Treatment with Cenobamate in Adult Patients with Lennox-Gastaut Syndrome: A Case Series

被引:22
作者
Falcicchio, Giovanni [1 ]
Lattanzi, Simona [2 ]
Negri, Francesco [1 ]
de Tommaso, Marina [1 ]
La Neve, Angela [1 ]
Specchio, Nicola [3 ]
机构
[1] Univ Barialdo Moro, DiBraiN Dept, I-70124 Bari, Italy
[2] Marche Polytech Univ, Dept Expt & Clin Med, Neurol Clin, I-60020 Ancona, Italy
[3] Bambino Gesu Pediat Hosp, IRCCS, I-00146 Rome, Italy
关键词
epilepsy; cenobamate; Lennox-Gastaut syndrome; epileptic encephalopathy; drug-resistant epilepsy; DEFINITION;
D O I
10.3390/jcm12010129
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Lennox-Gastaut syndrome (LGS) is a developmental and epileptic encephalopathy (DEE) in which drug resistance to antiepileptic drugs (AEDs) is common. Focal-onset seizures (FOS) are among the seizure types characterizing LGS. Cenobamate (CNB) is a new AED indicated for the treatment of FOS and it has shown promising results in terms of seizure frequency reduction in both clinical trials and real-world experience. To date, the use of CNB in patients with DEEs is limited to Dravet syndrome. Methods: This was a retrospective study aimed to determine the 12-month effectiveness and tolerability of CNB in patients with LGS following real-world practice. Results: Four patients with LGS receiving CNB treatment were identified. At 12 months from starting CNB, the reduction in baseline seizure frequency ranged from 25 to 74%, with two patients achieving >= 50% seizure reduction. CNB was generally well tolerated and adjustments in doses of concomitant AEDs were required. Conclusions: CNB may represent a promising therapeutic option in patients with drug-resistant epilepsy associated with LGS. Further research is needed to confirm this preliminary evidence.
引用
收藏
页数:7
相关论文
共 20 条
[1]  
[Anonymous], About us
[2]   Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology [J].
Arzimanoglou, Alexis ;
French, Jacqueline ;
Blume, Warren T. ;
Cross, J. Helen ;
Ernst, Jan-Peter ;
Feucht, Martha ;
Genton, Pierre ;
Guerrini, Renzo ;
Kluger, Gerhard ;
Pellock, John M. ;
Perucca, Emilio ;
Wheless, James W. .
LANCET NEUROLOGY, 2009, 8 (01) :82-93
[3]   Cluster analysis of a large dataset of patients with Lennox-Gastaut syndrome [J].
Asadi-Pooya, Ali A. ;
Bazrafshan, Mehdi ;
Farazdaghi, Mohsen .
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2021, 92 :36-39
[4]   Lennox-Gastaut syndrome: a comprehensive review [J].
Asadi-Pooya, Ali A. .
NEUROLOGICAL SCIENCES, 2018, 39 (03) :403-414
[5]   Lennox-Gastaut syndrome in south Iran: Electro-clinical manifestations [J].
Asadi-Pooya, Ali A. ;
Sharifzade, Mohaddese .
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2012, 21 (10) :760-763
[6]   Drug Development for Rare Paediatric Epilepsies: Current State and Future Directions [J].
Auvin, Stephane ;
Avbersek, Andreja ;
Bast, Thomas ;
Chiron, Catherine ;
Guerrini, Renzo ;
Kaminski, Rafal M. ;
Lagae, Lieven ;
Muglia, Pierandrea ;
Cross, J. Helen .
DRUGS, 2019, 79 (18) :1917-1935
[7]   Definition and natural history of Lennox-Gastaut syndrome [J].
Camfield, Peter R. .
EPILEPSIA, 2011, 52 :3-9
[8]   Effectiveness and safety of adjunctive cenobamate for focal seizures in adults with developmental disability treated in clinical practice [J].
Connor, Gregory S. ;
Williamson, Amanda .
EPILEPSY & BEHAVIOR REPORTS, 2022, 18
[9]   Expert Opinion on the Management of Lennox-Gastaut Syndrome: Treatment Algorithms and Practical Consideration [J].
Cross, J. Helen ;
Auvin, Stephane ;
Falip, Merce ;
Striano, Pasquale ;
Arzimanoglou, Alexis .
FRONTIERS IN NEUROLOGY, 2017, 8
[10]   Seizure diaries for clinical research and practice: Limitations and future prospects [J].
Fisher, Robert S. ;
Blum, David E. ;
DiVentura, Bree ;
Vannest, Jennifer ;
Hixson, John D. ;
Moss, Robert ;
Herman, Susan T. ;
Fureman, Brandy E. ;
French, Jacqueline A. .
EPILEPSY & BEHAVIOR, 2012, 24 (03) :304-310