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Which is the top player for the cardiovascular safety? ibrutinib vs. obinutuzumab in CLL

Introduction: Ibrutinib, a Bruton’s tyrosine kinase (BTK) inhibitor, is authorized for the treatment of chronic lymphocytic leukemia (CLL). This study aims to explore the cardiac safety profile of ibrutinib in comparison with obinutuzumab. Methods: A retrospective pharmacovigilance study was conduct...

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Autores principales: Mascolo, Annamaria, Di Napoli, Raffaella, Balzano, Nunzia, D’Alessio, Elena, Izzo, Imma, Rossi, Francesco, Paolisso, Giuseppe, Capuano, Annalisa, Sportiello, Liberata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467285/
https://www.ncbi.nlm.nih.gov/pubmed/37654615
http://dx.doi.org/10.3389/fphar.2023.1229304
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author Mascolo, Annamaria
Di Napoli, Raffaella
Balzano, Nunzia
D’Alessio, Elena
Izzo, Imma
Rossi, Francesco
Paolisso, Giuseppe
Capuano, Annalisa
Sportiello, Liberata
author_facet Mascolo, Annamaria
Di Napoli, Raffaella
Balzano, Nunzia
D’Alessio, Elena
Izzo, Imma
Rossi, Francesco
Paolisso, Giuseppe
Capuano, Annalisa
Sportiello, Liberata
author_sort Mascolo, Annamaria
collection PubMed
description Introduction: Ibrutinib, a Bruton’s tyrosine kinase (BTK) inhibitor, is authorized for the treatment of chronic lymphocytic leukemia (CLL). This study aims to explore the cardiac safety profile of ibrutinib in comparison with obinutuzumab. Methods: A retrospective pharmacovigilance study was conducted on data retrieved from the European pharmacovigilance database (Eudravigilance) from 1 January 2014 to 30 September 2022. To compare the reporting frequency of cardiovascular events among ibrutinib, obinutuzumab, and the combination of both. Results: A total of 2 291 CV cases were retrieved, of which 1965 were related to ibrutinib, 312 to obinutuzumab, and 14 to the combination. Most cases referred to patients aged ≥65 years (N = 1,454; 63.47%) and male (N = 1,497; 65.34%). Most cases were serious (N = 2,131; 93.02%). The most reported events were: atrial fibrillation (N = 913; 31.31%) and haemorrhage (N = 201; 6.89%). A higher reporting frequency of CV events was found when ibrutinib was compared to obinutuzumab (ROR, 3.22; 95% CI, 2.89-3.60) or combination (ROR, 1.77; 95% CI, 1.11-2.83). A lower reporting was observed when obinutuzumab was compared to combination (ROR, 0.55; 95% CI, 0.34-0.88). Discussion: A higher reporting frequency of CV events in patients exposed to ibrutinib in comparison with obinutuzumab was found. Further studies are needed to better explore the safety of ibrutinib.
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spelling pubmed-104672852023-08-31 Which is the top player for the cardiovascular safety? ibrutinib vs. obinutuzumab in CLL Mascolo, Annamaria Di Napoli, Raffaella Balzano, Nunzia D’Alessio, Elena Izzo, Imma Rossi, Francesco Paolisso, Giuseppe Capuano, Annalisa Sportiello, Liberata Front Pharmacol Pharmacology Introduction: Ibrutinib, a Bruton’s tyrosine kinase (BTK) inhibitor, is authorized for the treatment of chronic lymphocytic leukemia (CLL). This study aims to explore the cardiac safety profile of ibrutinib in comparison with obinutuzumab. Methods: A retrospective pharmacovigilance study was conducted on data retrieved from the European pharmacovigilance database (Eudravigilance) from 1 January 2014 to 30 September 2022. To compare the reporting frequency of cardiovascular events among ibrutinib, obinutuzumab, and the combination of both. Results: A total of 2 291 CV cases were retrieved, of which 1965 were related to ibrutinib, 312 to obinutuzumab, and 14 to the combination. Most cases referred to patients aged ≥65 years (N = 1,454; 63.47%) and male (N = 1,497; 65.34%). Most cases were serious (N = 2,131; 93.02%). The most reported events were: atrial fibrillation (N = 913; 31.31%) and haemorrhage (N = 201; 6.89%). A higher reporting frequency of CV events was found when ibrutinib was compared to obinutuzumab (ROR, 3.22; 95% CI, 2.89-3.60) or combination (ROR, 1.77; 95% CI, 1.11-2.83). A lower reporting was observed when obinutuzumab was compared to combination (ROR, 0.55; 95% CI, 0.34-0.88). Discussion: A higher reporting frequency of CV events in patients exposed to ibrutinib in comparison with obinutuzumab was found. Further studies are needed to better explore the safety of ibrutinib. Frontiers Media S.A. 2023-08-16 /pmc/articles/PMC10467285/ /pubmed/37654615 http://dx.doi.org/10.3389/fphar.2023.1229304 Text en Copyright © 2023 Mascolo, Di Napoli, Balzano, D’Alessio, Izzo, Rossi, Paolisso, Capuano and Sportiello. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Mascolo, Annamaria
Di Napoli, Raffaella
Balzano, Nunzia
D’Alessio, Elena
Izzo, Imma
Rossi, Francesco
Paolisso, Giuseppe
Capuano, Annalisa
Sportiello, Liberata
Which is the top player for the cardiovascular safety? ibrutinib vs. obinutuzumab in CLL
title Which is the top player for the cardiovascular safety? ibrutinib vs. obinutuzumab in CLL
title_full Which is the top player for the cardiovascular safety? ibrutinib vs. obinutuzumab in CLL
title_fullStr Which is the top player for the cardiovascular safety? ibrutinib vs. obinutuzumab in CLL
title_full_unstemmed Which is the top player for the cardiovascular safety? ibrutinib vs. obinutuzumab in CLL
title_short Which is the top player for the cardiovascular safety? ibrutinib vs. obinutuzumab in CLL
title_sort which is the top player for the cardiovascular safety? ibrutinib vs. obinutuzumab in cll
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467285/
https://www.ncbi.nlm.nih.gov/pubmed/37654615
http://dx.doi.org/10.3389/fphar.2023.1229304
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