Long-term cannabidiol treatment for seizures in patients with tuberous sclerosis complex: An open-label extension trial

被引:56
作者
Thiele, Elizabeth A. [1 ]
Bebin, E. Martina [2 ]
Filloux, Francis [3 ]
Kwan, Patrick [4 ,5 ]
Loftus, Rachael [6 ]
Sahebkar, Farhad [7 ]
Sparagana, Steven [8 ,9 ]
Wheless, James [10 ,11 ]
机构
[1] Massachusetts Gen Hosp, Boston, MA 02114 USA
[2] Univ Alabama Birmingham, Sch Med, Birmingham, AL USA
[3] Univ Utah, Sch Med, Salt Lake City, UT USA
[4] Monash Univ, Melbourne, Vic, Australia
[5] Univ Melbourne, Melbourne, Vic, Australia
[6] GW Res Ltd, Cambridge, England
[7] Greenwich Biosci Inc, Carlsbad, CA USA
[8] Scottish Rite Children, Dallas, TX USA
[9] Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA
[10] Le Bonheur Childrens Hosp, Memphis, TN USA
[11] Univ Tennessee, Hlth Sci Ctr, Memphis, TN USA
关键词
antiseizure medication; cannabidiol; epilepsy; focal seizures; treatment-resistant epilepsy; tuberous sclerosis complex; VAGUS NERVE-STIMULATION; REFRACTORY EPILEPSY; DOUBLE-BLIND; MANAGEMENT; PHASE-3;
D O I
10.1111/epi.17150
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To evaluate the long-term safety and efficacy of add-on cannabidiol (CBD) in patients with seizures associated with tuberous sclerosis complex (TSC) in the open-label extension (OLE) of the randomized, placebo-controlled phase 3 trial GWPCARE6 (NCT02544763). Results of an interim (February 2019 data cut) analysis are reported. Methods Patients who completed the randomized trial enrolled to receive CBD (Epidiolex(R) in the United States; Epidyolex(R) in the EU; 100 mg/mL oral solution). The initial target dose was 25 mg/kg/day, which, based on response and tolerability, could be decreased or increased up to 50 mg/kg/day. The primary end point was safety. Key secondary end points included percentage reduction in TSC-associated (countable focal and generalized) seizures, responder rates, and Subject/Caregiver Global Impression of Change (S/CGIC). Results Of 201 patients who completed the randomized phase, 199 (99%) entered the OLE. Mean age was 13 years (range, 1-57). At the time of analysis, 5% of patients had completed treatment, 20% had withdrawn, and 75% were ongoing. One-year retention rate was 79%. Median treatment time was 267 days (range, 18-910) at a 27 mg/kg/day mean modal dose. Most patients (92%) had an adverse event (AE). Most common AEs were diarrhea (42%), seizure (22%), and decreased appetite (20%). AEs led to permanent discontinuation in 6% of patients. There was one death that was deemed treatment unrelated by the investigator. Elevated liver transaminases occurred in 17 patients (9%) patients; 12 were taking valproate. Median percentage reductions in seizure frequency (12-week windows across 48 weeks) were 54%-68%. Seizure responder rates (>= 50%, >= 75%, 100% reduction) were 53%-61%, 29%-45%, and 6%-11% across 12-week windows for 48 weeks. Improvement on the S/CGIC scale was reported by 87% of patients/caregivers at 26 weeks. Significance In patients with TSC, long-term add-on CBD treatment was well tolerated and sustainably reduced seizures through 48 weeks, with most patients/caregivers reporting global improvement.
引用
收藏
页码:426 / 439
页数:14
相关论文
共 39 条
[1]   Causes of mortality in individuals with tuberous sclerosis complex [J].
Amin, Sam ;
Lux, Andrew ;
Calder, Nuala ;
Laugharne, Matthew ;
Osborne, John ;
O'callaghan, Finbar .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2017, 59 (06) :612-617
[2]  
[Anonymous], 2021, EPIDIOLEX CANN OR SO
[3]  
[Anonymous], 2021, EPIDYOLEX CANNABIDIO
[4]   Pathogenesis of tuberous sclerosis subependymal giant cell astrocytornas:: Biallelic inactivation of TSC1 or TSC2 leads to rnTOR activation [J].
Chan, JA ;
Zhang, HB ;
Roberts, PS ;
Jozwiak, S ;
Wieslawa, G ;
Lewin-Kowalik, J ;
Kotulska, K ;
Kwiatkowski, DJ .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2004, 63 (12) :1236-1242
[5]   The natural history of epilepsy in tuberous sclerosis complex [J].
Chu-Shore, Catherine J. ;
Major, Philippe ;
Camposano, Susana ;
Muzykewicz, David ;
Thiele, Elizabeth A. .
EPILEPSIA, 2010, 51 (07) :1236-1241
[6]   The tuberous sclerosis complex [J].
Crino, Peter B. ;
Nathanson, Katherine L. ;
Henske, Elizabeth Petri .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (13) :1345-1356
[7]   Tuberous sclerosis [J].
Curatolo, Paolo ;
Bombardieri, Roberta ;
Jozwiak, Sergiusz .
LANCET, 2008, 372 (9639) :657-668
[8]   Management of epilepsy associated with tuberous sclerosis complex: Updated clinical recommendations [J].
Curatolo, Paolo ;
Nabbout, Rima ;
Lagae, Lieven ;
Aronica, Eleonora ;
Ferreira, Jose Carlos ;
Feucht, Martha ;
Hertzberg, Christoph ;
Jansen, Anna C. ;
Jansen, Floor ;
Kotulska, Katarzyna ;
Moavero, Romina ;
O'Callaghan, Finbar ;
Papavasiliou, Antigone ;
Tzadok, Michal ;
Jozwiak, Sergiusz .
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2018, 22 (05) :738-748
[9]   Neurological and neuropsychiatric aspects of tuberous sclerosis complex [J].
Curatolo, Paolo ;
Moavero, Romina ;
de Vries, Petrus J. .
LANCET NEUROLOGY, 2015, 14 (07) :733-745
[10]   Management of epilepsy associated with tuberous sclerosis complex (TSC): Clinical recommendations [J].
Curatolo, Paolo ;
Jozwiak, Sergiusz ;
Nabbout, Rima .
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2012, 16 (06) :582-586