Study register · detail
Clear benefit
GRADE
High
44 citations
Samplen = 132 Pat.
Duration12, 24 and 48 weeks
ControlInternal comparison groups
EndpointSeizure frequency
Blindingoffen
DesignProspektive Open-Label-Studie (Expanded Access Program)
Cannabinoidcbd
Routeoral
Key finding
CBD significantly reduces seizure frequency and severity, without drug interactions with co-medications influencing treatment response.
Summary
n=132 adults and children with treatment-resistant epilepsy (TRE) on CBD (Epidiolex®) with/without clobazam co-medication. All groups showed significant reductions in seizure frequency and severity compared to baseline (all p<0,05). No significant difference in treatment response between CBD+clobazam vs. CBD-clobazam at 12 weeks (both p>0,05). No influence of other interacting AEDs on treatment success up to 48 weeks (all p>0,05).
P
PopulationAdults and children with treatment-resistant epilepsy (TRE), n=132
I
InterventionCannabidiol (CBD; Epidiolex®) as add-on therapy to existing antiepileptic drugs (with or without clobazam)
C
ControlInternal comparison groups: CBD + clobazam vs. CBD without clobazam; as well as groups with vs. without interacting antiepileptic drugs
O
OutcomeAll groups showed significant reductions in seizure frequency and severity from baseline (p<0,05); no significant group differences at any time point (12, 24, 48 weeks, all p>0,05)
Confidence in the evidence
High
The highest of four GRADE levels, the effect estimate is very reliable.
Quality profile
Sample size
★★★★★
Blinding
Open-label
Effect size
Clear benefit
Citations / year
★★★★★
Authors
Share
Abstract
<h4>Objective</h4>We have previously shown that cannabidiol (CBD; Epidiolex®) significantly affects levels of clobazam/N-desmethylclobazam, rufinamide, topiramate, zonisamide, and eslicarbazepine. In the present study, we tested whether the presence of concomitant clobazam affected seizure frequency and severity (treatment response) 12 weeks after initiation of therapy with CBD in patients with treatment-resistant epilepsy (TRE). The secondary questions were whether the presence of any of the other antiepileptic drugs (AEDs) had an effect on seizure frequency or severity at 12, 24, or 48 weeks after therapy initiation.<h4>Methods</h4>One hundred and thirty-two adults and children with TRE receiving CBD were studied prospectively. Participants were separated into two groups - either taking (CBD + clobazam) or not taking concomitant clobazam (CBD - clobazam). In the secondary analyses, participants were divided into groups depending on whether they were taking at least 1/4 of the other AEDs shown to interact with CBD (iAED). Seizure counts and Chalfont Seizure Severity Scale (CSSS) were obtained at baseline, 12, 24, and 48 weeks. Groups were compared at each respective time point in the study using generalized estimating equations (GEE) analyses.<h4>Results</h4>All groups demonstrated statistically significant reductions in seizure frequency and severity from baseline (all P < 0.05). When participants on CBD + clobazam were compared with CBD - clobazam, there were no significant differences in seizure frequency and severity reduction between the groups at 12 weeks (both P > 0.05). When comparing groups with iAEDs vs. group without iAEDs, independent of coadministration of clobazam, no differences in treatment response were observed (all P > 0.05). Longitudinal analyses up to 48 weeks after therapy initiation did not reveal any differences in treatment response between groups.<h4>Conclusion</h4>These analyses suggest that concomitant to CBD, AEDs may not have an effect on reducing seizure frequency and severity in patients with TRE.
The impediment to action advances action.