Posterior reversible encephalopathy syndrome induced by anti-VEGF agents

106Citations
Citations of this article
58Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Posterior reversible encephalopathy syndrome (PRES) is a clinico-radiological entity that may occur in patients receiving anti-vascular endothelial growth factor (VEGF) agents such as bevacizumab and tyrosine kinase inhibitors. Little is known about the characteristics of patients at risk for PRES under anti-VEGF agents. We carried out a comprehensive review of reports documenting the occurrence of PRES in patients receiving anti-VEGF agents. Twenty-six patients are described with a majority of females (73.1%). Almost a third of patients had a past history of hypertension. The most common symptoms included headache, visual disturbance and seizure. A vast majority of patients had hypertension at the diagnosis of PRES, and proteinuria was detectable each time it was investigated. Neurological outcome was favorable in all cases with a symptomatic treatment including blood pressure control. The risk of PRES is increased when blood pressure is poorly controlled and when proteinuria is detectable. The clinical course appears favorable with a symptomatic treatment. PRES is a potentially severe but manageable toxicity of anti-VEGF agents. © Springer-Verlag 2011.

Cite

CITATION STYLE

APA

Tlemsani, C., Mir, O., Boudou-Rouquette, P., Huillard, O., Maley, K., Ropert, S., … Goldwasser, F. (2011). Posterior reversible encephalopathy syndrome induced by anti-VEGF agents. Targeted Oncology, 6(4), 253–258. https://doi.org/10.1007/s11523-011-0201-x

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free