TY - JOUR
T1 - Long-term safety and treatment effects of cannabidiol in children and adults with treatment-resistant epilepsies
T2 - Expanded access program results
AU - CBD EAP study group
AU - Szaflarski, Jerzy P.
AU - Bebin, Elizabeth Martina
AU - Comi, Anne M.
AU - Patel, Anup D.
AU - Joshi, Charuta
AU - Checketts, Daniel
AU - Beal, Jules C.
AU - Laux, Linda C.
AU - De Boer, Lisa M.
AU - Wong, Matthew H.
AU - Lopez, Merrick
AU - Devinsky, Orrin
AU - Lyons, Paul D.
AU - Zentil, Pilar Pichon
AU - Wechsler, Robert
AU - Chez, Michael
AU - Flamini, Robert
AU - Marsh, Eric D.
AU - Miller, Ian
AU - Park, Yong
AU - Segal, Eric
AU - Seltzer, Laurie
AU - Thiele, Elizabeth A.
AU - Weinstock, Arie
N1 - Publisher Copyright:
© 2018 The Authors. Epilepsia published by Wiley Periodicals, Inc. on behalf of International League Against Epilepsy.
PY - 2018/8
Y1 - 2018/8
N2 - Objective: Since 2014, cannabidiol (CBD) has been administered to patients with treatment-resistant epilepsies (TREs) in an ongoing expanded-access program (EAP). We report interim results on the safety and efficacy of CBD in EAP patients treated through December 2016. Methods: Twenty-five US-based EAP sites enrolling patients with TRE taking stable doses of antiepileptic drugs (AEDs) at baseline were included. During the 4-week baseline period, parents/caregivers kept diaries of all countable seizure types. Patients received oral CBD starting at 2-10 mg/kg/d, titrated to a maximum dose of 25-50 mg/kg/d. Patient visits were every 2-4 weeks through 16 weeks and every 2-12 weeks thereafter. Efficacy endpoints included the percentage change from baseline in median monthly convulsive and total seizure frequency, and percentage of patients with ≥50%, ≥75%, and 100% reductions in seizures vs baseline. Data were analyzed descriptively for the efficacy analysis set and using the last-observation-carried-forward method to account for missing data. Adverse events (AEs) were documented at each visit. Results: Of 607 patients in the safety dataset, 146 (24%) withdrew; the most common reasons were lack of efficacy (89 [15%]) and AEs (32 [5%]). Mean age was 13 years (range, 0.4-62). Median number of concomitant AEDs was 3 (range, 0-10). Median CBD dose was 25 mg/kg/d; median treatment duration was 48 weeks. Add-on CBD reduced median monthly convulsive seizures by 51% and total seizures by 48% at 12 weeks; reductions were similar through 96 weeks. Proportion of patients with ≥50%, ≥75%, and 100% reductions in convulsive seizures were 52%, 31%, and 11%, respectively, at 12 weeks, with similar rates through 96 weeks. CBD was generally well tolerated; most common AEs were diarrhea (29%) and somnolence (22%). Significance: Results from this ongoing EAP support previous observational and clinical trial data showing that add-on CBD may be an efficacious long-term treatment option for TRE.
AB - Objective: Since 2014, cannabidiol (CBD) has been administered to patients with treatment-resistant epilepsies (TREs) in an ongoing expanded-access program (EAP). We report interim results on the safety and efficacy of CBD in EAP patients treated through December 2016. Methods: Twenty-five US-based EAP sites enrolling patients with TRE taking stable doses of antiepileptic drugs (AEDs) at baseline were included. During the 4-week baseline period, parents/caregivers kept diaries of all countable seizure types. Patients received oral CBD starting at 2-10 mg/kg/d, titrated to a maximum dose of 25-50 mg/kg/d. Patient visits were every 2-4 weeks through 16 weeks and every 2-12 weeks thereafter. Efficacy endpoints included the percentage change from baseline in median monthly convulsive and total seizure frequency, and percentage of patients with ≥50%, ≥75%, and 100% reductions in seizures vs baseline. Data were analyzed descriptively for the efficacy analysis set and using the last-observation-carried-forward method to account for missing data. Adverse events (AEs) were documented at each visit. Results: Of 607 patients in the safety dataset, 146 (24%) withdrew; the most common reasons were lack of efficacy (89 [15%]) and AEs (32 [5%]). Mean age was 13 years (range, 0.4-62). Median number of concomitant AEDs was 3 (range, 0-10). Median CBD dose was 25 mg/kg/d; median treatment duration was 48 weeks. Add-on CBD reduced median monthly convulsive seizures by 51% and total seizures by 48% at 12 weeks; reductions were similar through 96 weeks. Proportion of patients with ≥50%, ≥75%, and 100% reductions in convulsive seizures were 52%, 31%, and 11%, respectively, at 12 weeks, with similar rates through 96 weeks. CBD was generally well tolerated; most common AEs were diarrhea (29%) and somnolence (22%). Significance: Results from this ongoing EAP support previous observational and clinical trial data showing that add-on CBD may be an efficacious long-term treatment option for TRE.
KW - cannabidiol
KW - efficacy
KW - expanded access program
KW - seizures
KW - tolerability
KW - treatment-resistant epilepsy
KW - United States
KW - Humans
KW - Middle Aged
KW - Child, Preschool
KW - Infant
KW - Male
KW - Treatment Outcome
KW - Anticonvulsants/therapeutic use
KW - Dose-Response Relationship, Drug
KW - Young Adult
KW - Adolescent
KW - Cannabidiol/therapeutic use
KW - Adult
KW - Drug Resistant Epilepsy/drug therapy
KW - Female
KW - Child
KW - Longitudinal Studies
KW - Infant, Newborn
UR - https://www.scopus.com/pages/publications/85050490233
UR - https://www.scopus.com/pages/publications/85050490233#tab=citedBy
UR - https://www.mendeley.com/catalogue/592a7ffe-2d3c-3416-8d8c-54e6e7b583c3/
U2 - 10.1111/epi.14477
DO - 10.1111/epi.14477
M3 - Article
C2 - 29998598
SN - 0013-9580
VL - 59
SP - 1540
EP - 1548
JO - Epilepsia
JF - Epilepsia
IS - 8
ER -