Perampanel in Brain Tumor-Related Epilepsy: A Systematic Review

被引:16
作者
Damavandi, Payam Tabaee [1 ]
Pasini, Francesco [1 ]
Fanella, Gaia [1 ]
Cereda, Giulia Sofia [1 ]
Mainini, Gabriele [1 ]
DiFrancesco, Jacopo C. [1 ]
Trinka, Eugen [2 ,3 ,4 ]
Lattanzi, Simona [5 ]
机构
[1] Univ Milano Bicocca, Fdn IRCCS San Gerardo Tintori, Milan Ctr Neurosci, Sch Med & Surg,Dept Neurol, I-20900 Monza, Italy
[2] Paracelsus Med Univ, Dept Neurol, Christian Doppler Klin, A-5020 Salzburg, Austria
[3] Ctr Cognit Neurosci, A-5020 Salzburg, Austria
[4] Univ Hlth Sci Med Informat & Technol, Publ Hlth Hlth Serv Res HTA, A-6060 Hall In Tirol, Austria
[5] Marche Polytech Univ, Dept Expt & Clin Med, Neurol Clin, I-60020 Ancona, Italy
基金
奥地利科学基金会;
关键词
perampanel; AMPA receptors; brain tumor; epilepsy; glutamate; glioma; seizure; glioblastoma; GLIOBLASTOMA-MULTIFORME; GLUTAMATE; SEIZURES; PROLIFERATION; TEMOZOLOMIDE; CONCOMITANT; TALAMPANEL; SURVIVAL; GROWTH; IMPACT;
D O I
10.3390/brainsci13020326
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Brain tumor-related epilepsy (BTRE) is a common comorbidity in patients with brain neoplasms and it may be either the first symptom or develop after the tumor diagnosis. Increasing evidence suggests that brain tumors and BTRE share common pathophysiological mechanisms. Glutamatergic mechanisms can play a central role in promoting both primary brain tumor growth and epileptogenesis. Perampanel (PER), which acts as a selective antagonist of glutamate alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, may play a role both in the reduction in tumor growth and the control of epileptiform activity. This systematic review aimed to summarize the pre-clinical and clinical evidence about the antitumor properties, antiseizure effects and tolerability of PER in BTRE. Eight pre-clinical and eight clinical studies were identified. The currently available evidence suggests that PER can be an effective and generally well-tolerated therapeutic option in patients with BTRE. In vitro studies demonstrated promising antitumor activity of PER, while no role in slowing tumor progression has been demonstrated in rat models; clinical data on the potential antitumor activity of PER are scarce. Additional studies are needed to explore further the effects of PER on tumor progression and fully characterize its potentialities in patients with BTRE.
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页数:13
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