Long‐term effectiveness of add‐on perampanel in patients with Lennox–Gastaut syndrome: A multicenter retrospective study

This retrospective study assessed long‐term effectiveness of add‐on perampanel (PER) in patients with Lennox–Gastaut syndrome (LGS). Outcomes included time to PER failure and time to seizure relapse in responders. PER failure was defined as either discontinuation of PER or initiation of another trea...

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Published inEpilepsia (Copenhagen) Vol. 64; no. 6; pp. e98 - e104
Main Authors Matricardi, Sara, Cesaroni, Elisabetta, Bonanni, Paolo, Foschi, Nicoletta, D′Aniello, Alfredo, Di Gennaro, Giancarlo, Striano, Pasquale, Cappanera, Silvia, Siliquini, Sabrina, Freri, Elena, Ragona, Francesca, Granata, Tiziana, Deleo, Francesco, Villani, Flavio, Russo, Angelo, Messana, Tullio, Siri, Laura, Bagnasco, Irene, Vignoli, Aglaia, Operto, Francesca Felicia, Orsini, Alessandro, Bonuccelli, Alice, Papa, Amanda, Peruzzi, Cinzia, Liguori, Claudio, Verrotti, Alberto, Chiarelli, Francesco, Marini, Carla, Lattanzi, Simona
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Abstract This retrospective study assessed long‐term effectiveness of add‐on perampanel (PER) in patients with Lennox–Gastaut syndrome (LGS). Outcomes included time to PER failure and time to seizure relapse in responders. PER failure was defined as either discontinuation of PER or initiation of another treatment. Seizure relapse in responders was defined as occurrence of a seizure in seizure‐free patients and increase of at least 50% in average monthly seizure frequency for those who were responders. Eighty‐seven patients were included. Treatment failure occurred in 52 (59.8%) subjects at a median time of 12 months. Treatment failure was due to lack of efficacy in 27 (52.0%) patients, lack of tolerability in 14 (27.0%), and both reasons in 11 (21.0%). A slower titration was associated with a lower risk of PER failure compared to faster titration schedules, and the occurrence of adverse events increased the risk of treatment failure. Thirty‐six patients (41.4%) were responders during a median follow‐up of 11 months. Seizure relapse occurred in 13 of 36 (36.1%) patients after a median time of 21 months. The overall rate of seizure responders was 23 of 87 (26.4%) at the end of follow‐up. This study provides real‐world evidence on the effectiveness of PER as adjunctive treatment in LGS patients.
AbstractList This retrospective study assessed long-term effectiveness of add-on perampanel (PER) in patients with Lennox-Gastaut syndrome (LGS). Outcomes included time to PER failure and time to seizure relapse in responders. PER failure was defined as either discontinuation of PER or initiation of another treatment. Seizure relapse in responders was defined as occurrence of a seizure in seizure-free patients and increase of at least 50% in average monthly seizure frequency for those who were responders. Eighty-seven patients were included. Treatment failure occurred in 52 (59.8%) subjects at a median time of 12 months. Treatment failure was due to lack of efficacy in 27 (52.0%) patients, lack of tolerability in 14 (27.0%), and both reasons in 11 (21.0%). A slower titration was associated with a lower risk of PER failure compared to faster titration schedules, and the occurrence of adverse events increased the risk of treatment failure. Thirty-six patients (41.4%) were responders during a median follow-up of 11 months. Seizure relapse occurred in 13 of 36 (36.1%) patients after a median time of 21 months. The overall rate of seizure responders was 23 of 87 (26.4%) at the end of follow-up. This study provides real-world evidence on the effectiveness of PER as adjunctive treatment in LGS patients.
This retrospective study assessed long-term effectiveness of add-on perampanel (PER) in patients with Lennox-Gastaut syndrome (LGS). Outcomes included time to PER failure and time to seizure relapse in responders. PER failure was defined as either discontinuation of PER or initiation of another treatment. Seizure relapse in responders was defined as occurrence of a seizure in seizure-free patients and increase of at least 50% in average monthly seizure frequency for those who were responders. Eighty-seven patients were included. Treatment failure occurred in 52 (59.8%) subjects at a median time of 12 months. Treatment failure was due to lack of efficacy in 27 (52.0%) patients, lack of tolerability in 14 (27.0%), and both reasons in 11 (21.0%). A slower titration was associated with a lower risk of PER failure compared to faster titration schedules, and the occurrence of adverse events increased the risk of treatment failure. Thirty-six patients (41.4%) were responders during a median follow-up of 11 months. Seizure relapse occurred in 13 of 36 (36.1%) patients after a median time of 21 months. The overall rate of seizure responders was 23 of 87 (26.4%) at the end of follow-up. This study provides real-world evidence on the effectiveness of PER as adjunctive treatment in LGS patients.This retrospective study assessed long-term effectiveness of add-on perampanel (PER) in patients with Lennox-Gastaut syndrome (LGS). Outcomes included time to PER failure and time to seizure relapse in responders. PER failure was defined as either discontinuation of PER or initiation of another treatment. Seizure relapse in responders was defined as occurrence of a seizure in seizure-free patients and increase of at least 50% in average monthly seizure frequency for those who were responders. Eighty-seven patients were included. Treatment failure occurred in 52 (59.8%) subjects at a median time of 12 months. Treatment failure was due to lack of efficacy in 27 (52.0%) patients, lack of tolerability in 14 (27.0%), and both reasons in 11 (21.0%). A slower titration was associated with a lower risk of PER failure compared to faster titration schedules, and the occurrence of adverse events increased the risk of treatment failure. Thirty-six patients (41.4%) were responders during a median follow-up of 11 months. Seizure relapse occurred in 13 of 36 (36.1%) patients after a median time of 21 months. The overall rate of seizure responders was 23 of 87 (26.4%) at the end of follow-up. This study provides real-world evidence on the effectiveness of PER as adjunctive treatment in LGS patients.
Author Verrotti, Alberto
Bonuccelli, Alice
Matricardi, Sara
Siri, Laura
Granata, Tiziana
Vignoli, Aglaia
Operto, Francesca Felicia
Ragona, Francesca
Foschi, Nicoletta
Bagnasco, Irene
Peruzzi, Cinzia
Chiarelli, Francesco
Russo, Angelo
Striano, Pasquale
Papa, Amanda
D′Aniello, Alfredo
Cappanera, Silvia
Villani, Flavio
Orsini, Alessandro
Freri, Elena
Bonanni, Paolo
Siliquini, Sabrina
Cesaroni, Elisabetta
Di Gennaro, Giancarlo
Marini, Carla
Messana, Tullio
Liguori, Claudio
Deleo, Francesco
Lattanzi, Simona
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Copyright 2023 The Authors. published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.
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– notice: 2023. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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Issue 6
Keywords perampanel
LGS
Lennox-Gastaut syndrome
developmental and epileptic encephalopathy
real-world evidence
Language English
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Snippet This retrospective study assessed long‐term effectiveness of add‐on perampanel (PER) in patients with Lennox–Gastaut syndrome (LGS). Outcomes included time to...
This retrospective study assessed long-term effectiveness of add-on perampanel (PER) in patients with Lennox-Gastaut syndrome (LGS). Outcomes included time to...
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SubjectTerms Anticonvulsants - therapeutic use
developmental and epileptic encephalopathy
Humans
Lennox Gastaut Syndrome - drug therapy
Lennox–Gastaut syndrome
LGS
perampanel
real‐world evidence
Retrospective Studies
Seizures
Seizures - drug therapy
Titration
Treatment Outcome
Title Long‐term effectiveness of add‐on perampanel in patients with Lennox–Gastaut syndrome: A multicenter retrospective study
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fepi.17601
https://www.ncbi.nlm.nih.gov/pubmed/37000415
https://www.proquest.com/docview/2821504801
https://www.proquest.com/docview/2793989861
Volume 64
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