Front. Pharmacol. Frontiers in Pharmacology Front. Pharmacol. 1663-9812 Frontiers Media S.A. 1500475 10.3389/fphar.2025.1500475 Pharmacology Systematic Review Effectiveness and safety of single anti-seizure medication as adjunctive therapy for drug-resistant focal epilepsy based on network meta-analysis Deng et al. 10.3389/fphar.2025.1500475 Deng Nian-Jia 1 Li Xin-Yi 1 Zhang Zhi-Xin 1 Xian-Yu Chen-Yang 1 Tao Yu-Ting 1 Ma Yu-Tong 1 Li Hui-Jun 1 Gao Teng-Yu 1 Liu Xin 1 Luo Jie 1 2 * Zhang Chao 1 * Hu Sheng-Li 2 * 1 Center for Evidence-Based Medicine and Clinical Research, Hubei Provincial Clinical Research Center of Central Nervous System Repair and Functional Reconstruction, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, China 2 Department of Neurosurgery, Hubei Provincial Clinical Research Center of Central Nervous System Repair and Functional Reconstruction, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, China

Edited by: Hua-Jun Feng, Massachusetts General Hospital and Harvard Medical School, United States

Reviewed by: Angelo Russo, IRCCS Institute of Neurological Sciences of Bologna (ISNB), Italy

Vishal Sondhi, Armed Forces Medical College, India

 *Correspondence: Jie Luo, taihehospital@yeah.net; Chao Zhang, zhangchao0803@126.com; Sheng-Li Hu, hushengliwu@163.com 25 04 2025 2025 16 1500475 23 09 2024 14 04 2025 Copyright © 2025 Deng, Li, Zhang, Xian-Yu, Tao, Ma, Li, Gao, Liu, Luo, Zhang and Hu. 2025 Deng, Li, Zhang, Xian-Yu, Tao, Ma, Li, Gao, Liu, Luo, Zhang and Hu

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 Objective

To evaluated the effectiveness and safety of single anti-seizure medication (ASM) when used as adjunctive therapy for drug-resistant focal epilepsy.

 Methods

We conducted a comprehensive search of PubMed, EMbase, and the Cochrane Library from their inception until 12 February, 2025, to identify randomized controlled trials (RCTs) meeting our criteria. The trials were analyzed for their use of ASMs in treating drug-resistant focal epilepsy. Inclusion criteria comprised: 1) Participants aged 12 years or older with drug-resistant focal epilepsy; 2) Incorporation of an additional single ASM as an adjunct to the existing antiepileptic treatment regimen; 3) Comparison with placebo or continuation of the original antiepileptic regimen without a new ASM; 4) Primary outcome as a 50% response rate, with safety as a secondary outcome, encompassing dizziness, somnolence, headache, ataxia, diplopia, fatigue, and nausea; and 5) Study design limited to RCTs. The surface under the cumulative ranking curve (SUCRA) was employed to rank the effectiveness and safety of the ASMs.

 Results

A total of 53 RCTs involving 17 ASMs as adjunctive therapy and placebo were analyzed. Compared to placebo, the following ASMs demonstrated statistically significant effectiveness in achieving a 50% response rate: brivaracetam (RR = 2.07, 95% CI: 1.53–2.81), cenobamate (RR = 2.12, 95% CI: 1.56–2.88), eslicarbazepine acetate (RR = 1.95, 95% CI: 1.41–2.70), gabapentin (RR = 2.30, 95% CI: 1.76–3.02), lacosamide (RR = 2.22, 95% CI: 1.47–3.35), lamotrigine (RR = 1.55, 95% CI: 1.00–2.40), levetiracetam (RR = 2.43, 95% CI: 1.88–3.15), oxcarbazepine (RR = 3.03, 95% CI: 2.08–4.40), perampanel (RR = 1.72, 95% CI: 1.21–2.44), pregabalin (RR = 2.06, 95% CI: 1.70–2.50), rufinamide (RR = 2.28, 95% CI: 1.20–4.31), tiagabine (RR = 4.07, 95% CI: 2.03–8.18), topiramate (RR = 3.10, 95% CI: 2.44–3.95), vigabatrin (RR = 2.34, 95% CI: 1.58–3.46), and zonisamide (RR = 2.40, 95% CI: 1.76–3.27). Based on SUCRA rankings, tiagabine (92.7%) exhibited the most favorable therapeutic outcome, followed by topiramate (87.3%), oxcarbazepine (83%), and levetiracetam (62.8%). The ASMs with the least favorable therapeutic effects were placebo (1.1%), lamotrigine (17.8%), and perampanel (24.7%).

 Conclusion

The network meta-analysis revealed topiramate, tiagabine, oxcarbazepine, and levetiracetam as the four most effective adjuvant ASM treatments for drug-resistant focal epilepsy. However, it is noteworthy that topiramate and oxcarbazepine were associated with a higher incidence of somnolence. Additionally, comprehensive safety data for tiagabine and levetiracetam are lacking, necessitating further research. Larger studies are required to solidify these findings and better understand the safety profiles of all involved ASMs.

 drug-resistant focal seizures anti-seizure medication topiramate levetiracetam gabapentin pregabalin section-at-acceptance Neuropharmacology Introduction

Epilepsy was stands as one of the most prevalent brain disorders worldwide, impacting over 70 million individuals across all age groups, from infants and young children to the elderly, to varying degrees. The most frequent form of epilepsy in humans was focal epilepsy, which comprises more than half of all cases and poses the greatest therapeutic challenge when treated with anti-epileptic medications (Gooley et al., 2022; Engel, 2004). Focal seizures typically originated in a confined area of the cerebral cortex and subsequently propagate to adjacent regions, encompassing both the surrounding cortical tissue and subcutaneous structures (Jenssen et al., 2011). The most typical pathological conditions associated with focal epilepsy include traumatic brain injuries, tumors, and vascular malformations (Bernasconi and Bernasconi, 2022). Meanwhile, drug-resistant epilepsy referred to cases where seizures persist despite adjustments to anti-seizure medication (ASM) therapy, rendering seizure freedom highly improbable with further pharmacological interventions.

Over the past few decades, remarkable progress had been achieved in the treatment of epilepsy, with approximately 30 ASMs now clinically available. These ASMs had played a pivotal role in decreasing the frequency and severity of seizures, ultimately enhancing the quality of life for epilepsy patients (Löscher and Klein, 2021). A study revealed that topiramate, levetiracetam, pregabalin, and oxcarbazepine offered advantages over other ASMs in terms of adverse reactions and treatment risks. Conversely, rufinamide demonstrated suboptimal treatment effectiveness and a high risk of severe, urgent headaches (Zhao et al., 2017). Another meta-analysis (Hu et al., 2018) found that brivaracetam, levetiracetam, oxcarbazepine, vigabatrin, and topiramate exhibited reliable effectiveness, with levetiracetam being the most well-tolerated. Additionally, the study suggested that levetiracetam, vigabatrin, and gabapentin offered the best balance of short-term effectiveness and tolerability, while oxcarbazepine was effective but poorly tolerated (Bodalia et al., 2013). Despite consistent findings highlighted levetiracetam’s effectiveness, the efficacy of other ASMs as adjunctive therapy remained controversial due to factors such as limited sample sizes, unclear outcome definitions, and variations in patient populations. To provided clinicians with more authoritative and efficient guidelines, an updated and comprehensive network meta-analysis was conducted to evaluate the effectiveness and safety of adding a new single ASM to an existing anti-epileptic regimen for drug-resistant focal epilepsy among the various available options.

 Methods

This study was conducted in accordance with the extended Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines specifically tailored for network meta-analyses of healthcare interventions (Hutton et al., 2015).

Search strategy

As of 12 February, 2025, we involved a network meta-analysis by searching to identify related RCTs in the PubMed, EMbase and Cochrane Library. The MeSH and keywords used in the search were “drug-resistant,” “medication-resistant,” “intractable,” “refractory,” “uncontrolled,” “drug refractory,” “pharmacoresistant,” “complex,” “partial,” “partial-onset,” “focal,” “epilepsy,” “seizure,” and “randomized controlled trial.” The literature search strategies were showed in Supplementary Method S1.

 Inclusion and exclusion criteria

The inclusion criteria were as follows: 1) Population: Participants with drug-resistant focal epilepsy (age ≥12 years). 2) Intervention: Incorporating an additional single ASM as an adjunct to the existing antiepileptic treatment regimen. 3) Comparison: Placebo or no new ASM as adjunctive therapy to an existing anti-epileptic regimen. 4) Outcomes: All studies included at least one effectiveness or safety outcomes. Effectiveness outcome was defined as 50% response rate, and was used as the primary outcome. Safety outcomes were used as the secondary outcomes, including dizziness, somnolence, headache, ataxia, diplopia, fatigue and nausea. 5) Study designs: Randomised controlled trials (RCTs).

The exclusion criteria included duplicate studies, no specific descriptions of ASMs as adjunctive therapy, studies with missing data, conference proceedings, and publications that are solely accessible in the abstract form.

 Data collection and processing

Five authors (Nian-Jia Deng, Xin-Yi Li, Zhi-Xin Zhang, Chen-Yang Xian-Yu, Yu-Ting Tao), in consensus, independently filtrate the literature and strictly extracted data in accordance with the predetermined inclusion criteria. Any potential conflicts or differences of opinion among the authors were resolved through a process of deliberation and consultation involving a fourth author (Yu-Tong Ma). The fundamental information of each study was extracted, including the year, sex ratio of participants, mean age, median duration of epilepsy (years), main inclusion criteria, comparison measures, and sample size.

 Quality assessment

Two reviewers independently assessed the risk of bias of the included studies (RoB-2) (Sterne et al., 2019). The RoB-2 evaluated studies in five domains: bias arising from the randomization process, bias due to deviations from intended interventions, bias due to missing outcome data, bias in outcome measurements, and bias in the selection of the reported results. There were “yes,” “probably yes,” “probably no,” “no,” and “no information” to answer the signal questions in the above domains. Notably, the consequences for bias risk were the same for “yes” and “probably yes” replies as they were for “no” and “probably no”. Additionally, the “probably” versions would typically imply that a judgment had been made. Following the completion of the signaling questions, a risk-of-bias assessment was made, and each domain was given one of three levels: low risk of bias, some concerns or high risk of bias.

 Statistical analysis

All dichotomous outcomes were employed for relative risk (RR) with 95% confidence intervals (CI), with a significant level of P < 0.05. I2 was used to detect the magnitude of heterogeneity. Additionally, the I2 statistic was used, where I2 values of ≥40% were indicative of significant heterogeneity (Higgins and James, 2011), the random effects model was employed. Otherwise, the fixed effects model was used. Network meta-analyses offer trustworthy proof for both direct and indirect comparisons of many interventions (Lu and Ades, 2004). The “loop inconsistency” method was employed for test of consistency equations when the treatment effects around a loop (Song et al., 2011). By definition, the surface under the cumulative ranking curve (SUCRA) values reflect the effectiveness and safety of ASMs as adjunctive therapy; thus, a rank plot with larger SUCRA scores implies more effective or safe ASMs as adjunctive therapy (Rücker and Schwarzer, 2015). Furthermore, a network funnel plot was used to detect any potential publication bias. All statistical analyses were conducted using STATA 15.0 and R 4.2.2, and it obtained a copyright license.

 Results Search results

In total, 5,303 relevant studies were retrieved, of which 1,759 were removed as duplicates. For participants who met the diagnostic standard for drug-resistant focal epilepsy, quantitative data was obtained for the network meta-analysis by scrutinizing the relevant literature titles, abstracts and full-text evaluations. Finally, a total of 53 studies comprising 13,700 participants with 17 ASMs as adjunctive therapy and placebo were involved in this study (Figure 1).

Study selection.

 Basic characteristics and quality assessment

Table 1 showed the primary attributes characteristics of the included studies, incorporating the quantity of study (n = 53), study year, sex ratio of participants, mean age, median duration of epilepsy (years), main inclusion criteria, comparison measures, and sample size. Active ASMs as adjunctive therapy, including brivaracetam, cenobamate, eslicarbazepine acetate, gabapentin, lacosamide, lamotrigine, levetiracetam, natalizumab, oxcarbazepine, perampanel, pregabalin, remacemid, rufinamide, tiagabine, topiramate, vigabatrin and zonisamide were incorporated in the network meta-analysis. An assessment of the risk of bias from randomized trials was conducted utilizing the latest RoB-2 assessment tool (Supplementary Table S1).

Basic information of included studies.

Study Year PMID Main inclusion criteria Comparisons Sample Male (%) Age, mean (range) Duration of epilepsy (year)
Anhut 1994 8082624 ≥12 years, 40–110 kg were eligible, as were women of childbearing potential using an adequate form of contraception. Patients with partial seizures who failed to respond to standard ASM therapy at maximum tolerated dosages were eligible for this study. Specifically, patients had an average of four clearly recognizable partial seizures per month during the 3 months before screening, despite treatment with one or two currently available ASMs. The dosage of these ASMs was stable during the 3 months before screening Placebo 109 56.2 12–67 >19
Gabapentin 900 mg/day 111 21
Gabapentin 1,200 mg/day 52 14
Arroyo 2004 14692903 ≥18 years, 50–135 kg, with the International League Against Epilepsy–defined partial seizures were allowed to enter Placebo 96 50.5 17–73 22.78 ± 13.58
Pregabalin 150 mg/day 99 24.8 ± 12.65
Pregabalin 600 mg/day 92 25.06 ± 11.63
Barcs 2000 11114219 Men and women aged 15–65 years were eligible. Patients had to experience an average of at least four partial seizures per month during the 8-week baseline phase preceding the double-blind treatment phase while maintained on one to three concomitant ASMs Placebo 173 44.5 34.3 (15–65) NA
Oxcarbazepine 600 mg/day 168 51.2 34.6 (15–65) NA
Oxcarbazepine 1,200 mg/day 177 45.2 33.8 (16–64) NA
Oxcarbazepine 2,400 mg/day 174 56.3 35.2 (15–66) NA
Baulac 2010 20696552 Men and nonpregnant, nonlactating women, ≥18 years of age, ≥40 kg, with a diagnosis of epilepsy with partial seizures were enrolled in the study. Diagnosis of epilepsy must have been consistent with results of an electroencephalogram performed within 2 years prior to randomization. The patients’ partial seizures had to be refractory to treatment Placebo 140 55 (39.3) 39.1 (11.2) 23.4 (12.2)
Pregabalin 300/600 mg/day 152 78 (51.3) 39.8 (11.2) 23.1 (13.5)
Lamotrigine 300/400 mg/day 141 77 (54.6) 39.4 (11.4) 23.1 (13.6)
Ben-Menachem 1996 8641230 Men and women aged 18–65 years with a history of partial seizures which had not responded to treatment with one or two ASMs were selected for entry into the baseline phase of the study. Patients had to have at least eight partial seizures during the 8-week baseline period while maintained on therapeutic doses and plasma concentrations of one or two appropriate ASMs. During this phase, the longest allowable seizure-free period was 3 weeks, and only one such period was permitted Placebo 28 84 37.2 NA
Topiramate 800 mg/day 28 NA
Ben-Menachem 1997 9092955 Patients between 18 and 65 years of age who were experiencing four or more seizures per month while receiving one or two standard ASMs during an 8-week baseline period were eligible for randomization to add-on therapy with Topiramate or placebo Placebo 24 NA 30 NA
Topiramate 400 mg/day 23 31
Placebo 30 30
Topiramate 600 mg/day 30 31
Placebo 28 36
Topiramate 800 mg/day 28 40
Ben-Menachem 2010 20299189 ≥18 years, assessed as being in general good health; diagnosed with simple or complex partial-onset seizures (with or without secondary generalization) for a minimum of 12 months prior to screening Placebo 100 49.1 18–69 25.4 ± 13.06
Eslicarbazepine acetate 400 mg/day 96 24.7 ± 11.52
Eslicarbazepine acetate 800 mg/day 101 22.4 ± 11.63
Eslicarbazepine acetate 1,200 mg/day 98 23.0 ± 12.90
Beydoun 2005 15699378 ≥18 years, 50–135 kg, with inadequately controlled partial-onset seizures diagnosed by patient history and a recent EEG (within the preceding 2 years). To be eligible, patients had to experience a minimum of six partial-onset seizures during a prospective 8-week baseline period, with no 28-day seizure-free period, while maintained on stable doses of one to three ASMs. Patients also had to have failed two or more ASMs at maximally tolerated doses Placebo 98 50 17–82 23.5 ± 11.9
Pregabalin 600 mg/day 215 26.8 ± 13.0
Biton 2011 20887365 Eligible patients were male or female, aged 12–80 years. Those who had ≧6 seizures during the 56 days, with no 21-day seizure free periods, were eligible for randomization into the double-blind phase of the study Placebo 175 83 38.1 NA
Rufinamide 3,200 mg/day 160 84 36.4 NA
Brodie 2004 15511696 18–59 years had a history of refractory partial seizures (at least four seizures per month in the previous 4 months), and were being treated with one or two ASMs, but not more than two of the following: phenytoin, carbamazepine, sodium valproate, phenobarbital, or primidone. In addition, patients had to be capable of counting the number of seizures that they experienced, because their record of seizure activity was an important component of the study data Placebo 71 59 18–59 NA
Zonisamide 400 mg/day 73 NA
Brodie 2005 15660766 ≥12 years, with partial seizures with or without secondary generalization unsatisfactorily controlled despite a stable regimen of one to three ASMs. Seizures were classified according to International League Against Epilepsy (ILAE) criteria into simple partial (SP) seizures, complex partial (CP) seizures, and partial seizures with secondary generalization (SGS) Placebo 120 57.6 12–77 20.4 (1.8–48.8)
Zonisamide 100 mg/day 56 23.4 (0.42–56)
Zonisamide 300 mg/day 55 15.7 (0.56–55.8)
Zonisamide 500 mg/day 118 18.9 (0.92–64.7)
Bruni 2000 10777431 16–50 years, with a definite diagnosis of complex partial seizures or partial seizures with secondary generalization were entered. This diagnosis was confirmed by documented focal EEG abnormalities. Patients were required to have a minimum of six complex partial seizures or partial seizures secondarily generalized over the 8-week period preceding entry Placebo 53 55 18–50 19 ± 1.4
Vigabatrin 3,000 mg/day 58 21 ± 1.2
Cereghino 2000 10908898 16–70 years, experienced uncontrolled partial seizures with or without becoming secondarily generalized for at least 2 years. Patients had to have a minimum of 12 partial seizures within 12 weeks before study selection, with a minimum of two partial seizures occurring per 4 weeks during the baseline period. Patients must have received at least two marketed ASMs, either simultaneously or consecutively Placebo 95 60.5 16–70 >2
Levetiracetam 1,000 mg/day 98
Levetiracetam 3,000 mg/day 101
Chadwick 2000 11162751 This was a two-center, double-blind, randomized, three-way parallel group comparison of adjunctive remacemide hydrochloride, and placebo, over 28 days, in patients with epilepsy Placebo 14 85.7% 40.4 (23–66) 21.9 (4–54)
Remacemide 300 mg/day 13 69.2% 36.3 (20–53) 23.5 (4–41)
Remacemide 400 mg/day 13 92.3% 36.2 (22–60) 22.2 (4–40)
Chung 2020 32409485 Patients were adults 18–65 years of age with a diagnosis of treatment-resistant focal (partial-onset) epilepsy, as defined by the International League Against Epilepsy. All seizure diagnoses were confirmed by an independent review from The Epilepsy Study Consortium. Patients must have been taking 1 to 3 ASMs at stable doses for at least 12 weeks before randomization Placebo 109 58 (53.2) 38 (18, 59) 21.1 (24.2, 60.75)
Cenobamate 200 mg/day 113 55 (48.7) 36 (18, 61) 19.95 (2.33, 52.5)
Faught 1997 9092954 18–65 years patients were required to have experienced at least four seizures per month during a 3-month baseline period while receiving one or two standard ASMs at therapeutic levels Placebo 45 80 34 NA
Topiramate 200 mg/day 45 NA
Topiramate 400 mg/day 42 NA
Topiramate 600 mg/day 43 NA
Faught 1997 Placebo 47 NA
Topiramate 600 mg/day 44 NA
Topiramate 800 mg/day 44 NA
Topiramate 1,000 mg/day 42 NA
Faught 1996 8649570 18–65 years patients were further required to have experienced at least 12 partial seizures during the 12-week baseline period preceding the double-blind study phase while maintained at therapeutic ASM plasma concentrations Placebo 45 80 36.2 (19–68) NA
Topiramate 200 mg/day 45 64.4 38.6 (19–67) NA
Topiramate 400 mg/day 45 86.7 38.9 (19–61) NA
Topiramate 600 mg/day 46 84.8 33.8 (20–58) NA
French 1996 8559421 18–60 years, with a diagnosis of complex partial seizures, with or without secondary generalization, whose seizures had been unsatisfactorily controlled with currently available anti-epilepsy medication, were eligible for participation in the study. Eligibility required that all patients studied had at least six documented complex partial seizures during the last 8 weeks of a 12-week pre-study screening period, despite a stable regimen of treatment of at least one, but not more than two, currently available anti-epileptic agents Placebo 90 44 18–60 NA
Vigabatrin 3,000 mg/day 92 NA
French 2003 12771254 12–70 years, had experienced at least three observable partial seizures in the month prior to screening and six partial seizures in the 8 weeks between screening and baseline; their disease was refractory to at least two ASMs at maximally tolerated doses; and they were currently receiving at least one but no more than three ASMs Placebo 100 48.1 12–75 24 ± 10
Pregabalin 50 mg/day 88 25 ± 11.8
Pregabalin 150 mg/day 86 24 ± 12.8
Pregabalin 300 mg/day 90 26.2 ± 13.5
Pregabalin 600 mg/day 89 25.5 ± 13.7
French 2010 20592253 Patients were included if they were aged 16–65 years with well-characterized focal epilepsy/epileptic syndrome (International League Against Epilepsy classification, 1989) 11 experiencing at least 4 partial-onset seizures during a 4-week prospective baseline period and taking 1 or 2 concomitant ASMs maintained at stable dose from at least 1 month before screening and throughout the study Placebo 54 24 (44.4) 33.6 (11.3) 21.7 (13.0)
Brivaracetam 5 mg/day 50 30 (60.0) 32.7 (12.2) 16.0 (11.5)
Brivaracetam 20 mg/day 52 28 (53.8) 35.3 (13.7) 22.9 (13.5)
Brivaracetam 50 mg/day 52 28 (53.8) 30.9 (11.6) 19.1 (10.8)
French 2014 24962242 Patients were ≥18 years. A minimum of six partial seizures with an observable component with no 28-day period free of partial seizures during the 8-week baseline was required for randomization Placebo 109 44.5 38.7 (18–72) NA
Pregabalin 165 mg/day 98 47 37.9 (18–70) NA
Pregabalin 330 mg/day 111 51.3 39.6 (18–75) NA
French 2016 27521437 Key criteria were age 18–80 years, a diagnosis of epilepsy with partial-onset seizures (equivalent to the 2010 ILAE classification1of focal seizures) that had been inadequately controlled with 2 to 5 prior ASMs, and receiving 1 or 2 standard ASMs (other than pregabalin or gabapentin) with a minimum of 4 partial-onset seizures Pregabalin 150, 300, 450, and 600 mg/day 241 127 (52.7) 34.9 (13.0) 19.8 (0.1–78.1)
Gabapentin 300, 600, 1,200, 1,500, and 1,800 mg/day 241 130 (53.9) 35.3 (12.9) 19.9 (0.0–62.1)
French 2021 34521687 Participants aged 18–75 years were eligible for enrolment if they had a clinical diagnosis of focal epilepsy (confirmed by an independent epilepsy review committee) and met the International League Against Epilepsy’s 2010 definition of drug resistance. In addition, participants must have experienced ≥6 seizures during the baseline period, with no more than 21 consecutive seizure-free days, and been on a stable regimen of 1–5 ASDs during the 4 weeks before the screening visit and throughout the baseline period Placebo 34 18 (53) 39.1 (12.17) 19.6 (14.69)
Natalizumab 300 mg/day 32 18 (56) 42.8 (14.56) 19.7 (13.30)
Gil-Nagel 2009 19832771 ≥18 years, assessed as being in general good health, other than epilepsy; diagnosed with simple or complex partial seizures (with or without secondary generalization) for a minimum of 12 months prior to screening; experienced at least four partial-onset seizures Placebo 87 44.8 ≧18 23.8 ± 13.03
Eslicarbazepine acetate 800 mg/day 85 22.5 ± 11.78
Eslicarbazepine acetate 1,200 mg/day 80 23.0 ± 13.01
Guberman 2002 12225311 18–65 years had at least three partial-onset seizures, with or without secondary generalization, within the 4-week baseline Placebo 91 50 36 (18–67) NA
Topiramate 200 mg/day 168 46 37 (18–64) NA
Hogan 2014 25461205 18–75 years with a confirmed diagnosis of partial-onset seizures (for ≥1 year) with a minimum of eight partial-onset seizures (with or without secondary generalization) and no more than 21 consecutive seizure-free days during the 8-week baseline phase Placebo 63 52.8 37.6 NA
Topiramate 200 mg/day 52 53.2 37.6 NA
Hong 2016 27669155 Patients aged between 16 and 70 years with uncontrolled partial-onset seizures, with or without secondary generalization (Commission on Classification and Terminology of the International League Against Epilepsy, 1981), were eligible for study enrollment if they were taking stable daily Placebo 184 102 (55.4) 31.8 (12.0) 16.8 (11.5)
Lacosamide 200 mg/day 183 94 (51.4) 33.2 (12.2) 18.3 (10.9)
Lacosamide 400 mg/day 180 104 (57.8) 32.3 (11.9) 17.9 (11.7)
Inoue 2021 34246118 Male and female aged 16–70 years who completed a double-blind trial Placebo 164 91 (55.5) 32.2 (12.2) 17.0 (11.6)
Lacosamide 200 mg/day 163 84 (51.5) 33.6 (12.5) 18.4 (10.8)
Lacosamide 400 mg/day 146 84 (57.5) 32.2 (11.4) 16.5 (10.7)
Kalviainen 1998 9551842 16–75 years, had a documented history of partial seizures (six in the previous 8 weeks) supported by one of the following findings: an interictal electroencephalogram (EEG) demonstrating a focal abnormality; an interictal EEG demonstrating unilateral or bilateral asynchronous activity; or evidence of a focal CNS lesion by computed tomography o magnetic resonance imaging Placebo 77 58.4 16–75 23.0 (1–49)
Tiagabine 30 mg/day 77 24.9 (2–52)
Klein 2015 26471380 Eligible patients were aged ≥16–80 years, with well characterized focal epilepsy or epileptic syndrome Placebo 261 51% 39.8 (12.5) 22.7 (13.3)
Brivaracetam 100 mg/day 253 40.3% 39.1 (13.4) 22.2 (13.3)
Brivaracetam 200 mg/day 250 53.2% 39.8 (12.8) 23.4 (14.6)
Krauss 2020 31734103 Eligible patients were adults aged 18–70 years with a diagnosis of focal epilepsy according to the International League Against Epilepsy’s Classification of Epileptic Seizures. The epilepsy had to be uncontrolled despite treatment with at least one anti-epileptic drug within the past 2 years. Patients must have been taking one to three concomitant ASM at stable doses for at least 4 weeks before screening Placebo 108 50.5 18–70 NA
Cenobamate 100 mg/day 108 NA
Cenobamate 200 mg/day 110 NA
Cenobamate 400 mg/day 111 NA
Lee 2009 19222545 ≥18 years patients were required to have tried at least one ASM at the maximally tolerable dose and had to be taking one to three ASMs at a clinically relevant dose. Additional inclusion criteria included a minimum of four seizures that had occurred over at least 2 days during a 6-week base line period with no 28-day seizure-free period Placebo 59 58 35.1 18 (0.7–48.1)
Pregabalin 150–600 mg/day 119 44 33.3 16.5 (0.3–48.0)
Lindberger 2000 11051124 Patients with partial epilepsy were eligible if they had tried no more than two ASM monotherapy regimens Gabapentin 2,400 and 3,600 mg/day 50 28 (56) 34.5 (13–68) 3.5 (0–36)
Vigabatrin 2,000 and 4,000 mg/day 52 23 (44) 33 (14–56) 9.5 (0–43)
Matsuo 1993 8232944 Patient population. Men or women, aged 18–65 years (inclusive), were eligible for the study if they demonstrated simple or complex partial seizures (with or without secondary generalization) that were refractory to treatment with up to three currently marketed ASMs Placebo 73 22 (30%) 34 (18–63) 21.5
Lamotrigine 300 mg/day 71 30 (42%) 33 (20–57) 22.4
Lamotrigine 500 mg/day 72 15 (12%) 32 (18–59) 21.8
Naritoku 2007 17938371 Patients more than 12 years old diagnosed with epilepsy with partial seizures and taking one to two baseline ASM were randomized to adjunctive once-daily lamotrigine or placebo in a double-blind, parallel-group trial Placebo 121 49.6 ≧12 22.1 ± 16.1
Lamotrigine 200/300/500 mg/day 118 21.8 ± 13.2
Nishida 2018 29250772 Eligible patients were aged ≥12 years; diagnosed with partial-onset seizures, with or without SG seizures, according to the 1981 International League Against Epilepsy Classification of Epileptic Seizures9; had uncontrolled partial-onset seizures, despite ≥2 ASMs within the last 2 years; ≥5 partial-onset seizures during baseline; and were taking stable doses of 1–3 approved concomitant ASMs. Only one ASM was permitted (carbamazepine, phenytoin, or oxcarbazepine) Placebo 175 86 (49.1) 34.5 (13.2) 17.5 (10.9)
Perampanel 4 mg/day 174 80 (46) 33.1 (13.2) 17.4 (11.1)
Perampanel 8 mg/day 175 91 (52) 33.6 (14.1) 16.9 (11.5)
Perampanel 12 mg/day 180 87 (48.3) 32.3 (12.3) 17.4 (11.2)
No authors listed 1993 8232945 ≥16 years, only patients with documented partial seizures refractory to treatment with currently available ASMs were enrolled in the study. To qualify, patients had to have had an average of at least four clearly recognizable partial seizures per month for the 3 months prior to baseline, while taking one or two ASMs at stable dosages Placebo 95 69 (70) 34 (17–66) 22 (2–49)
Gabapentin 600 mg/day 49 36 (68) 34 (16–67) 20 (3–36)
Gabapentin 1,200 mg/day 91 60 (59) 35 (19–65) 21 (3–45)
Gabapentin 1,800 mg/day 53 37 (69) 35 (18–70) 21 (1–41)
No authors listed 1990 1971862 Patients eligible for the study were those with at least 1 partial seizure per week, with or without secondary generalization, despite adequate medication with one or two standard anticonvulsants Placebo 66 41.7 14–73 17 (2–47)
Gabapentin 1,200 mg/day 61 19 (4–38)
Peltola 2009 19317886 12–70 years of, with recurrent partial-onset seizures despite receiving at least one but no more than three concomitant ASMs. Weigh ≥50 kg and have a confirmed diagnosis of partial-onset seizures, whether or not secondarily generalized, for at least 6 months preceding the screening visit and refractory to pharmacotherapy with one to three ASMs. During the 8-week baseline period, patients were required to have at least eight partial seizures, with or without secondary generalization, and at least two partial seizures in each 4-week inter Placebo 79 62.7 12–68 16.43 ± 11.93
Levetiracetam 1,000 mg/day 79 13.11 ± 10.87
Privitera 1996 8649569 18–65 years with a history of refractory partial epilepsy with or without secondary generalization were eligible for participation in the study Placebo 47 70.2 35.0 (18–68) NA
Topiramate 600 mg/day 48 79.2 35.6 (18–57) NA
Topiramate 800 mg/day 48 85.4 34.3 (18–67) NA
Topiramate 1,000 mg/day 47 85.1 36.3 (18–64) NA
Sackellares 2004 15144425 17–65 years patients had to be receiving at least one, but no more than two of the following ASMs, had a history of at least four complex partial seizures per month; and had no more than eight generalized tonics Placebo 74 58.1 36.4 (17.8–67.5) NA
Zonisamide 7 mg/kg/day 78 74.4 35.6 (17.9–64.1) NA
Schmidt 1993 8325280 18–59 years. During the 4 months preceding the baseline period all patients had an average of at least four complex partial seizures per month in spite of therapeutic plasma concentrations of standard ASM. The diagnosis of seizure types was based on the International Classification of Epileptic Seizures Placebo 68 139 18–59 23.5
Zonisamide 500 mg/day 71 20.9
Sharief 1996 8956919 18–65 years have an unequivocal history of partial seizures with or without secondarily generalized seizures. Those patients who had at least 8 partial seizures during an 8-week baseline period in which they were maintained at therapeutic plasma ASM concentrations were qualified to enter the double-blind treatment phase. Patients with a seizure-free interval that exceeded 3 weeks or with more than one seizure-free interval of 3 weeks during the baseline period were excluded Placebo 24 72.2 32.6 NA
Topiramate 400 mg/day 23 91.3 35.4 NA
Shorvon 2000 10999557 16–65 years patients were required to maintain stable dose regimens of a maximum of two ASMs for at least 4 weeks before the selection visit, as well as throughout the study. Patients had to have at least four partial seizures during each 4-week interval in the 8- or 12-week baseline period Placebo 112 49 37 (16–69) 23.2 ± 11.0
Levetiracetam 1,000 mg/day 106 48 36 (16–68) 23.8 ± 12.3
Levetiracetam 2,000 mg/day 106 48 37 (14–65) 23.6 ± 13.3
Tassinari 1996 8764816 18–65 years patients who met the requirements for inclusion during the screening phase were further evaluated during an 8-week baseline phase in which they were required to have at least eight partial seizures while being maintained at therapeutic plasma ASM concentrations Placebo 29 68 32.9 NA
Topiramate 600 mg/day 26 NA
Tsai 2006 16417534 16–60 years, all randomized patients had been diagnosed as having epilepsy for ≥6 months before the study. Partial seizures were treatment resistant in all cases, and, during an 8-week baseline period, all patients had at least four complex or secondarily generalized partial seizures Placebo 47 53.2 31.7 18.7 ± 10.7
Levetiracetam 2000 mg/day 47 36.2 32.8 18.6 ± 8.5
Uthman 1998 9443711 12–77 years, good health except for epilepsy; occurrence of at least 6 CPS alone or in combination with any other seizure type in the 8 weeks preceding the screening visit (with each of the two 4-week segments containing at least l CPS); electroencephalographic evidence of a unilateral or bilateral abnormality consistent with CPS; and availability of at least I neuroimaging study of the brain to rule out the presence of any progressive lesions Placebo 90 58 12–77 22.9 (1.4–65.8)
Tiagabine 16 mg/day 61
Tiagabine 32 mg/day 86
Tiagabine 56 mg/day 55
Wu 2009 18657175 16–70 years, patients had to present with treatment-resistant partial onset seizures to be eligible and had to have experienced at least eight partial-onset seizures during the 8-week historical baseline period Placebo 100 54 32.8 (16–64) 17.3 ± 12.1
Levetiracetam 1,000–3,000 mg/day 102 50 32.7 (15–70) 16.5 ± 12.7
Xiao 2009 19176965 16–70 years were invalid to current anti-epileptic therapy and had experienced at least 4 seizures per month (averaged over the preceding 2 months, despite therapy with other marketed ASMs) Placebo 28 42.9 32.5 (18–58) 16.1 ± 12.5
Levetiracetam 3,000 mg/day 28 42.9 32.8 (17–60) 14.1 ± 9.4
Yamauchi 2006 16884455 ≥16 years, with partial seizures as defined by criteria developed by the International League Against Epilepsy. Weighing 40–110 kg, were eligible if they were on a stable dose of no more than two ASM. Placebo 82 48.3 ≧16 19.5 (2.1–47.0)
Gabapentin 1,200 mg/day 86 19.8 (4.0–42.0)
Gabapentin 1800 mg/day 41 21.2 (5.2–43.3)
Yen 2000 10999555 18–65 years of age with a history of partial seizures that had not responded to adequate doses of ASM treatment for 2 or more years Placebo 23 56.5 32.0 (22–48) 18.9 ± 11.1
Topiramate 300 mg/day 23 26.1 31.4 (18–54) 14.9 ± 10.9
Zaccara 2014 24902473 Patients were aged ≥18 years, with a diagnosis of epilepsy with partial seizures (equivalent to focal seizures in the 2010 ILAE classification), which were historically inadequately controlled with at least 2, but no more than 5, prior ASMs Pregabalin150, 300, 450 and 600 mg/day 254 120 (47.2) 32.7 ± 11.2 15.5 (2.0–52.8
Levetiracetam 1,000, 2000 and 3,000 mg/day 255 125 (49.0) 36.3 ± 12.2 17.3 (1.9–59.6)
Zhou 2008 18024209 16–70 years, whose partial-onset seizures (simple or complex partial with or without secondary generation, according to the International League Against Epilepsy classification) were poorly controlled by at least one first-line ASM at the time of the study. Poor control was defined as having a minimum of eight seizures during the 8-week baseline period with a minimum of two seizures during each 4-week period Placebo 11 54.1 16–70 16.5 ± 7.2
Levetiracetam 3,000 mg/day 13 8.7 ± 6.4

Note: ASMs: Anti-seizure medications; CNS: central nervous system; CP: complex partial; CPS: complex partial seizures; CT: computed tomography; EEG: electroencephalo-graph; ILAE: International League Against Epilepsy; MRI: magnetic resonance imaging; NA: no reported; SGS: secondary generalization; SP: simple partial; VNS: vagus nerve stimulation.

 Effective outcome 50% Response rate

The pool of 46 RCTs (Gabapentin in Partial Epilepsy, 1990; Anhut et al., 1994; The US Gabapentin Study Group No. 5, 1993; Schmidt et al., 1993; French et al., 1996; Privitera et al., 1996; Faught et al., 1996; Tassinari et al., 1996; Sharief et al., 1996; Faught, 1997; Ben-Menachem, 1997; Uthman et al., 1998; Bruni et al., 2000; Cereghino et al., 2000; Yen et al., 2000; Shorvon et al., 2000; Lindberger et al., 2000; Barcs et al., 2000; French et al., 2003; Arroyo et al., 2004; Sackellares et al., 2004; Brodie, 2004; Brodie et al., 2005; Beydoun et al., 2005; Tsai et al., 2006; Yamauchi et al., 2006; Naritoku et al., 2007; Zhou et al., 2008; Wu et al., 2009; Xiao et al., 2009; Lee et al., 2009; Gil-Nagel et al., 2009; Ben-Menachem et al., 2010; French et al., 2010; Biton et al., 2011; Zaccara et al., 2014; French et al., 2014; Hogan et al., 2014; Klein et al., 2015; French et al., 2016; Hong et al., 2016; Nishida et al., 2018; Krauss et al., 2020; Chung et al., 2020; French et al., 2021; Baulac et al., 2010), including 12,120 study participants, contributed to the analysis of the 50% response rate. Figure 2 illustrated a network plot of 50% response rate assessment of 16 eligible ASMs as adjunctive therapy and placebo for the treatment of drug-resistant focal epilepsy.

Network plot for 50% response rate.

As shown in Table 2, the consequence of direct comparisons showed that the following ASMs as adjunctive therapy, including brivaracetam, cenobamate, eslicarbazepine acetate, gabapentin, lacosamide, levetiracetam, oxcarbazepine, perampanel, pregabalin, rufinamide, tiagabine, topiramate, vigabatrin and zonisamide, demonstrated statistically significant in 50% response rate than that of placebo. Nevertheless, the other results were no statistically significant differences.

Results of network and traditional paired meta-analysis for 50% response rate.

Placebo 2.07 (1.53, 2.81) 2.12 (1.56, 2.88) 1.95 (1.41, 2.70) 2.30 (1.76, 3.02) 2.22 (1.47, 3.35) 1.55 (1.00, 2.40) 2.43 (1.88, 3.15) 1.77 (0.65, 4.86) 3.03 (2.08, 4.40) 1.72 (1.21, 2.44) 2.06 (1.70, 2.50) 2.28 (1.20, 4.31) 4.07 (2.03, 8.18) 3.10 (2.44, 3.95) 2.34 (1.58, 3.46) 2.40 (1.76, 3.27)
1.94 (1.60, 2.36) Brivaracetam 1.02 (0.67, 1.58) 0.94 (0.60, 1.47) 1.11 (0.74, 1.67) 1.07 (0.64, 1.79) 0.75 (0.44, 1.28) 1.18 (0.79, 1.75) 0.86 (0.30, 2.45) 1.46 (0.90, 2.37) 0.83 (0.52, 1.32) 0.99 (0.70, 1.42) 1.10 (0.54, 2.23) 1.97 (0.92, 4.21) 1.50 (1.02, 2.21) 1.13 (0.69, 1.85) 1.16 (0.75, 1.79)
2.14 (1.76, 2.59) / Cenobamate 0.92 (0.59, 1.44) 1.09 (0.72, 1.63) 1.04 (0.62, 1.75) 0.73 (0.43, 1.25) 1.15 (0.77, 1.71) 0.83 (0.29, 2.40) 1.43 (0.88, 2.31) 0.81 (0.51, 1.29) 0.97 (0.67, 1.39) 1.07 (0.53, 2.18) 1.92 (0.90, 4.11) 1.46 (0.99, 2.16) 1.10 (0.67, 1.81) 1.13 (0.73, 1.75)
1.95 (1.41, 2.71) / / Eslicarbazepine acetate 1.18 (0.77, 1.80) 1.14 (0.67, 1.92) 0.80 (0.46, 1.37) 1.25 (0.82, 1.89) 0.91 (0.31, 2.62) 1.55 (0.95, 2.54) 0.88 (0.55, 1.42) 1.05 (0.72, 1.54) 1.17 (0.57, 2.39) 2.09 (0.97, 4.50) 1.59 (1.06, 2.38) 1.20 (0.72, 1.99) 1.23 (0.78, 1.92)
2.52 (1.89, 3.37) / / / Gabapentin 0.96 (0.59, 1.58) 0.67 (0.40, 1.13) 1.06 (0.73, 1.52) 0.77 (0.27, 2.19) 1.31 (0.83, 2.08) 0.75 (0.48, 1.16) 0.89 (0.66, 1.20) 0.99 (0.49, 1.98) 1.77 (0.84, 3.74) 1.35 (0.94, 1.93) 1.02 (0.68, 1.52) 1.04 (0.69, 1.57)
2.22 (1.75, 2.83) / / / / Lacosamide 0.70 (0.38, 1.28) 1.10 (0.67, 1.79) 0.80 (0.27, 2.38) 1.37 (0.78, 2.38) 0.78 (0.45, 1.33) 0.93 (0.59, 1.47) 1.03 (0.48, 2.20) 1.84 (0.82, 4.13) 1.40 (0.87, 2.26) 1.06 (0.60, 1.86) 1.08 (0.65, 1.81)
1.54 (0.86, 2.74) / / / / / Lamotrigine 1.57 (0.94, 2.60) 1.14 (0.38, 3.42) 1.95 (1.10, 3.46) 1.11 (0.64, 1.94) 1.33 (0.82, 2.14) 1.47 (0.68, 3.18) 2.62 (1.15, 5.97) 2.00 (1.21, 3.29) 1.51 (0.84, 2.70) 1.54 (0.91, 2.63)
2.57 (1.93, 3.42) / / / / / / Levetiracetam 0.73 (0.26, 2.06) 1.24 (0.79, 1.96) 0.71 (0.46, 1.09) 0.85 (0.63, 1.13) 0.94 (0.47, 1.86) 1.67 (0.80, 3.52) 1.28 (0.90, 1.81) 0.96 (0.60, 1.53) 0.99 (0.66, 1.48)
1.77 (0.73, 4.31) / / / / / / / Natalizumab 1.71 (0.58, 5.01) 0.97 (0.33, 2.83) 1.16 (0.42, 3.25) 1.28 (0.39, 4.24) 2.30 (0.67, 7.84) 1.75 (0.62, 4.95) 1.32 (0.45, 3.90) 1.35 (0.47, 3.89)
3.03 (2.13, 4.32) / / / / / / / / 0xcarbazepine 0.57 (0.34, 0.95) 0.68 (0.45, 1.04) 0.75 (0.36, 1.58) 1.35 (0.61, 2.97) 1.03 (0.66, 1.60) 0.77 (0.45, 1.33) 0.79 (0.49, 1.29)
1.72 (1.21, 2.46) / / / / / / / / / Perampanel 1.20 (0.80, 1.78) 1.32 (0.64, 2.74) 2.37 (1.08, 5.16) 1.80 (1.18, 2.75) 1.36 (0.81, 2.29) 1.39 (0.87, 2.22)
2.10 (1.51, 2.94) / / / 0.96 (0.82, 1.12) / / 1.007 (0.84, 1.20) / / / Pregabalin 1.11 (0.57, 2.16) 1.98 (0.96, 4.08) 1.51 (1.11, 2.05) 1.14 (0.74, 1.74) 1.16 (0.81, 1.68)
2.28 (1.49, 3.48) / / / / / / / / / / / Rufinamide 1.79 (0.69, 4.61) 1.36 (0.69, 2.70) 1.03 (0.49, 2.18) 1.05 (0.52, 2.14)
4.08 (2.05, 8.12) / / / / / / / / / / / / Tiagabine 0.76 (0.36, 1.59) 0.57 (0.26, 1.28) 0.59 (0.27, 1.26)
2.99 (2.43, 3.68) / / / / / / / / / / / / / Topiramate 0.75 (0.48, 1.19) 0.77 (0.52, 1.14)
2.07 (1.45, 2.95) / / / 1.21 (0.88, 1.67) / / / / / / / / / / Vigabatrin 1.02 (0.62, 1.69)
2.43 (1.93, 3.06) / / / / / / / / / / / / / / / Zonisamide

Note: Comparisons between anti-seizure medications should be read from right to left, and the results are all comparisons between treatments defined on the bottom right and treatments defined on the top left. The table is divided into lower left and upper right sections with anti-seizure medications as the dividing line. The upper right represents the network comparison results, and the lower left part represents the direct comparison results. For comparison results, when relative risk (RR) < 1, tended to define treatment on the left, when RR > 1, treatment tends to be defined to the right. Significant results are in bold and underline, and “/” means that the results are not available.

Compared with placebo in the network meta-analysis, ASMs as adjunctive therapy, including brivaracetam, cenobamate, eslicarbazepine acetate, gabapentin, lacosamide, lamotrigine, levetiracetam, oxcarbazepine, perampanel, pregabalin, rufinamide, tiagabine, topiramate, vigabatrin, and zonisamide, demonstrated statistically significant in 50% response rate, as detailed in Table 2. The results of other ASMs as adjunctive therapy were shown in Table 2.

The ASMs as adjunctive therapy were assessed and graded based on the SUCRA, with tiagabine (92.7%) demonstrating the most optimal therapeutic outcome, subsequent to topiramate (87.3%), oxcarbazepine (83%) and levetiracetam (62.8%). The three ASMs as adjunctive therapy with the worst therapeutic effects were placebo (1.1%), lamotrigine (17.8%) and perampanel (24.7%) in Figure 3.

Ranking for all outcomes.

 Safety outcomes Dizziness

A total of 45 studies (Gabapentin in Partial Epilepsy, 1990; Anhut et al., 1994; The US Gabapentin Study Group No. 5, 1993; Schmidt et al., 1993; Privitera et al., 1996; Faught et al., 1996; Tassinari et al., 1996; Uthman et al., 1998; Bruni et al., 2000; Cereghino et al., 2000; Yen et al., 2000; Shorvon et al., 2000; Barcs et al., 2000; French et al., 2003; Arroyo et al., 2004; Brodie, 2004; Brodie et al., 2005; Beydoun et al., 2005; Tsai et al., 2006; Yamauchi et al., 2006; Naritoku et al., 2007; Wu et al., 2009; Xiao et al., 2009; Lee et al., 2009; Gil-Nagel et al., 2009; Ben-Menachem et al., 2010; French et al., 2010; Biton et al., 2011; Zaccara et al., 2014; French et al., 2014; Klein et al., 2015; French et al., 2016; Hong et al., 2016; Nishida et al., 2018; Krauss et al., 2020; Chung et al., 2020; French et al., 2021; Baulac et al., 2010; Matsuo et al., 1993; Ben-Menachem et al., 1996; Kälviäinen et al., 1998; Chadwick et al., 2000; Guberman et al., 2002; Peltola et al., 2009; Inoue et al., 2021) comprising 12,608 participants contributed to the analysis of the safety outcome of dizziness. Supplementary Figure S1 illustrated a network plot of the safety outcomes dizziness assessment of 17 eligible ASMs as adjunctive therapy and placebo for the treatment of drug-resistant focal epilepsy.

As shown in Supplementary Table S2, the consequence of direct comparisons showed that, compared with placebo, the following ASMs as adjunctive therapy demonstrated statistically significant in dizziness: cenobamate, eslicarbazepine acetate, gabapentin, levetiracetam, oxcarbazepine, perampanel, pregabalin, remacemid, rufinamide, tiagabine, topiramate and zonisamide. Nevertheless, the other results were no statistically significant differences.

The findings of the network meta-analysis indicated that, compared with placebo, ASMs as adjunctive therapy, including brivaracetam, cenobamate, eslicarbazepine acetate, gabapentin, lamotrigine, levetiracetam, oxcarbazepine, perampanel, pregabalin, remacemid, rufinamide, tiagabine, topiramate and zonisamide, demonstrated statistically significant in dizziness (Supplementary Table S2). The results of other ASMs as adjunctive therapy were shown in Supplementary Table S2.

According to the SUCRA, all ASMs as adjunctive therapy assessed for the safety outcome of dizziness were rated, with placebo (97.8%) exhibiting the best therapeutic benefit, subsequently followed by lacosamide (86.3%), cenobamate (74.5%) and lamotrigine (73.4%). The three ASMs as adjunctive therapy with the worst therapeutic effects were perampanel (5.8%), natalizumab (20.3%) and zonisamide (23.6%) (Figure 3).

 Somnolence

A total of 42 studies (Gabapentin in Partial Epilepsy, 1990; Anhut et al., 1994; The US Gabapentin Study Group No. 5, 1993; Schmidt et al., 1993; Privitera et al., 1996; Faught et al., 1996; Tassinari et al., 1996; Sharief et al., 1996; Cereghino et al., 2000; Shorvon et al., 2000; Barcs et al., 2000; French et al., 2003; Arroyo et al., 2004; Brodie, 2004; Brodie et al., 2005; Beydoun et al., 2005; Tsai et al., 2006; Yamauchi et al., 2006; Naritoku et al., 2007; Wu et al., 2009; Xiao et al., 2009; Lee et al., 2009; Gil-Nagel et al., 2009; Ben-Menachem et al., 2010; French et al., 2010; Biton et al., 2011; Zaccara et al., 2014; French et al., 2014; Klein et al., 2015; French et al., 2016; Hong et al., 2016; Nishida et al., 2018; Krauss et al., 2020; Chung et al., 2020; French et al., 2021; Baulac et al., 2010; Matsuo et al., 1993; Kälviäinen et al., 1998; Chadwick et al., 2000; Guberman et al., 2002; Peltola et al., 2009; Inoue et al., 2021) encompassing 12,163 participants contributed to the analysis of the safety outcome of somnolence. Supplementary Figure S2 illustrated a network plot of safety outcomes somnolence assessment of 16 eligible ASMs as adjunctive therapy and placebo for the treatment of drug-resistant focal epilepsy.

In the results of direct comparisons, compared with placebo, ASMs as adjunctive therapy including cenobamate, gabapentin, levetiracetam, oxcarbazepine, pregabalin, topiramate and zonisamide demonstrated statistically significant in somnolence (Supplementary Table S3). Nevertheless, the other results were no statistically significant differences.

The findings of the network meta-analysis indicated that, compared with placebo, ASMs as adjunctive therapy, including brivaracetam, cenobamate, gabapentin, levetiracetam, oxcarbazepine, pregabalin, topiramate and zonisamide, demonstrated statistically significant in somnolence (Supplementary Table S3). The results of other ASMs as adjunctive therapy were shown in Supplementary Table S3.

The ASMs as adjunctive therapy were ranked based on the SUCRA and the results indicate that natalizumab (93.3%) exhibited the most favourable therapeutic effect, subsequent to remacemide (85.1%), placebo (82.7%) and tiagabine (79.1%). The three ASMs as adjunctive therapy with the worst therapeutic effects were cenobamate (10%), zonisamide (12.7%) and topiramate (18.2%) in Figure 3.

 Headache

A total of 38 studies (Anhut et al., 1994; The US Gabapentin Study Group No. 5, 1993; Privitera et al., 1996; Faught et al., 1996; Tassinari et al., 1996; Sharief et al., 1996; Bruni et al., 2000; Cereghino et al., 2000; Yen et al., 2000; Shorvon et al., 2000; Barcs et al., 2000; French et al., 2003; Arroyo et al., 2004; Brodie et al., 2005; Tsai et al., 2006; Yamauchi et al., 2006; Naritoku et al., 2007; Wu et al., 2009; Lee et al., 2009; Gil-Nagel et al., 2009; Ben-Menachem et al., 2010; French et al., 2010; Biton et al., 2011; Zaccara et al., 2014; Klein et al., 2015; French et al., 2016; Hong et al., 2016; Nishida et al., 2018; Krauss et al., 2020; Chung et al., 2020; French et al., 2021; Baulac et al., 2010; Matsuo et al., 1993; Ben-Menachem et al., 1996; Kälviäinen et al., 1998; Chadwick et al., 2000; Peltola et al., 2009; Inoue et al., 2021) encompassing 11,011 participants contributed to the analysis of the headache safety outcome. Supplementary Figure S3 illustrated a network plot of the safety outcomes headache assessment of 17 eligible ASMs as adjunctive therapy and placebo for the treatment of drug-resistant focal epilepsy.

In the results of direct comparisons, compared with placebo, ASMs as adjunctive therapy including pregabalin, demonstrated statistically significant in headache (Supplementary Table S4). Nevertheless, the other results were no statistically significant differences.

The findings of the network meta-analysis indicated that, compared with placebo, ASMs as adjunctive therapy, including pregabalin, demonstrated statistically significant in headache (Supplementary Table S4). The results of other ASMs as adjunctive therapy were shown in Supplementary Table S4.

The ASMs as adjunctive therapy were ranked based on the SUCRA, with pregabalin (91.7%) showing the best therapeutic effect, subsequent to zonisamide (89.7%), brivaracetam (75.4%) and topiramate (69%). The three ASMs as adjunctive therapy exhibiting the most unfavorable therapeutic effects were cenobamate (16.9%), vigabatrin (22.7%) and eslicarbazepine acetate (26.6%) in Figure 3.

 Ataxia

12 studies (Anhut et al., 1994; The US Gabapentin Study Group No. 5, 1993; Faught et al., 1996; Bruni et al., 2000; Barcs et al., 2000; French et al., 2003; Brodie, 2004; Beydoun et al., 2005; Krauss et al., 2020; Baulac et al., 2010; Matsuo et al., 1993; Chadwick et al., 2000) encompassing 3,596 study participants contributed to the analysis of the safety outcome of ataxia. Supplementary Figure S4 illustrated a network plot of safety outcomes ataxia assessment of 9 eligible ASMs as adjunctive therapy and placebo for the treatment of drug-resistant focal epilepsy.

In the results of direct comparisons, compared with placebo, ASMs as adjunctive therapy including cenobamate, gabapentin, oxcarbazepine, pregabalin, topiramate, zonisamide, demonstrated statistically significant in ataxia (Supplementary Table S5). Nevertheless, the other results were no statistically significant differences.

The findings of the network meta-analysis indicated that, compared with placebo, ASMs as adjunctive therapy, including cenobamate, gabapentin, lamotrigine, oxcarbazepine, pregabalin, topiramate, zonisamide, demonstrated statistically significant in ataxia (Supplementary Table S5). The results of other ASMs as adjunctive therapy were shown in Supplementary Table S5.

The ASMs as adjunctive therapy were ranked based on the SUCRA, with the placebo (97.7%) demonstrating optimal therapeutic effectiveness, subsequent to gabapentin (77%) and lamotrigine (68.5%). The three ASMs as adjunctive therapy with the worst therapeutic effects were zonisamide (14.6%), vigabatrin (28.9%) and remacemide (34.7%) in Figure 3.

 Diplopia

The safety outcome study of diplopia included 16 studies (Anhut et al., 1994; The US Gabapentin Study Group No. 5, 1993; Privitera et al., 1996; Faught et al., 1996; Bruni et al., 2000; Barcs et al., 2000; Arroyo et al., 2004; Beydoun et al., 2005; Yamauchi et al., 2006; Gil-Nagel et al., 2009; Ben-Menachem et al., 2010; Krauss et al., 2020; Baulac et al., 2010; Matsuo et al., 1993; Kälviäinen et al., 1998; Chadwick et al., 2000) with 4,487 participants. Supplementary Figure S5 illustrated a network plot of the safety outcomes diplopia assessment of 10 eligible ASMs as adjunctive therapy and placebo for the treatment of drug-resistant focal epilepsy.

In the results of direct comparisons, compared with placebo, ASMs as adjunctive therapy including oxcarbazepine cenobamate, eslicarbazepine acetate, gabapentin, lamotrigine, oxcarbazepine, pregabalin and topiramate, demonstrated statistically significant in diplopia (Supplementary Table S6). Nevertheless, the other results were no statistically significant differences.

The findings of the network meta-analysis indicated that, compared with placebo, ASMs as adjunctive therapy, including cenobamate, eslicarbazepine acetate, gabapentin, lamotrigine, oxcarbazepine, pregabalin and topiramate, demonstrated statistically significant in diplopia (Supplementary Table S6). The results of other ASMs as adjunctive therapy were shown in Supplementary Table S6.

The ASMs as adjunctive therapy were ranked based on the SUCRA, with the placebo (93%) demonstrating optimal therapeutic effectiveness, subsequent to topiramate (84.5%) and gabapentin (65.8%). The three ASMs as adjunctive therapy with the worst therapeutic effects were oxcarbazepine (10.9%), cenobamate (12.8%) and lamotrigine (19%) in Figure 3.

 Fatigue

A total of 22 studies (Anhut et al., 1994; The US Gabapentin Study Group No. 5, 1993; Schmidt et al., 1993; Privitera et al., 1996; Faught et al., 1996; Tassinari et al., 1996; Sharief et al., 1996; Bruni et al., 2000; Barcs et al., 2000; Brodie, 2004; Lee et al., 2009; Ben-Menachem et al., 2010; French et al., 2010; French et al., 2014; Klein et al., 2015; Nishida et al., 2018; Krauss et al., 2020; Chung et al., 2020; French et al., 2021; Ben-Menachem et al., 1996; Chadwick et al., 2000; Guberman et al., 2002) comprising 5,800 participants contributed to the analysis of the safety outcome of fatigue. Supplementary Figure S6 illustrated a network plot of the safety outcomes fatigue assessment of 12 eligible ASMs as adjunctive therapy and placebo for the treatment of drug-resistant focal epilepsy.

In the results of direct comparisons, compared with placebo, ASMs as adjunctive therapy including brivaracetam, cenobamate, gabapentin, oxcarbazepine, topiramate and zonisamide, demonstrated statistically significant in fatigue (Supplementary Table S7). Nevertheless, the other results were no statistically significant differences.

The findings of the network meta-analysis indicated that, compared with placebo, ASMs as adjunctive therapy, including brivaracetam, cenobamate, gabapentin, oxcarbazepine, topiramate, and zonisamide, demonstrated statistically significant in fatigue (Supplementary Table S7). The results of other ASMs as adjunctive therapy were shown in Supplementary Table S7.

The ASMs as adjunctive therapy were ranked based on the SUCRA, with the placebo (86.5%) demonstrating optimal therapeutic effectiveness, subsequent to natalizumab (81%) and eslicarbazepine acetate (77.6%). The three ASMs as adjunctive therapy with the worst therapeutic effects were pregabalin (23.2%), brivaracetam (31.9%) and cenobamate (34.4%), in Figure 3.

 Nausea

A total of 21 studies (Anhut et al., 1994; Schmidt et al., 1993; Tassinari et al., 1996; Yen et al., 2000; Shorvon et al., 2000; Barcs et al., 2000; Brodie et al., 2005; Yamauchi et al., 2006; Naritoku et al., 2007; Gil-Nagel et al., 2009; Ben-Menachem et al., 2010; Zaccara et al., 2014; French et al., 2014; Nishida et al., 2018; Krauss et al., 2020; Chung et al., 2020; French et al., 2021; Matsuo et al., 1993; Kälviäinen et al., 1998; Peltola et al., 2009; Inoue et al., 2021) encompassing 6,235 participants contributed to the safety outcome of nausea. Supplementary Figure S7 illustrated a network plot of the safety outcomes nausea assessment of 13 eligible ASMs as adjunctive therapy and placebo for the treatment of drug-resistant focal epilepsy.

In the results of direct comparisons, compared with placebo, ASMs as adjunctive therapy, including lamotrigine and oxcarbazepine demonstrated statistically significant in nausea (Supplementary Table S8). Nevertheless, the other results were no statistically significant differences.

The findings of the network meta-analysis indicated that, compared with placebo, ASMs as adjunctive therapy, cenobamate, eslicarbazepine acetate, lamotrigine and oxcarbazepine demonstrated statistically significant in nausea (Supplementary Table S8). In addition, except for a limited number of combination comparisons between active ASMs as adjunctive therapy and placebo, no statistically significant differences were found for the remaining comparisons between active ASMs as adjunctive therapy and placebo in Supplementary Table S8. The results of other ASMs as adjunctive therapy were shown in Supplementary Table S8.

The ASMs as adjunctive therapy were ranked based on the SUCRA, with pregabalin (87.6%) demonstrating optimal therapeutic effectiveness, subsequent to lacosamide (84.5%) and gabapentin (81.3%). The three ASMs as adjunctive therapy exhibiting the worst therapeutic outcomes were eslicarbazepine acetate (14.1%), cenobamate (15.8%) and oxcarbazepine (20.1%) in Figure 3.

 Test of inconsistency

Since closed loops were not formed for the outcomes of ataxia, fatigue, and diplopia, it was not possible to assess the inconsistency of these loops. Additionally, closed-loop structures were identified for the outcomes of a 50% response rate and adverse events (including dizziness, somnolence, headache, and nausea), and rigorous loop-consistency evaluation revealed no detectable inconsistencies within these loops.

 Publication bias

No publication bias were revealed in the network funnel plot of all outcomes (Supplementary Figures S8–S15).

 Discussion

While ASMs as adjunctive therapy remained the primary approach for managing epilepsy, some drugs inevitably caused varying degrees of harm to patients. Therefore, physicians must meticulously select specific drugs for treating epilepsy (Iyer and Marson, 2014). The study conducted an evidence-based assessment of comparative effectiveness and safety of ASMs as adjunctive therapy in drug-resistant focal epilepsy. The pertinent findings were as follows: tiagabine, topiramate, zonisamide, levetiracetam, rufinamide, and oxcarbazepine were more effective in controlling seizure frequency (as assessed by seizure-free analysis), whereas lacosamide was less effective than all other ASMs when used as adjunctive therapy.

Tiagabine was mechanistically one of the most precise ASMs in clinical use, but its use was limited to adjunctive therapy for partial seizures with or without secondary generalization in adolescents and adults (Mengel, 1994). Studies had demonstrated that adding tiagabine can reduce the frequency of seizures in individuals with drug-resistant focal seizures (Bresnahan et al., 2019). Another study found that, in the study population, short-term treatment with tiagabine at low doses had no cognitive or electroencephalogram adverse effects compared to placebo. Furthermore, tiagabine therapy did not result in worsening of cognitive function when used at high doses during long-term follow-up (Kälviäinen et al., 1996). Similarly, this study confirmed the substantial superiority of tiagabine in terms of therapeutic effectiveness.

Notably, in this study, topiramate achieved a high ranking for this outcome in 50% response rate (SUCRA: 87.3%), suggesting it may be a favorable first-choice option for this particular outcome. Furthermore, despite the risk of adverse events, such as dizziness, headache, ataxia, and diplopia, topiramate, demonstrated the highest safety profile and the lowest incidence of these events. One study found that when used in the management of drug-resistant focal epilepsy, topiramate could reduce the intensity and frequency of seizures while promoting overall stability, making it an effective, safe, and well-tolerated option for controlling disease progression (Viteva and Zahariev, 2020).

In the current study, levetiracetam exhibited an effective of 50% response rate and a relatively low risk profile (Marson et al., 2021). One study indicated that patients treated with levetiracetam were more prone to experiencing nausea (Zhao et al., 2017). Although levetiracetam lacked approval from the Food and Drug Administration (FDA) as a standalone treatment, it had been frequently used as a first-line ASM in the United States for both focal and generalized tonic-clonic seizures, and as an initial monotherapy in Europe (Abou-Khalil, 2019). Levetiracetam had minimal drug interactions and can be considered as the drug of choice for elderly individuals and fertile women (Sen et al., 2024). However, the findings also revealed that severe psychiatric symptoms, such as anger, violence, and even suicidal thoughts, may occur with levetiracetam administration. In most cases, these mental symptoms can be alleviated or disappear after reducing the dose or discontinuing the drug, but some patients may experience severe mental conditions that negatively impact their quality of life (Tao et al., 2024).

Gabapentin had proven effective as an adjunctive treatment for individuals with drug-resistant focal epilepsy and was generally well-tolerated. However, its used during pregnancy may pose risks to fetal neurodevelopment and congenital malformations (Honybun et al., 2024; Christensen et al., 2024). Some studies (Nakajima-Ohyama et al., 2024) had suggested that gabapentin can improve delirium and serve as a safe alternative therapy, but dose adjustments may be necessary to prevent sleepiness. It is important to note that gabapentin was associated with a higher incidence of dizziness, fatigue, and somnolence compared to placebo (Panebianco et al., 2021), and clinicians and patients should be vigilant of these symptoms during its use.

Pregabalin had demonstrated significant effectiveness in reducing the frequency of seizures in adults with drug-resistant focal epilepsy, but it also carried adverse reactions such as ataxia, dizziness, nausea, and weight gain (Panebianco et al., 2022). When combined with zonisamide, pregabalin had achieved impressive and sustained seizure control in patients with drug-resistant focal epilepsy, with minimal complications and fully reversible effects (Taghdiri et al., 2015).

Oxcarbazepine was an oral medication utilized for the treatment of focal-onset epilepsy, serving both as a monotherapy and an adjunctive therapy (Beydoun et al., 2020). Notably, other studies had indicated that oxcarbazepine exhibited superior overall effectiveness and was associated with fewer adverse events, such as vomiting, compared to other treatments (Zhang et al., 2022). However, it was crucial to acknowledge that our study included relatively small sample sizes for each drug, which may have introduced potential biases in the results. Consequently, further research was required to comprehensively evaluate the effectiveness and safety of oxcarbazepine.

Zonisamide, due to its adverse effects, was unlikely to emerge as the first-line treatment for focal epilepsy (Reimers and Ljung, 2019). Among other treatment options, brivaracetam, considered the second generation of levetiracetam, was a new ASM (Verrotti et al., 2021) that demonstrated high tolerability and effectiveness, particularly for adults with drug-resistant focal epilepsy (Bresnahan et al., 2022). Nevertheless, contrary to preclinical studies suggesting brivaracetam’s potential as an ideal treatment for focal epilepsy (Russo et al., 2017), this study found that the ASM was less effective in practical applications.

Monotherapy was widely accepted as the conventional primary treatment approach for epilepsy. However, when the initial administration of ASMs as adjunctive therapy proved ineffective, the option of employing combination therapy was contemplated. In cases where monotherapy was not controlled, the combination of lamotrigine and levetiracetam was considered. This combination regimen had the highest rate of seizure freedom both before and during pregnancy. Although the effectiveness of either ASM as adjunctive therapy alone may have been similar to that of sodium valproate in the treatment of generalized epilepsy, combination therapy with multiple agents was believed to have better effectiveness (Cohen et al., 2024). For patients who failed to respond to dual therapy, the prognosis could be improved through the reasonable selection of triple therapy, with about 15% of patients with refractory focal epilepsy achieving seizure-free status under triple therapy (Cai et al., 2024).

As indicated in clinical guidelines (Kanner et al., 2018), the following medications were effective in reducing the frequency of treatment-resistant adult focal epilepsy (Level A): immediate-release pregabalin, perampanel, and vigabatrin (though vigabatrin was not considered a first-line treatment). Medications that could reduce the frequency of treatment-resistant adult focal epilepsy (Level B) included lacosamide, eslicarbazepine, extended-release topiramate, and levetiracetam (used as add-on therapy for treatment-resistant childhood focal epilepsy). Perampanel and vigabatrin were found to be effective as add-on treatments for intractable focal epilepsy in adults, whereas oxcarbazepine required a high dose and its efficacy was dose-dependent. The drugs recommended in this study differed from those in the guidelines for several reasons. Firstly, the overall population studied varied, including differences in age and the severity of epilepsy. Secondly, the underlying anti-epileptic medication regimen was unclear. Thirdly, there may have been variations in the amount of adjuvant therapy used across different studies. Fourthly, the quality of research evidence varied across studies. Finally, the small sample size may have affected the accuracy of the results. By expanding the discussion of clinical implications, this study provides a broader and more specific analysis of controversial drugs from previous meta-analyses, making our findings more actionable and relevant to clinicians and patients. This will help ensure that our study has a meaningful impact on the management of drug-refractory focal epilepsy and ultimately improves patient outcomes.

This study had several limitations. Firstly, it lacked sufficient data and subgroup analyses regarding the ethnicity and comorbidities of the participants, which could have substantially impacted the overall conclusion. Secondly, the route of administration may have influenced the potential for side effects associated with each medication, dose, and treatment duration, potentially leading to significant differences among the studies included. Thirdly, we did not evaluate the etiology of drug resistance in drug-resistant focal epilepsy. Fourthly, patient heterogeneity, such as age and comorbidities, was not discussed, which could affect the generalizability of the findings. Fifthly, because some confounding factors were not mentioned in the original studies, subgroup analyses could not be performed. Finally, due to the lack of other safety data, some adverse event outcomes were excluded from the study for comparison, resulting in incomplete conclusions regarding safety.

 Conclusion

This network meta-analysis provided an overview of the 50% response rate and tolerability of the ASMs used in drug-resistant focal seizures, aiming to offer more authoritative and effective guidance for clinical medication guidelines. The analysis demonstrated that topiramate, tiagabine, oxcarbazepine, and levetiracetam were the four most effective adjuvant treatments for ASMs. However, it was important to note that topiramate and oxcarbazepine were associated with a higher risk of somnolence. Furthermore, there was a lack of comprehensive safety data for tiagabine and levetiracetam, necessitating further research in this area. Larger sample studies were still needed to strengthen the support for these findings and to gain a better understanding of the safety profiles of all the ASMs involved.

 Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding authors.

 Author contributions

N-JD: Conceptualization, Data curation, Formal Analysis, Investigation, Methodology, Project administration, Validation, Writing – original draft, Writing – review and editing. X-YL: Data curation, Formal Analysis, Methodology, Project administration, Software, Writing – review and editing. ZX-Z: Data curation, Formal Analysis, Investigation, Methodology, Project administration, Software, Writing – original draft. C-YX-Y: Data curation, Formal Analysis, Investigation, Methodology, Writing – original draft. Y-TT: Data curation, Investigation, Methodology, Resources, Software, Writing – original draft. Y-TM: Data curation, Formal Analysis, Investigation, Methodology, Software, Writing – original draft. H-JL: Data curation, Formal Analysis, Investigation, Project administration, Software, Writing – original draft. T-YG: Data curation, Formal Analysis, Investigation, Methodology, Project administration, Software, Writing – original draft. XL: Data curation, Formal Analysis, Investigation, Software, Validation, Writing – original draft. JL: Conceptualization, Investigation, Methodology, Project administration, Resources, Visualization, Writing – review and editing. CZ: Conceptualization, Data curation, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Writing – original draft, Writing – review and editing. S-LH: Conceptualization, Data curation, Methodology, Project administration, Resources, Software, Writing – review and editing.

 Funding

The author(s) declare that financial support was received for the research and/or publication of this article. This study was supported by the Leading scientific research projects of Shiyan City in 2021 (No. 21Y16) and the College students Innovation and entrepreneurship training program project from Hubei University of Medicine in 2022 (No. X202213249005).

 Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

 Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

 Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2025.1500475/full#supplementary-material

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