Literature DB >> 33681646

Capturing seizures in clinical trials of antiseizure medications for KCNQ2-DEE.

John J Millichap1,2, Cynthia L Harden3, Dennis J Dlugos4, Jacqueline A French5, Noam N Butterfield3, Celene Grayson3, Ernesto Aycardi3, Simon N Pimstone3,6.   

Abstract

Literature review of patients with KCNQ2 developmental and epileptic encephalopathy (KCNQ2-DEE) reveals, based on 16 reports including 139 patients, a clinical phenotype that includes age- and disease-specific stereotyped seizures. The typical seizure type of KCNQ2-DEE, focal tonic, starts within 0-5 days of life and is readily captured by video-electroencephalography VEEG for clinical and genetic diagnosis. After initial identification, KCNQ2-DEE seizures are clinically apparent and can be clearly identified without the use of EEG or VEEG. Therefore, we propose that the 2019 recommendations from the International League against Epilepsy (ILAE), the Pediatric Epilepsy Research Consortium (PERC), for capturing and recording seizures for clinical trials (Epilepsia Open, 4, 2019, 537) are suitable for use in KCNQ2-DEE‒associated antiseizure medicine (ASM) treatment trials. The ILAE/PERC consensus guidance states that a caregiver-maintained seizure diary, completed by caregivers who are trained to recognize seizures using within-patient historical recordings, accurately captures seizures prospectively in a clinical trial. An alternative approach historically endorsed by the Food and Drug Administration (FDA) compares seizure counts captured on VEEG before and after treatment. A major advantage of the ILAE/PERC strategy is that it expands the numbers of eligible patients who meet inclusion criteria of clinical trials while maintaining accurate seizure counts (Epilepsia Open, 4, 2019, 537). Three recent phase 3 pivotal pediatric trials investigating ASMs to treat syndromic seizures in patients as young as 2 years of age (N Engl J Med, 17, 2017, 699; Lancet, 21, 2020, 2243; Lancet, 17, 2018, 1085); and ongoing phase 2 open-label pediatric clinical trial that includes pediatric epileptic syndromes as young as 1 month of age (Am J Med Genet A, 176, 2018, 773), have already used caregiver-maintained seizure diaries successfully. For determining the outcome of a KCNQ2-DEE ASM treatment trial, the use of a seizure diary to count seizures by trained observers is feasible because the seizures of KCNQ2-DEE are clinically apparent. This strategy is supported by successful precedent in clinical trials in similar age groups and has the endorsement of the international pediatric epilepsy community.
© 2021 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.

Entities:  

Keywords:  KCNQ2; epilepsy; seizure diaries; tonic seizures; video‐EEG

Mesh:

Substances:

Year:  2021        PMID: 33681646      PMCID: PMC7918316          DOI: 10.1002/epi4.12466

Source DB:  PubMed          Journal:  Epilepsia Open        ISSN: 2470-9239


  26 in total

1.  KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.

Authors:  Sarah Weckhuysen; Simone Mandelstam; Arvid Suls; Dominique Audenaert; Tine Deconinck; Lieve R F Claes; Liesbet Deprez; Katrien Smets; Dimitrina Hristova; Iglika Yordanova; Albena Jordanova; Berten Ceulemans; An Jansen; Danièle Hasaerts; Filip Roelens; Lieven Lagae; Simone Yendle; Thorsten Stanley; Sarah E Heron; John C Mulley; Samuel F Berkovic; Ingrid E Scheffer; Peter de Jonghe
Journal:  Ann Neurol       Date:  2012-01       Impact factor: 10.422

2.  Oxcarbazepine adjunctive therapy in infants and young children with partial seizures.

Authors:  J E Piña-Garza; R Espinoza; D Nordli; D A Bennett; S Spirito; T E Stites; D Tang; Y Sturm
Journal:  Neurology       Date:  2005-11-08       Impact factor: 9.910

3.  Sodium channel blockers in KCNQ2-encephalopathy: Lacosamide as a new treatment option.

Authors:  Susanne Schubert-Bast; Peter Hofstetter; Doris Fischer; Rolf Schloesser; Georgia Ramantani; Matthias Kieslich
Journal:  Seizure       Date:  2017-09-01       Impact factor: 3.184

4.  Genetics and genotype-phenotype correlations in early onset epileptic encephalopathy with burst suppression.

Authors:  Heather E Olson; McKenna Kelly; Christopher M LaCoursiere; Rebecca Pinsky; Dimira Tambunan; Catherine Shain; Sriram Ramgopal; Masanori Takeoka; Mark H Libenson; Kristina Julich; Tobias Loddenkemper; Eric D Marsh; Devorah Segal; Susan Koh; Michael S Salman; Alex R Paciorkowski; Edward Yang; Ann M Bergin; Beth Rosen Sheidley; Annapurna Poduri
Journal:  Ann Neurol       Date:  2017-02-14       Impact factor: 10.422

5.  Cannabidiol in patients with seizures associated with Lennox-Gastaut syndrome (GWPCARE4): a randomised, double-blind, placebo-controlled phase 3 trial.

Authors:  Elizabeth A Thiele; Eric D Marsh; Jacqueline A French; Maria Mazurkiewicz-Beldzinska; Selim R Benbadis; Charuta Joshi; Paul D Lyons; Adam Taylor; Claire Roberts; Kenneth Sommerville
Journal:  Lancet       Date:  2018-01-26       Impact factor: 79.321

6.  Adjunctive lamotrigine for partial seizures in patients aged 1 to 24 months.

Authors:  J E Piña-Garza; P Levisohn; K Gucuyener; M A Mikati; C R Warnock; H S Conklin; J Messenheimer
Journal:  Neurology       Date:  2007-12-12       Impact factor: 9.910

7.  Targeted gene panel and genotype-phenotype correlation in children with developmental and epileptic encephalopathy.

Authors:  Ara Ko; Song Ee Youn; Se Hee Kim; Joon Soo Lee; Sangwoo Kim; Jong Rak Choi; Heung Dong Kim; Seung-Tae Lee; Hoon-Chul Kang
Journal:  Epilepsy Res       Date:  2018-02-12       Impact factor: 3.045

8.  Adjunctive levetiracetam in infants and young children with refractory partial-onset seizures.

Authors:  Jesus Eric Piña-Garza; Douglas R Nordli; Dietz Rating; Haichen Yang; Jimmy Schiemann-Delgado; Benjamin Duncan
Journal:  Epilepsia       Date:  2009-02-21       Impact factor: 5.864

9.  Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial.

Authors:  Lieven Lagae; Joseph Sullivan; Kelly Knupp; Linda Laux; Tilman Polster; Marina Nikanorova; Orrin Devinsky; J Helen Cross; Renzo Guerrini; Dinesh Talwar; Ian Miller; Gail Farfel; Bradley S Galer; Arnold Gammaitoni; Arun Mistry; Glenn Morrison; Michael Lock; Anupam Agarwal; Wyman W Lai; Berten Ceulemans
Journal:  Lancet       Date:  2019-12-17       Impact factor: 79.321

10.  KCNQ2 encephalopathy: Features, mutational hot spots, and ezogabine treatment of 11 patients.

Authors:  John J Millichap; Kristen L Park; Tammy Tsuchida; Bruria Ben-Zeev; Lionel Carmant; Robert Flamini; Nishtha Joshi; Paul M Levisohn; Eric Marsh; Srishti Nangia; Vinodh Narayanan; Xilma R Ortiz-Gonzalez; Marc C Patterson; Phillip L Pearl; Brenda Porter; Keri Ramsey; Emily L McGinnis; Maurizio Taglialatela; Molly Tracy; Baouyen Tran; Charu Venkatesan; Sarah Weckhuysen; Edward C Cooper
Journal:  Neurol Genet       Date:  2016-08-22
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.