Brivaracetam effectiveness and tolerability in older and younger adults with epilepsy: EXPERIENCE, a pooled analysis of international data from retrospective studies

被引:2
作者
Faught, Edward [1 ]
Besson, Herve [2 ]
D'Souza, Wendyl [3 ]
Rosenow, Felix [6 ]
Klein, Pavel [4 ]
Reuber, Markus [5 ]
Insuga, Victor Soto
Salas-Puig, Javier [7 ]
Steinhoff, Bernhard J. [9 ,10 ]
Strzelczyk, Adam [6 ]
Szaflarski, Jerzy P. [11 ,12 ]
Bourikas, Dimitrios [13 ]
Daniels, Tony [14 ]
Laloyaux, Cedric [17 ]
Floricel, Florin [15 ]
Friesen, David [16 ]
Villanueva, Vicente [8 ,18 ]
机构
[1] Emory Univ, Emory Sleep Ctr, 12 Execut Pk Dr NE, Atlanta, GA 30329 USA
[2] UCB Pharm, Hoge Mosten 2, NL-4822 NH Breda, Netherlands
[3] Univ Melbourne, St Vincents Hosp Melbourne, Dept Med, 41 Victoria Parade, Melbourne, Vic 3065, Australia
[4] Midatlant Epilepsy & Sleep Ctr, 6410 Rockledge Dr,Suite 610, Bethesda, MD 20817 USA
[5] Univ Sheffield, Royal Hallamshire Hosp, Dept Neurosci, Acad Neurol Unit, Glossop Rd, Sheffield S10 2JF, England
[6] Goethe Univ Frankfurt, Univ Hosp Frankfurt, Epilepsy Ctr Frankfurt Rhine Main, Dept Neurol, Schleusenweg 2-16,Haus 95, D-60528 Frankfurt, Germany
[7] Univ Vall dHebron, Passeig Vall dHebron, 119-129, Barcelona 08035, Spain
[8] Hosp Univ Infantil Nino Jesus, Pediat Neurol, Ave Menendez Pelayo 65, Madrid 28009, Spain
[9] Univ Freiburg, Kork Epilepsy Ctr, Landstr 1,Breisacher Str 64, D-79106 Freiburg, Germany
[10] Univ Freiburg, Med Fac, Breisacher Str 64, D-79106 Freiburg, Germany
[11] Univ Alabama Birmingham, Dept Neurol, Heersink Sch Med, SC 350,1720 2nd Ave South, Birmingham, AL 35294 USA
[12] Univ Alabama Birmingham, UAB Epilepsy Ctr, Heersink Sch Med, SC 350,1720 2nd Ave South, Birmingham, AL 35294 USA
[13] UCB Pharma, Agiou Dimitriou 63, Alimos 17456, Greece
[14] UCB Pharm, 4000 Paramount Pkwy, Morrisville, NC 27560 USA
[15] UCB Pharm, Alfred Nobel Str 10, D-40789 Monheim, Germany
[16] UCB Pharm, 216 Bath Rd, Slough SL1 3WE, England
[17] UCB Pharm, Allee Rech 60, B-1070 Brussels, Belgium
[18] Hosp Univ & Politecn La Fe, Refractory Epilepsy Unit, Ave Fernando Abril Martorell 106, Valencia 46026, Spain
关键词
Adverse event; Antiseizure medication; Older adults; Real world; Retention; Seizure response; CLASSIFICATION; EFFICACY; SEIZURES; SAFETY; AUDIT;
D O I
10.1016/j.yebeh.2024.109922
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
This analysis assessed the effectiveness and tolerability of brivaracetam (BRV) in older (>= 65 years of age) and younger (>= 16 to <65 years of age) adults with epilepsy. This was a subgroup analysis from EXPERIENCE/ EPD332, a pooled analysis of individual patient records from multiple independent, non-interventional studies of patients with epilepsy starting BRV in Australia, Europe, and the United States. Included patients had >= 6 months of follow-up data. Outcomes included responders (>= 50 % reduction from baseline in seizure frequency), seizure freedom (no seizures within 3 months before the time point), and continuous seizure freedom (no seizures from baseline) at 12 months; BRV discontinuation during the whole study follow-up; and treatment-emergent adverse events (TEAEs) at 3, 6, and 12 months. Patients with missing data after BRV discontinuation were deemed nonresponders/not seizure-free. Analysis populations included the Full Analysis Set (FAS; patients who received >= 1 BRV dose and had seizure type and age documented at baseline) and the modified FAS (FAS patients who had >= 1 seizure recorded during baseline). The FAS was used for all outcomes except seizure reduction. The FAS included 147 (8.9 %) patients aged >= 65 years and 1497 (91.1 %) aged >= 16 to <65 years. Compared with the younger subgroup, patients aged >= 65 years had a longer median epilepsy duration (33.0 years [n = 144] vs 17.0 years [n = 1460]) and lower median seizure frequency at index (2.0 seizures/28 days [n = 129] vs 4.0 seizures/28 days [n = 1256]), and less commonly had >1 prior antiseizure medication (106/141 [75.2 %] vs 1265/1479 [85.5 %]). At 12 months, a numerically higher percentage of patients aged >= 65 years versus the younger subgroup achieved >= 50 % seizure reduction (46.5 % [n = 71] vs 36.0 % [n = 751]), seizure freedom (26.0 % [n = 100] vs 13.9 % [n = 1011]), and continuous seizure freedom (22.0 % [n = 100] vs 10.7 % [n = 1011]). During the whole study follow-up, 43/147 (29.3 %) patients aged >= 65 years and 508/1492 (34.0 %) aged >= 16 to <65 years discontinued BRV. The incidence of TEAEs since the prior visit was similar in both subgroups at 3 months ( >= 65 years vs >= 16 to <65 years: 38/138 [27.5 %] vs 356/1404 [25.4 %]), 6 months (19/119 [16.0 %] vs 176/1257 [14.0 %]), and 12 months (8/104 [7.7 %] vs 107/1128 [9.5 %]). This real-world analysis suggests BRV was effective in patients aged >= 65 years and >= 16 to <65 years, with numerically higher effectiveness in the older subgroup. BRV was well tolerated in both subgroups.
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