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Cardiac events during treatment with proteasome inhibitor therapy for multiple myeloma

BACKGROUND: Proteasome inhibitors (PI) bortezomib and carfilzomib are cornerstone therapies for multiple myeloma. Higher incidence of cardiac adverse events (CAEs) has been reported in patients receiving carfilzomib. However, risk factors for cardiac toxicity remain unclear. Our objective was to eva...

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Autores principales: Chen, John H., Lenihan, Daniel J., Phillips, Sharon E., Harrell, Shelton L., Cornell, Robert F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048104/
https://www.ncbi.nlm.nih.gov/pubmed/32154000
http://dx.doi.org/10.1186/s40959-017-0023-9
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author Chen, John H.
Lenihan, Daniel J.
Phillips, Sharon E.
Harrell, Shelton L.
Cornell, Robert F.
author_facet Chen, John H.
Lenihan, Daniel J.
Phillips, Sharon E.
Harrell, Shelton L.
Cornell, Robert F.
author_sort Chen, John H.
collection PubMed
description BACKGROUND: Proteasome inhibitors (PI) bortezomib and carfilzomib are cornerstone therapies for multiple myeloma. Higher incidence of cardiac adverse events (CAEs) has been reported in patients receiving carfilzomib. However, risk factors for cardiac toxicity remain unclear. Our objective was to evaluate the incidence of CAEs associated with PI and recognize risk factors for developing events. METHODS: This was a descriptive analysis of 96 patients with multiple myeloma who received bortezomib (n = 44) or carfilzomib (n = 52). We compared the cumulative incidence of CAEs using a log rank test. Patient-related characteristics were assessed and multivariate analysis was used to identify risk factors for developing CAEs. RESULTS: PI-related CAEs occurred in 21 (22%) patients. Bortezomib-associated CAEs occurred in 7 (16%) patients while carfilzomib-associated cardiac events occurred in 14 (27%) patients. The cumulative incidence of CAEs was not significantly different between agents. Events occurred after a median of 67.5 days on PI therapy. Heart failure was the most prevalent event type. More patients receiving carfilzomib were monitored by a cardiologist. By multivariate analysis, a history of prior cardiac events and longer duration of PI therapy were identified as independent risk factors for developing CAEs. CONCLUSIONS: AEs were common in patients receiving PIs. Choice of PI did not impact the cumulative incidence of CAEs. Early involvement by a cardiologist in patients at high risk for CAEs may help to mitigate the frequency and severity of CAEs.
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spelling pubmed-70481042020-03-09 Cardiac events during treatment with proteasome inhibitor therapy for multiple myeloma Chen, John H. Lenihan, Daniel J. Phillips, Sharon E. Harrell, Shelton L. Cornell, Robert F. Cardiooncology Research BACKGROUND: Proteasome inhibitors (PI) bortezomib and carfilzomib are cornerstone therapies for multiple myeloma. Higher incidence of cardiac adverse events (CAEs) has been reported in patients receiving carfilzomib. However, risk factors for cardiac toxicity remain unclear. Our objective was to evaluate the incidence of CAEs associated with PI and recognize risk factors for developing events. METHODS: This was a descriptive analysis of 96 patients with multiple myeloma who received bortezomib (n = 44) or carfilzomib (n = 52). We compared the cumulative incidence of CAEs using a log rank test. Patient-related characteristics were assessed and multivariate analysis was used to identify risk factors for developing CAEs. RESULTS: PI-related CAEs occurred in 21 (22%) patients. Bortezomib-associated CAEs occurred in 7 (16%) patients while carfilzomib-associated cardiac events occurred in 14 (27%) patients. The cumulative incidence of CAEs was not significantly different between agents. Events occurred after a median of 67.5 days on PI therapy. Heart failure was the most prevalent event type. More patients receiving carfilzomib were monitored by a cardiologist. By multivariate analysis, a history of prior cardiac events and longer duration of PI therapy were identified as independent risk factors for developing CAEs. CONCLUSIONS: AEs were common in patients receiving PIs. Choice of PI did not impact the cumulative incidence of CAEs. Early involvement by a cardiologist in patients at high risk for CAEs may help to mitigate the frequency and severity of CAEs. BioMed Central 2017-06-01 /pmc/articles/PMC7048104/ /pubmed/32154000 http://dx.doi.org/10.1186/s40959-017-0023-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research
Chen, John H.
Lenihan, Daniel J.
Phillips, Sharon E.
Harrell, Shelton L.
Cornell, Robert F.
Cardiac events during treatment with proteasome inhibitor therapy for multiple myeloma
title Cardiac events during treatment with proteasome inhibitor therapy for multiple myeloma
title_full Cardiac events during treatment with proteasome inhibitor therapy for multiple myeloma
title_fullStr Cardiac events during treatment with proteasome inhibitor therapy for multiple myeloma
title_full_unstemmed Cardiac events during treatment with proteasome inhibitor therapy for multiple myeloma
title_short Cardiac events during treatment with proteasome inhibitor therapy for multiple myeloma
title_sort cardiac events during treatment with proteasome inhibitor therapy for multiple myeloma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048104/
https://www.ncbi.nlm.nih.gov/pubmed/32154000
http://dx.doi.org/10.1186/s40959-017-0023-9
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