Strzelczyk Adam, Klotz Kerstin Alexandra, Mayer Thomas, von Podewils Felix, Knake Susanne, Kurlemann Gerhard, Herold Luise, Immisch Ilka, Buhleier Elisa, Rosenow Felix, Schubert-Bast Susanne
Goethe-University Frankfurt, Epilepsy Center Frankfurt Rhine-Main, Department of Neurology, University Medicine Frankfurt, Theodor-Stern-Kai 7, 60596, Frankfurt am Main, Germany.
Department of Pediatric Neurology, University Hospital Bonn, Bonn, Germany.
Neurol Ther. 2025 Jul 12. doi: 10.1007/s40120-025-00788-w.
Effectiveness and tolerability of plant-derived highly purified cannabidiol (CBD) in patients with Lennox-Gastaut syndrome (LGS), Dravet syndrome (DS), or tuberous sclerosis complex (TSC)-associated epilepsy in clinical practice in Germany were evaluated.
This multicenter, retrospective, chart review study analyzed patients with LGS, DS, or TSC-associated epilepsy receiving ≥ 1 dose of adjunctive CBD (Epidyolex 100 mg/mL oral solution). Treatment characteristics, seizure outcomes, physician-rated Clinical Global Impression of Change (CGI-C), treatment retention rates, and adverse events (AEs) were analyzed ≤ 12 months.
Among 202 patients identified (159 LGS; 34 DS; 9 TSC), median (interquartile range; range) age was 18.0 (7.9-32.0; 0.3-72.0) years, and median (range) number of prior and concomitant antiseizure medications was 6 (1-24) and 3 (1-7), respectively. Median target CBD dose was 11.1 mg/kg/day (17.6, 15.2, and 9.9 mg/kg/day in the < 6, 6-17, and ≥ 18 years subgroups, respectively). Responder rates (≥ 50% seizure reduction) for total seizures at 3 (n = 194) and 12 (n = 168) months were 43.3% (37.0-50.0% across ages) and 44.0% (37.0-52.5% across ages), respectively, and for generalized tonic-clonic seizures 54.3% (n = 94) (50.0-66.7% across ages) and 47.7% (n = 88) (37.8-66.7% across ages), respectively. Median (range) number of seizure days per month significantly decreased from 30 (0.3-30) to 18 (0-30) in the 3 months before the last 3 months of CBD treatment (p < 0.001). Any improvement in CGI-C was observed in 62% of patients. Of those with available data at 3 and 12 months, 89.6% and 67.1% remained on CBD, respectively. Retention was similar across age groups. AEs reported in ≥ 5% of patients were sedation and diarrhea.
In patients with LGS, DS, or TSC-associated epilepsy, adjunctive CBD was associated with a reduction in seizure frequency across age groups. CBD demonstrated tolerability consistent with its known profile, and 67% of patients remained on treatment at 12 months.
对德国临床实践中植物来源的高纯度大麻二酚(CBD)治疗Lennox-Gastaut综合征(LGS)、Dravet综合征(DS)或结节性硬化症(TSC)相关癫痫患者的有效性和耐受性进行了评估。
这项多中心、回顾性、病历审查研究分析了接受≥1剂辅助CBD(Epidyolex 100 mg/mL口服溶液)治疗的LGS、DS或TSC相关癫痫患者。分析了≤12个月的治疗特征、癫痫发作结局、医生评定的临床总体印象变化(CGI-C)、治疗保留率和不良事件(AE)。
在确定的202例患者中(159例LGS;34例DS;9例TSC),年龄中位数(四分位间距;范围)为18.0(7.9 - 32.0;0.3 - 72.0)岁,既往和同时使用的抗癫痫药物数量中位数(范围)分别为6(1 - 24)种和3(1 - 7)种。CBD目标剂量中位数为11.1 mg/kg/天(<6岁、6 - 17岁和≥18岁亚组分别为17.6、15.2和9.9 mg/kg/天)。3个月(n = 194)和12个月(n = 168)时,总癫痫发作的缓解率(癫痫发作减少≥50%)分别为43.3%(各年龄组为37.0 - 50.0%)和44.0%(各年龄组为37.0 - 52.5%),全身强直阵挛性发作的缓解率分别为54.3%(n = 94)(各年龄组为50.0 - 66.7%)和47.7%(n = 88)(各年龄组为37.8 - 66.7%)。在CBD治疗的最后3个月前的3个月内,每月癫痫发作天数中位数(范围)从30(0.3 - 30)显著降至18(0 - 30)(p<0.001)。62%的患者在CGI-C方面有任何改善。在3个月和12个月有可用数据的患者中,分别有89.6%和67.1%继续使用CBD。各年龄组的保留率相似。≥5%的患者报告的不良事件为镇静和腹泻。
在LGS、DS或TSC相关癫痫患者中,辅助使用CBD与各年龄组癫痫发作频率降低相关。CBD表现出与其已知特征相符的耐受性,12个月时67%的患者仍在接受治疗。