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Longitudinal Strain and Troponin I Elevation in Patients Undergoing Immune Checkpoint Inhibitor Therapy

BACKGROUND: Immune checkpoint inhibitors (ICIs) are a central part of cancer therapy; however, cardiac complications, such as myocarditis, have the potential for significant morbidity and mortality. Within this population, the clinical significance of longitudinal strain (LS) remains unknown. OBJECT...

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Autores principales: Tamura, Yudai, Tamura, Yuichi, Takemura, Ryo, Yamada, Kenta, Taniguchi, Hirohisa, Iwasawa, Jin, Yada, Hirotaka, Kawamura, Akio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830215/
https://www.ncbi.nlm.nih.gov/pubmed/36636435
http://dx.doi.org/10.1016/j.jaccao.2022.10.007
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author Tamura, Yudai
Tamura, Yuichi
Takemura, Ryo
Yamada, Kenta
Taniguchi, Hirohisa
Iwasawa, Jin
Yada, Hirotaka
Kawamura, Akio
author_facet Tamura, Yudai
Tamura, Yuichi
Takemura, Ryo
Yamada, Kenta
Taniguchi, Hirohisa
Iwasawa, Jin
Yada, Hirotaka
Kawamura, Akio
author_sort Tamura, Yudai
collection PubMed
description BACKGROUND: Immune checkpoint inhibitors (ICIs) are a central part of cancer therapy; however, cardiac complications, such as myocarditis, have the potential for significant morbidity and mortality. Within this population, the clinical significance of longitudinal strain (LS) remains unknown. OBJECTIVES: This study sought to define the changes in LS in ICI-treated patients, and their associations with high-sensitivity troponin I (hsTnI) and myocarditis. METHODS: We conducted a retrospective cohort study of patients who received ICIs at our hospital from April 2017 to September 2021. All patients underwent echocardiography and blood sampling at standardized time intervals. We measured the changes in global and regional LS before and after ICI administration. Age- and sex-adjusted Cox regression analysis was used to evaluate the association between LS and elevations in hsTnI and myocarditis. RESULTS: In a cohort of 129 patients with a median follow-up period of 170 (IQR: 62-365) days; 6 and 18 patients had myocarditis and hsTnI elevation, respectively. In an age- and sex-adjusted Cox proportional hazards model, an early relative worsening of ≥10% in the basal and mid LS and ≥15% in global LS was associated with hsTnI elevation. Relative reductions in LS were not significantly associated with myocarditis; however, 4 of the 6 patients with myocarditis had relative reduction of ≥10% in the basal LS. CONCLUSIONS: An early worsening in the global and regional LS was associated with increased hsTnI in patients receiving ICIs. Assessment of LS early after ICI administration should be further studied as a strategy for risk stratification of ICI-treated patients.
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spelling pubmed-98302152023-01-11 Longitudinal Strain and Troponin I Elevation in Patients Undergoing Immune Checkpoint Inhibitor Therapy Tamura, Yudai Tamura, Yuichi Takemura, Ryo Yamada, Kenta Taniguchi, Hirohisa Iwasawa, Jin Yada, Hirotaka Kawamura, Akio JACC CardioOncol Original Research BACKGROUND: Immune checkpoint inhibitors (ICIs) are a central part of cancer therapy; however, cardiac complications, such as myocarditis, have the potential for significant morbidity and mortality. Within this population, the clinical significance of longitudinal strain (LS) remains unknown. OBJECTIVES: This study sought to define the changes in LS in ICI-treated patients, and their associations with high-sensitivity troponin I (hsTnI) and myocarditis. METHODS: We conducted a retrospective cohort study of patients who received ICIs at our hospital from April 2017 to September 2021. All patients underwent echocardiography and blood sampling at standardized time intervals. We measured the changes in global and regional LS before and after ICI administration. Age- and sex-adjusted Cox regression analysis was used to evaluate the association between LS and elevations in hsTnI and myocarditis. RESULTS: In a cohort of 129 patients with a median follow-up period of 170 (IQR: 62-365) days; 6 and 18 patients had myocarditis and hsTnI elevation, respectively. In an age- and sex-adjusted Cox proportional hazards model, an early relative worsening of ≥10% in the basal and mid LS and ≥15% in global LS was associated with hsTnI elevation. Relative reductions in LS were not significantly associated with myocarditis; however, 4 of the 6 patients with myocarditis had relative reduction of ≥10% in the basal LS. CONCLUSIONS: An early worsening in the global and regional LS was associated with increased hsTnI in patients receiving ICIs. Assessment of LS early after ICI administration should be further studied as a strategy for risk stratification of ICI-treated patients. Elsevier 2022-12-20 /pmc/articles/PMC9830215/ /pubmed/36636435 http://dx.doi.org/10.1016/j.jaccao.2022.10.007 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 Original Research
Tamura, Yudai
Tamura, Yuichi
Takemura, Ryo
Yamada, Kenta
Taniguchi, Hirohisa
Iwasawa, Jin
Yada, Hirotaka
Kawamura, Akio
Longitudinal Strain and Troponin I Elevation in Patients Undergoing Immune Checkpoint Inhibitor Therapy
title Longitudinal Strain and Troponin I Elevation in Patients Undergoing Immune Checkpoint Inhibitor Therapy
title_full Longitudinal Strain and Troponin I Elevation in Patients Undergoing Immune Checkpoint Inhibitor Therapy
title_fullStr Longitudinal Strain and Troponin I Elevation in Patients Undergoing Immune Checkpoint Inhibitor Therapy
title_full_unstemmed Longitudinal Strain and Troponin I Elevation in Patients Undergoing Immune Checkpoint Inhibitor Therapy
title_short Longitudinal Strain and Troponin I Elevation in Patients Undergoing Immune Checkpoint Inhibitor Therapy
title_sort longitudinal strain and troponin i elevation in patients undergoing immune checkpoint inhibitor therapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830215/
https://www.ncbi.nlm.nih.gov/pubmed/36636435
http://dx.doi.org/10.1016/j.jaccao.2022.10.007
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