2020
DOI: 10.1002/ejhf.1847
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Cardiotoxicity and myocardial hypoperfusion associated with anti‐vascular endothelial growth factor therapies: prospective cardiac magnetic resonance imaging in patients with cancer

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Cited by 14 publications
(18 citation statements)
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“…385 HF can develop as a consequence of the toxic effects of anti-cancer therapy (cardiotoxicity). 383,[386][387][388] In patients treated with immune checkpoint inhibitors (ICIs), pharmacovigilance data analysis reported an incidence of 4.2% of cardiac events, including myocarditis, which was often burdened by a high mortality. 389,390 The incidence of cardiac events was higher in those patients with dual ICI therapy.…”
Section: Cancer Treatmentmentioning
confidence: 99%
“…385 HF can develop as a consequence of the toxic effects of anti-cancer therapy (cardiotoxicity). 383,[386][387][388] In patients treated with immune checkpoint inhibitors (ICIs), pharmacovigilance data analysis reported an incidence of 4.2% of cardiac events, including myocarditis, which was often burdened by a high mortality. 389,390 The incidence of cardiac events was higher in those patients with dual ICI therapy.…”
Section: Cancer Treatmentmentioning
confidence: 99%
“…Cancer is a risk factor for HF 20–23 . In a prospective cohort study of 146 817 post‐menopausal women, Leedy et al 24 .…”
Section: Comorbiditiesmentioning
confidence: 99%
“…Cancer is a risk factor for HF. [20][21][22][23] In a prospective cohort study of 146 817 post-menopausal women, Leedy et al 24 showed that HF was associated with an increased risk of subsequent cancer [hazard ratio (HR) 1.28, 95% confidence interval (CI) 1.11-1.48], namely obesity-related, lung and colorectal cancers. In patients treated with immune checkpoint inhibitors (ICIs), pharmacovigilance data analysis reported an incidence of 4.2% of cardiac events, including myocarditis, which was often burdened by a high mortality.…”
Section: Cardio-oncologymentioning
confidence: 99%
“…The resulting myocardial hypoxia leads to sustained expression of hypoxia-inducible factor alpha (HIF-), which was demonstrated to be sufficient to cause cardiomyopathy 36 , 37 . Indeed, enhanced vascular permeability and reversible microvascular vasoconstriction have been reported in patients receiving therapies targeting VEGF and PDGF receptor (VEGFR and PDGFR, respectively) 38 . Moreover, this mechanism of toxicity well explains the clinical observation that cardiomyopathy associated with anti-VEGFR/PDGFR agents is reversible 39 .…”
Section: Role Of Non-cardiomyocytes In Cancer Treatment-related Cardiotoxicitymentioning
confidence: 99%