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Long-term safety and efficacy of add-on cannabidiol in patients with Lennox–Gastaut syndrome: Results of a long-term open-label extension trial

  • Anup D. Patel
  • , Maria Mazurkiewicz-Bełdzińska
  • , Richard F. Chin
  • , Antonio Gil-Nagel
  • , Boudewijn Gunning
  • , Jonathan J. Halford
  • , Wendy Mitchell
  • , Michael Scott Perry
  • , Elizabeth A. Thiele
  • , Arie Weinstock
  • , Eduardo Dunayevich
  • , Daniel Checketts
  • , Orrin Devinsky
  • Nationwide Children’s Hospital
  • Medical University of Gdańsk
  • University of Edinburgh
  • Ruber Internacional Hospital
  • Epilepsy Institutes of the Netherlands Foundation
  • Medical University of South Carolina
  • University of Southern California
  • Cook Children’s Medical Center
  • Massachusetts General Hospital
  • GW Pharmaceuticals
  • New York University

Research output: Contribution to journalArticlepeer-review

107 Scopus citations

Abstract

Objective: Lennox–Gastaut syndrome (LGS) is an epileptic encephalopathy that is often treatment resistant. Efficacy and safety of add-on cannabidiol (CBD) to treat seizures associated with LGS was demonstrated in two randomized controlled trials (RCTs). Patients who completed the RCTs were invited to enroll in this long-term open-label extension (OLE) trial, GWPCARE5 (NCT02224573). We present the final analysis of safety and efficacy outcomes from GWPCARE5. Methods: Patients received plant-derived highly purified CBD (Epidiolex in the United States; Epidyolex in the European Union; 100 mg/ml oral solution), titrated to a target maintenance dose of 20 mg/kg/day over 2 weeks. Based on response and tolerability, CBD could then be reduced or increased up to 30 mg/kg/day. Results: Of 368 patients with LGS who completed the RCTs, 366 (99.5%) enrolled in this OLE. Median and mean treatment duration were 1090 and 826 days (range = 3–1421), respectively, with a mean modal dose of 24 mg/kg/day. Adverse events (AEs) occurred in 96% of patients, serious AEs in 42%, and AE-related discontinuations in 12%. Common AEs were convulsion (39%), diarrhea (38%), pyrexia (34%), and somnolence (29%). Fifty-five (15%) patients experienced liver transaminase elevations more than three times the upper limit of normal; 40 (73%) were taking concomitant valproic acid. Median percent reductions from baseline ranged 48%–71% for drop seizures and 48%–68% for total seizures through 156 weeks. Across all 12-week visit windows, 87% or more of patients/caregivers reported improvement in the patient's overall condition on the Subject/Caregiver Global Impression of Change scale. Significance: Long-term add-on CBD treatment had a similar safety profile as in the original RCTs. Sustained reductions in drop and total seizure frequency were observed for up to 156 weeks, demonstrating long-term benefits of CBD treatment for patients with LGS.

Original languageEnglish
Pages (from-to)2228-2239
Number of pages12
JournalEpilepsia
Volume62
Issue number9
DOIs
StatePublished - Sep 2021

Keywords

  • cannabinoid
  • childhood onset epilepsy
  • drop seizures
  • epileptic encephalopathy
  • treatment resistant

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