Evaluation of cardiovascular toxicity of the atezolizumab and bevacizumab combination

Introduction: The combination of atezolizumab, an immune checkpoint inhibitor (ICI), and bevacizumab, a vascular endothelial growth factor (VEGF) inhibitor, is the first choice for systemic therapy in hepatocellular carcinoma. Immune-related cardiovascular toxicity-myocarditis and pericarditis-are k...

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Main Authors: Takahiro Niimura (Author), Mitsuhiro Goda (Author), Koji Miyata (Author), Jun Matsumoto (Author), Toshihiko Yoshioka (Author), Hirofumi Hamano (Author), Fuka Aizawa (Author), Kenta Yagi (Author), Yuki Izawa-Ishizawa (Author), Yoshito Zamami (Author), Keisuke Ishizawa (Author)
Format: Book
Published: Frontiers Media S.A., 2023-08-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Takahiro Niimura  |e author 
700 1 0 |a Takahiro Niimura  |e author 
700 1 0 |a Mitsuhiro Goda  |e author 
700 1 0 |a Mitsuhiro Goda  |e author 
700 1 0 |a Koji Miyata  |e author 
700 1 0 |a Jun Matsumoto  |e author 
700 1 0 |a Toshihiko Yoshioka  |e author 
700 1 0 |a Toshihiko Yoshioka  |e author 
700 1 0 |a Hirofumi Hamano  |e author 
700 1 0 |a Hirofumi Hamano  |e author 
700 1 0 |a Fuka Aizawa  |e author 
700 1 0 |a Fuka Aizawa  |e author 
700 1 0 |a Kenta Yagi  |e author 
700 1 0 |a Kenta Yagi  |e author 
700 1 0 |a Yuki Izawa-Ishizawa  |e author 
700 1 0 |a Yuki Izawa-Ishizawa  |e author 
700 1 0 |a Yoshito Zamami  |e author 
700 1 0 |a Yoshito Zamami  |e author 
700 1 0 |a Keisuke Ishizawa  |e author 
700 1 0 |a Keisuke Ishizawa  |e author 
700 1 0 |a Keisuke Ishizawa  |e author 
245 0 0 |a Evaluation of cardiovascular toxicity of the atezolizumab and bevacizumab combination 
260 |b Frontiers Media S.A.,   |c 2023-08-01T00:00:00Z. 
500 |a 2674-0869 
500 |a 10.3389/fdsfr.2023.1213771 
520 |a Introduction: The combination of atezolizumab, an immune checkpoint inhibitor (ICI), and bevacizumab, a vascular endothelial growth factor (VEGF) inhibitor, is the first choice for systemic therapy in hepatocellular carcinoma. Immune-related cardiovascular toxicity-myocarditis and pericarditis-are known to occur during ICI treatment. By contrast, VEGF inhibitors (VEGFIs) cause cardiovascular complications such as hypertension and heart failure. Thus, different cardiovascular toxicities have been recognized for ICIs and VEGFIs, but the impact of their combination remains unclear. Here, we aimed to investigate the cardiovascular toxicity profile of atezolizumab in combination with bevacizumab using the World Health Organization adverse event reporting database-VigiBase.Methods: We analyzed data included in VigiBase till December 2022. To evaluate the frequency of reports related to atezolizumab, bevacizumab, and their combinations for 21 adverse events, we calculated the reporting odds ratio and information component. Analyses of the fatality of various cardiovascular toxicities associated with the use of each drug were performed.Results: The database included 84,951, 10,595, and 2,092 reports of treatment with bevacizumab, atezolizumab, and their combination, respectively. The disproportionality signal of hypertension, arterial embolism and thrombosis, supraventricular tachyarrhythmias, heart failure, myocarditis, hemorrhage-related clinical events, venous embolism and thrombosis, cardiomyopathy, respiratory failure with combination regimen of atezolizumab and bevacizumab was detected. Signals of these adverse events were also detected treatment with either atezolizumab or bevacizumab alone. Venous embolism and thrombosis exhibited the highest fatality rate in the two drug combination (12.82%) relative to those of atezolizumab (6.19%) and bevacizumab (4.54%).Discussion: Cardiovascular toxicity, owing to the combination of atezolizumab and bevacizumab, was similar to that of each single agent, and no new safety concerns were observed. Caution should be exercised when combining the two drugs since the fatality rate of thromboembolism increases with combination treatment. 
546 |a EN 
690 |a atezolizumab 
690 |a bevacizumab 
690 |a cardiovascular toxicity 
690 |a thromboembolism 
690 |a adverse event 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Frontiers in Drug Safety and Regulation, Vol 3 (2023) 
787 0 |n https://www.frontiersin.org/articles/10.3389/fdsfr.2023.1213771/full 
787 0 |n https://doaj.org/toc/2674-0869 
856 4 1 |u https://doaj.org/article/8a1d42f6d3384d1e8455f73b217efc07  |z Connect to this object online.