Efficacy of antiepileptic drugs in the adjunctive treatment of refractory partial-onset seizures: Meta-analysis of pivotal trials

•All 11 AEDs in this meta-analysis had greater seizure response vs placebo.•Pregabalin, tiagabine, and vigabatrin had the highest pooled odds of ≥50% seizure reduction.•Ezogabine, levetiracetam, and vigabatrin had the highest pooled odds of seizure freedom.•Patients were more likely to discontinue a...

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Veröffentlicht in:Epilepsy research 2018-07, Vol.143, p.120-129
Hauptverfasser: Slater, Jeremy, Chung, Steve, Huynh, Lynn, Duh, Mei Sheng, Gorin, Brian, McMicken, Carolyn, Ziemann, Adam, Isojarvi, Jouko
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container_start_page 120
container_title Epilepsy research
container_volume 143
creator Slater, Jeremy
Chung, Steve
Huynh, Lynn
Duh, Mei Sheng
Gorin, Brian
McMicken, Carolyn
Ziemann, Adam
Isojarvi, Jouko
description •All 11 AEDs in this meta-analysis had greater seizure response vs placebo.•Pregabalin, tiagabine, and vigabatrin had the highest pooled odds of ≥50% seizure reduction.•Ezogabine, levetiracetam, and vigabatrin had the highest pooled odds of seizure freedom.•Patients were more likely to discontinue any AED (except pregabalin) than placebo. In the absence of randomized clinical trials (RCTs) assessing the relative efficacy of antiepileptic drugs (AEDs), meta-analyses are useful resources for informing treatment choices. This meta-analysis assesses the relative efficacy and tolerability of AEDs for adjunctive treatment of refractory partial onset seizures (POS). A systematic literature review was conducted to identify pivotal AED trials serving as the basis for US Food and Drug Administration (FDA) approval. Inclusion criteria: 1) double-blind, placebo-controlled, parallel-group design, with 8- to 14-week maintenance period; 2) enrolled patients ≥16years with refractory POS, including complex partial seizures; 3) study was conducted between 1993 and 2013; and; 4) patients received FDA-approved dosage. Outcomes analyzed: 1) 50% responder rate (≥50% reduction from baseline in seizure frequency); 2) seizure freedom (proportion of seizure-free patients); and 3) discontinuation due to adverse events (AEs). DerSimonian and Laird random-effects model was used to derive odds ratios (OR) and 95% confidence intervals (CI). A total of 29 publications for 11 AEDs (eslicarbazepine, ezogabine, gabapentin, lacosamide, levetiracetam, perampanel, pregabalin, tiagabine, topiramate, vigabatrin, and zonisamide) were included in the meta-analysis. Tiagabine 56mg/day (OR 8.82, 95% CI: 2.77–28.11), pregabalin 600mg/day (OR 8.08, 95% CI: 5.45–11.98), and vigabatrin 3000mg/day (OR 6.23, 95% CI: 1.46–26.20) had the highest OR versus placebo of 50% response. The odds of seizure freedom were ≥7 times greater than placebo for levetiracetam 3000mg/day (OR 11.00, 95% CI: 2.08–58.06), vigabatrin 3000mg/day (OR 7.41, 95% CI: 1.31–41.84), and ezogabine 1200mg/day (OR 7.09, 95% CI: 0.36–58.06). Patients were more likely to discontinue any AED (except low-dose pregabalin) than placebo. In this meta-analysis of >9000 patients, those treated with AEDs were more likely than placebo to achieve seizure response or freedom. Patients receiving pregabalin, tiagabine, and vigabatrin had the highest odds of ≥50% reduction in seizures, and patients receiving ezogabine, levetiracetam, and vigabatrin had th
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In the absence of randomized clinical trials (RCTs) assessing the relative efficacy of antiepileptic drugs (AEDs), meta-analyses are useful resources for informing treatment choices. This meta-analysis assesses the relative efficacy and tolerability of AEDs for adjunctive treatment of refractory partial onset seizures (POS). A systematic literature review was conducted to identify pivotal AED trials serving as the basis for US Food and Drug Administration (FDA) approval. Inclusion criteria: 1) double-blind, placebo-controlled, parallel-group design, with 8- to 14-week maintenance period; 2) enrolled patients ≥16years with refractory POS, including complex partial seizures; 3) study was conducted between 1993 and 2013; and; 4) patients received FDA-approved dosage. Outcomes analyzed: 1) 50% responder rate (≥50% reduction from baseline in seizure frequency); 2) seizure freedom (proportion of seizure-free patients); and 3) discontinuation due to adverse events (AEs). DerSimonian and Laird random-effects model was used to derive odds ratios (OR) and 95% confidence intervals (CI). A total of 29 publications for 11 AEDs (eslicarbazepine, ezogabine, gabapentin, lacosamide, levetiracetam, perampanel, pregabalin, tiagabine, topiramate, vigabatrin, and zonisamide) were included in the meta-analysis. Tiagabine 56mg/day (OR 8.82, 95% CI: 2.77–28.11), pregabalin 600mg/day (OR 8.08, 95% CI: 5.45–11.98), and vigabatrin 3000mg/day (OR 6.23, 95% CI: 1.46–26.20) had the highest OR versus placebo of 50% response. The odds of seizure freedom were ≥7 times greater than placebo for levetiracetam 3000mg/day (OR 11.00, 95% CI: 2.08–58.06), vigabatrin 3000mg/day (OR 7.41, 95% CI: 1.31–41.84), and ezogabine 1200mg/day (OR 7.09, 95% CI: 0.36–58.06). Patients were more likely to discontinue any AED (except low-dose pregabalin) than placebo. In this meta-analysis of &gt;9000 patients, those treated with AEDs were more likely than placebo to achieve seizure response or freedom. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-7233b557830d6082c481de63f21670d79f0713111d9ae62a3216943512848383</citedby><cites>FETCH-LOGICAL-c490t-7233b557830d6082c481de63f21670d79f0713111d9ae62a3216943512848383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.eplepsyres.2017.10.004$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29784458$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Slater, Jeremy</creatorcontrib><creatorcontrib>Chung, Steve</creatorcontrib><creatorcontrib>Huynh, Lynn</creatorcontrib><creatorcontrib>Duh, Mei Sheng</creatorcontrib><creatorcontrib>Gorin, Brian</creatorcontrib><creatorcontrib>McMicken, Carolyn</creatorcontrib><creatorcontrib>Ziemann, Adam</creatorcontrib><creatorcontrib>Isojarvi, Jouko</creatorcontrib><title>Efficacy of antiepileptic drugs in the adjunctive treatment of refractory partial-onset seizures: Meta-analysis of pivotal trials</title><title>Epilepsy research</title><addtitle>Epilepsy Res</addtitle><description>•All 11 AEDs in this meta-analysis had greater seizure response vs placebo.•Pregabalin, tiagabine, and vigabatrin had the highest pooled odds of ≥50% seizure reduction.•Ezogabine, levetiracetam, and vigabatrin had the highest pooled odds of seizure freedom.•Patients were more likely to discontinue any AED (except pregabalin) than placebo. In the absence of randomized clinical trials (RCTs) assessing the relative efficacy of antiepileptic drugs (AEDs), meta-analyses are useful resources for informing treatment choices. This meta-analysis assesses the relative efficacy and tolerability of AEDs for adjunctive treatment of refractory partial onset seizures (POS). A systematic literature review was conducted to identify pivotal AED trials serving as the basis for US Food and Drug Administration (FDA) approval. Inclusion criteria: 1) double-blind, placebo-controlled, parallel-group design, with 8- to 14-week maintenance period; 2) enrolled patients ≥16years with refractory POS, including complex partial seizures; 3) study was conducted between 1993 and 2013; and; 4) patients received FDA-approved dosage. Outcomes analyzed: 1) 50% responder rate (≥50% reduction from baseline in seizure frequency); 2) seizure freedom (proportion of seizure-free patients); and 3) discontinuation due to adverse events (AEs). DerSimonian and Laird random-effects model was used to derive odds ratios (OR) and 95% confidence intervals (CI). A total of 29 publications for 11 AEDs (eslicarbazepine, ezogabine, gabapentin, lacosamide, levetiracetam, perampanel, pregabalin, tiagabine, topiramate, vigabatrin, and zonisamide) were included in the meta-analysis. Tiagabine 56mg/day (OR 8.82, 95% CI: 2.77–28.11), pregabalin 600mg/day (OR 8.08, 95% CI: 5.45–11.98), and vigabatrin 3000mg/day (OR 6.23, 95% CI: 1.46–26.20) had the highest OR versus placebo of 50% response. The odds of seizure freedom were ≥7 times greater than placebo for levetiracetam 3000mg/day (OR 11.00, 95% CI: 2.08–58.06), vigabatrin 3000mg/day (OR 7.41, 95% CI: 1.31–41.84), and ezogabine 1200mg/day (OR 7.09, 95% CI: 0.36–58.06). Patients were more likely to discontinue any AED (except low-dose pregabalin) than placebo. In this meta-analysis of &gt;9000 patients, those treated with AEDs were more likely than placebo to achieve seizure response or freedom. 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In the absence of randomized clinical trials (RCTs) assessing the relative efficacy of antiepileptic drugs (AEDs), meta-analyses are useful resources for informing treatment choices. This meta-analysis assesses the relative efficacy and tolerability of AEDs for adjunctive treatment of refractory partial onset seizures (POS). A systematic literature review was conducted to identify pivotal AED trials serving as the basis for US Food and Drug Administration (FDA) approval. Inclusion criteria: 1) double-blind, placebo-controlled, parallel-group design, with 8- to 14-week maintenance period; 2) enrolled patients ≥16years with refractory POS, including complex partial seizures; 3) study was conducted between 1993 and 2013; and; 4) patients received FDA-approved dosage. Outcomes analyzed: 1) 50% responder rate (≥50% reduction from baseline in seizure frequency); 2) seizure freedom (proportion of seizure-free patients); and 3) discontinuation due to adverse events (AEs). DerSimonian and Laird random-effects model was used to derive odds ratios (OR) and 95% confidence intervals (CI). A total of 29 publications for 11 AEDs (eslicarbazepine, ezogabine, gabapentin, lacosamide, levetiracetam, perampanel, pregabalin, tiagabine, topiramate, vigabatrin, and zonisamide) were included in the meta-analysis. Tiagabine 56mg/day (OR 8.82, 95% CI: 2.77–28.11), pregabalin 600mg/day (OR 8.08, 95% CI: 5.45–11.98), and vigabatrin 3000mg/day (OR 6.23, 95% CI: 1.46–26.20) had the highest OR versus placebo of 50% response. The odds of seizure freedom were ≥7 times greater than placebo for levetiracetam 3000mg/day (OR 11.00, 95% CI: 2.08–58.06), vigabatrin 3000mg/day (OR 7.41, 95% CI: 1.31–41.84), and ezogabine 1200mg/day (OR 7.09, 95% CI: 0.36–58.06). Patients were more likely to discontinue any AED (except low-dose pregabalin) than placebo. In this meta-analysis of &gt;9000 patients, those treated with AEDs were more likely than placebo to achieve seizure response or freedom. Patients receiving pregabalin, tiagabine, and vigabatrin had the highest odds of ≥50% reduction in seizures, and patients receiving ezogabine, levetiracetam, and vigabatrin had the highest odds of seizure freedom.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>29784458</pmid><doi>10.1016/j.eplepsyres.2017.10.004</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals
subjects AEDs
Anticonvulsants - therapeutic use
Antiepileptic drugs
Chemotherapy, Adjuvant
Drug Resistance
Drug Resistant Epilepsy - drug therapy
Epilepsies, Partial - drug therapy
Humans
Meta-analysis
Refractory partial-onset seizures
rPOS
Seizures - drug therapy
title Efficacy of antiepileptic drugs in the adjunctive treatment of refractory partial-onset seizures: Meta-analysis of pivotal trials
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