predictive of (CTRD) in a broad cohort of patients with normal baseline LVEF. METHODS: Study participants comprised 188 patients at a single institution who underwent baseline 2-dimensional (2D) speckle-tracking echocardiography before treatment with anthracyclines and at least one follow-up echocardiogram 3 months after chemotherapy initiation. Patients with a baseline LVEF <55% were excluded from the analysis. The primary endpoint, (CTRD), was defined as an absolute decline in LVEF > 10% from baseline and an overall reduced LVEF <50%. Potential and known risk factors were evaluated using univariable and multivariable Cox proportional hazards regression analysis. RESULTS: Twenty-three patients (12.23%) developed (CTRD). Among patients with (CTRD), the mean GLS was -17.51% ± 2.77%. The optimal cutoff point for (CTRD) was -18.05%. The sensitivity was 0.70 and specificity was 0.70. The area under ROC curve was 0.70. After adjustment for cardiovascular and cancer therapy related risk factors, GLS or decreased baseline GLS ≥-18% was predictive of (CTRD) (adjusted hazards ratio 1.17, 95% confidence interval 1.00, 1.36; p = 0.044 for GLS, or hazards ratio 3.54; 95% confidence interval 1.34, 9.35; p = 0.011 for decreased GLS), along with history of tobacco use, pre-chemotherapy systolic blood pressure, and cumulative anthracycline dose. CONCLUSIONS: Baseline GLS or decreased baseline GLS was predictive of (CTRD) before anthracycline treatment in a cohort of cancer patients with a normal baseline LVEF. This data supports the implementation of strain-protocol echocardiography in cardio-oncology practice for identifying and monitoring patients who are at elevated risk of (CTRD).
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spelling pubmed-78490802021-02-03 Baseline global longitudinal strain predictive of anthracycline-induced cardiotoxicity Araujo-Gutierrez, Raquel Chitturi, Kalyan R. Xu, Jiaqiong Wang, Yuanchen Kinder, Elizabeth Senapati, Alpana Chebrolu, L. Bindu Kassi, Mahwash Trachtenberg, Barry H. Cardiooncology Research BACKGROUND: Cancer therapy-related cardiac dysfunction (CTRD) is a major source of morbidity and mortality in long-term cancer survivors. Decreased GLS predicts decreased left ventricular ejection fraction (LVEF) in patients receiving anthracyclines, but knowledge regarding the clinical utility of baseline GLS in patients at low-risk of (CTRD) is limited. OBJECTIVES: The purpose of this study was to investigate whether baseline echocardiographic assessment of global longitudinal strain (GLS) before treatment with anthracyclines is predictive of (CTRD) in a broad cohort of patients with normal baseline LVEF. METHODS: Study participants comprised 188 patients at a single institution who underwent baseline 2-dimensional (2D) speckle-tracking echocardiography before treatment with anthracyclines and at least one follow-up echocardiogram 3 months after chemotherapy initiation. Patients with a baseline LVEF <55% were excluded from the analysis. The primary endpoint, (CTRD), was defined as an absolute decline in LVEF > 10% from baseline and an overall reduced LVEF <50%. Potential and known risk factors were evaluated using univariable and multivariable Cox proportional hazards regression analysis. RESULTS: Twenty-three patients (12.23%) developed (CTRD). Among patients with (CTRD), the mean GLS was -17.51% ± 2.77%. The optimal cutoff point for (CTRD) was -18.05%. The sensitivity was 0.70 and specificity was 0.70. The area under ROC curve was 0.70. After adjustment for cardiovascular and cancer therapy related risk factors, GLS or decreased baseline GLS ≥-18% was predictive of (CTRD) (adjusted hazards ratio 1.17, 95% confidence interval 1.00, 1.36; p = 0.044 for GLS, or hazards ratio 3.54; 95% confidence interval 1.34, 9.35; p = 0.011 for decreased GLS), along with history of tobacco use, pre-chemotherapy systolic blood pressure, and cumulative anthracycline dose. CONCLUSIONS: Baseline GLS or decreased baseline GLS was predictive of (CTRD) before anthracycline treatment in a cohort of cancer patients with a normal baseline LVEF. This data supports the implementation of strain-protocol echocardiography in cardio-oncology practice for identifying and monitoring patients who are at elevated risk of (CTRD). BioMed Central 2021-01-31 /pmc/articles/PMC7849080/ /pubmed/33517910 http://dx.doi.org/10.1186/s40959-021-00090-2 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Araujo-Gutierrez, Raquel
Chitturi, Kalyan R.
Xu, Jiaqiong
Wang, Yuanchen
Kinder, Elizabeth
Senapati, Alpana
Chebrolu, L. Bindu
Kassi, Mahwash
Trachtenberg, Barry H.
Baseline global longitudinal strain predictive of anthracycline-induced cardiotoxicity
title Baseline global longitudinal strain predictive of anthracycline-induced cardiotoxicity
title_full Baseline global longitudinal strain predictive of anthracycline-induced cardiotoxicity
title_fullStr Baseline global longitudinal strain predictive of anthracycline-induced cardiotoxicity
title_full_unstemmed Baseline global longitudinal strain predictive of anthracycline-induced cardiotoxicity
title_short Baseline global longitudinal strain predictive of anthracycline-induced cardiotoxicity
title_sort baseline global longitudinal strain predictive of anthracycline-induced cardiotoxicity
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849080/
https://www.ncbi.nlm.nih.gov/pubmed/33517910
http://dx.doi.org/10.1186/s40959-021-00090-2
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