Third-Generation Antiseizure Medications for Adjunctive Treatment of Focal-Onset Seizures in Adults: A Systematic Review and Network Meta-analysis.

BACKGROUND: Brivaracetam (BRV), cenobamate (CNB), eslicarbazepine acetate (ESL), lacosamide (LCM) and perampanel (PER) are antiseizure medications (ASMs) approved for adjunctive treatment of focal-onset seizures. So far, no randomised controlled trial directly compared the efficacy and safety of these drugs.
OBJECTIVE: We estimated the comparative efficacy and safety of these ASMs for the treatment of focal-onset seizures in adults with epilepsy using a network meta-analysis (NMA).
METHODS: We systematically searched (June week 4, 2021) MEDLINE (accessed by PubMed), the Cochrane Central Register of Controlled Trials (CENTRAL), and the US National Institutes of Health Clinical Trials Registry ( http://www.clinicaltrials.gov ). There were no date limitations or language restrictions. Randomised, double-blinded, controlled, parallel-group, add-on studies that compared oral BRV, CNB, ESL, LCM, and PER versus any comparator over maintenance periods of at least 12 weeks and included adult patients with focal seizures uncontrolled by concomitant ASMs were identified. The efficacy outcomes were the proportions of patients with ≥ 50% and 100% reduction in baseline seizure frequency during the maintenance period. The tolerability outcomes were the proportions of participants who experienced at least one treatment-emergent adverse event (TEAE) and experienced at least one TEAE leading to discontinuation. Effect sizes were estimated by network meta-analyses within a frequentist framework. The hierarchy of competing interventions was established using the surface under the cumulative ranking curve (SUCRA).
RESULTS: Sixteen trials (BRV: n = 3, CNB: n = 1, ESL: n = 4, LCM: n = 4, PER: n = 4) were included, overall enrolling 4507 patients randomised to add-on active treatments (BRV = 803, CNB = 221, ESL =9 90, LCM = 1104, and PER = 1389) and 2246 to add-on placebo. Cenobamate was associated with a higher rate of ≥ 50% seizure frequency reduction than BRV [odds ratio (OR) 2.02, 95% confidence interval (CI) 1.11-3.66], ESL (OR 1.93, 95% CI 1.07-3.48), LCM (OR 1.86, 95% CI 1.04-3.32), and PER (OR 2.07, 95% CI 1.16-3.70). There was a not statistically significant trend favouring CNB over ESL, LCM and PER for the seizure freedom outcome. Brivaracetam (OR 0.61, 95% CI 0.44-0.86) and LCM (OR 0.60, 95% CI 0.40-0.88) were associated with a lower proportion of participants experiencing TEAEs compared to ESL, and patients treated with PER were associated with a higher risk to experience at least one TEAE (OR 1.42, 95% CI 1.02-1.96) than BRV. According to SUCRA, CNB had the greatest likelihood of being the best option for the ≥ 50% and 100% seizure frequency reduction, and BRV and LCM had the highest probabilities of being the best-tolerated treatments.
CONCLUSIONS: Cenobamate ranked best for efficacy, and BRV and LCM were best tolerated over the other comparators. Although NMAs cannot replace direct comparisons, they may support physicians in clinical decision making.

Key Points

Introduction

Epilepsies are among the most common chronic disorders of the brain and affect approximately 70 million people worldwide [1-3]. The management of epilepsy is mainly symptomatic, aimed at reducing the risk of seizure recurrence, and antiseizure medications (ASMs) are the mainstay of treatment. However, more than 50% of patients do not achieve seizure freedom with initial monotherapy [4-7], and treatment options for these patients include other ASM monotherapies or combination therapy using additional ASMs as adjunctive therapy. Focal onset seizures are the most prevalent type of seizures and can pose a significant risk to individual health and impair quality of life, particularly when they are associated with impairment of awareness.

Five ‘‘third-generation’’ ASMs were approved for adjunctive treatment of focal onset seizures in adult patients during the past 10 years: lacosamide (LCM), eslicarbazepine acetate (ESL), perampanel (PER), brivaracetam (BRV), and cenobamate (CNB) [8]. So far, however, there has not been a single randomised controlled trial (RCT) performed to directly compare the efficacy and safety of these drugs. Here, we assessed the comparative efficacy and safety of these ASMs using a network meta-analysis (NMA).

Methods

Search Strategy

The results were reported according to the recommendations of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) extension statement for network meta-analyses [9]. We systematically searched (June, Week 4, 2021) MEDLINE (accessed by PubMed), the Cochrane Central Register of Controlled Trials (CENTRAL), and the US National Institutes of Health Clinical Trials Registry (http://www.clinicaltrials.gov). The search terms were (lacosamide OR perampanel OR brivaracetam OR eslicarbazepine OR cenobamate) AND (epilepsy OR seizure); further details of search strategies are outlined in the Appendix I of the electronic supplementary material (SI). There were no date limitations or language restrictions. The reference lists of retrieved studies were reviewed to identify additional reports of relevant trials. The protocol was not registered previously.

Eligibility Criteria

Randomised, double-blinded, controlled, parallel-group, add-on studies that compared oral BRV, CNB, ESL, LCM, and PER versus any comparator over maintenance periods (or periods of stable dosing for dose-escalation trials) of at least 12 weeks and included adult patients with focal epilepsy and seizures uncontrolled by one or more concomitant ASMs.

Outcome Measures

The efficacy outcomes were the proportion of patients with ≥ 50% (seizure response) and 100% (seizure freedom) reduction in monthly seizure frequency during the maintenance treatment period compared with the pre-randomisation baseline; if data over the maintenance period were not reported, the treatment period was used. The modified intent-to-treat (mITT) population data were used for the efficacy analyses. The mITT analysis set consisted of all randomised patients who received at least one dose of the study drug and had any seizure frequency data collected during the double-blind phase. For the seizure freedom outcome, when data were available, we adopted the “pragmatic ITT” approach, whereby only patients who complete the study and are seizure-free can be classed as seizure-free in the numerator and the mITT is used as denominator [10].

The tolerability outcomes included the proportions of participants who experienced at least one treatment-emergent adverse event (TEAE) and experienced at least one TEAE leading to discontinuation. The safety population, which included all randomly assigned patients, was considered for the tolerability analyses. For each ASM, only licensed, maintenance daily doses for adjunctive therapy of focal onset seizures in adults according to individual summaries of product characteristics (i.e., BRV 50–200 mg, CNB 200–400 mg, ESL 800–1200 mg, LCM 200–400 mg, and PER 4-12 mg) were considered [11-15].

Study Selection, Data Extraction, Assessment of the Risk of Bias and Confidence in the Evidence

Two review authors independently assessed trials for inclusion and extracted the following information from included studies: main study author and date of publication, methodology and trial design (methods of randomisation, allocation concealment and blinding, duration of baseline and treatment periods, dose/s of ASMs tested), number and demographics of participants (age, sex, ethnicity, concomitant ASMs, seizure frequency during the baseline period), and the number of patients experiencing any outcome per randomised group. Any disagreement was resolved by discussion with a third review author. The risk of bias of the identified studies was assessed following the recommendations of the Cochrane Collaboration [16]. We judged the confidence in the evidence derived from NMA using the web application CINeMA (http://cinema.ispm.ch/) [17].

Statistical Analysis

First, pairwise meta-analyses were performed for all outcomes, using a fixed-effects model. Second, network meta-analyses within a frequentist framework were done assuming equal heterogeneity parameter τ across all comparisons [18]. For studies with more than one randomised treatment arm within the licensed maintenance daily doses, the arms were pooled to form a single node for the corresponding ASM. Where sufficient data were available, secondary analyses were performed according to daily dosages with each dose within the licensed maintenance daily doses of any ASM representing a separate node in the network. It is appropriate to use NMA if the assumption of transitivity (distributions of the potential effect modifiers, like study and patient-level covariates, are balanced across all pairwise comparisons) can be defended [19]. We assessed the transitivity assumption by looking at the similarities of studies in each comparison. We used the loop-specific approach to evaluate coherence locally, defined as the statistical agreement between direct and indirect evidence for a specific comparison (consistency assumption) [20]. Coherence could only be assessed for the secondary analyses by doses and not for the primary analyses as there were no closed loops in the 'primary' networks. Effect sizes were estimated as odds ratios (ORs) with their 95% confidence intervals (CIs). The hierarchy of competing interventions was established using the surface under the cumulative ranking curve (SUCRA) and mean ranks. Data analysis was performed using STATA/IC 13.1 statistical package (StataCorp LP, College Station, TX, USA).

Results

Results of the Search and Characteristics of Included Studies

Database and trial register searching identified a total of 1100 records; 16 RCTs trials were included in the qualitative and quantitative synthesis [21-36] (Fig. 1).

Fig. 1

Study flow diagram. CENTRAL Cochrane Central Register of Controlled Trials

All 16 RCTs were placebo-controlled studies and assessed both the efficacy and safety of the investigational drug (BRV: n = 3, CNB: n = 1, ESL: n = 4, LCM: n = 4, PER: n = 4). All studies had a titration phase, apart from three BRV trials; the maintenance period was 12 weeks in eleven studies, 13 weeks in four studies and 14 weeks in one study. Details of the studies are provided in Table 1. The studies recruited 6753 patients, of which 4507 were randomised to active treatments (BRV = 803, CNB = 221, ESL = 990, LCM = 1104, and PER = 1389) and 2246 to placebo. Participants enrolled across the studies were similar in terms of average age, sex distribution, epilepsy duration, concomitant ASMs with most patients treated with two or more ASMs, and baseline seizure frequency. Characteristics of the participants are summarised in Table 2; details of the type of concomitant ASMs are provided in Table e-1 in the SI.

Table 1

Characteristics of the included studies

Study [Reference]	Study design	Main inclusion criteria	Treatment arms
Biton et al. (2014) [21]	Multicentre, multinational (Australia, Brazil, Canada, Mexico, USA)	Aged 16–70 years Focal epilepsy uncontrolled despite treatment with one or two ASMs At least 2 focal seizures/month during the 3 months before screening and at least 8 focal seizures during the 8-week baseline period Current treatment on a stable dose of 1–2 ASMs for at least 4 weeks before screening	Placebo, BRV: 5, 20, 50 mg daily
	Parallel-group, randomised, placebo-controlled trial:  8-week observational baseline period  12-week maintenance phase
Ryvlin et al. (2014) [22]	Multicentre, multinational (Belgium, Finland, France, Germany, Hungary, India, Italy, Poland, Spain, Switzerland, The Netherlands, UK)	Aged 16–70 years Focal epilepsy uncontrolled despite treatment with one or two ASMs At least 2 focal seizures/month during the 3 months before screening and at least 8 focal seizures during the 8-week baseline period Current treatment on a stable dose of 1–2 ASMs for at least 4 weeks before screening	Placebo, BRV: 20, 50, 100 mg daily
	Parallel-group, randomised, placebo-controlled trial:  8-week observational baseline period  12-week maintenance phase
Klein et al. (2015) [23]	Multicentre, multinational (Austria, Belgium, Brazil, Bulgaria, Canada, Czech Republic, Estonia, Finland, France, Germany, Hong Kong, Hungary, India, Italy, Japan, Latvia, Lithuania, Mexico, Poland, Puerto Rico, Republic of Korea, Russia, The Netherlands, Spain, Sweden, Taiwan, UK, USA)	Aged 16–80 years Focal epilepsy uncontrolled despite treatment with one or two ASMs At least 2 focal seizures/month during the 3 months before screening and at least 8 focal seizures during the 8-week baseline period Current treatment on a stable dose of 1–2 ASMs for at least 4 weeks before screening	Placebo, BRV: 100, 200 mg daily
	Parallel-group, randomised, placebo-controlled trial:  8-week observational baseline period  12-week maintenance phase
Krauss et al. (2019) [24]	Multicentre, multinational (Australia, Bulgaria, Czech Republic, France, Germany, Hungary, Israel, Poland, Romania, Serbia, South Korea, Spain, Thailand, Ukraine, UK, USA)	Aged 18–70 years Focal epilepsy uncontrolled despite treatment with at least one ASM within the past 2 years At least 8 focal seizures with a seizure-free interval fewer than 25 days during the 8-week baseline assessment with at least 3 of these seizures occurring during each of the two consecutive 4-week segments of the baseline period Current treatment on a stable dose of 1–3 ASMs for at least 4 weeks before screening	Placebo, CNB: 100, 200, 400 mg daily
	Parallel-group, randomised, placebo-controlled trial:  8-week observational baseline period  6-week titration phase  12-week maintenance phase
Elger et al. (2009) [25]	Multicentre, multinational (Austria, Croatia, Czech Republic, Germany, Hungary, Lithuania, Poland, Romania, Russia, Switzerland)	Aged 18 years or older Focal onset seizures for a minimum of 12 months before screening At least 4 focal seizures in the two 4-week periods of the 8-week baseline period with no seizure-free interval >21 consecutive days Current treatment on a stable dose of 1–2 ASMs for at least 2 months before screening	Placebo, ESL: 400, 800, 1200 mg daily
	Parallel-group, randomised, placebo-controlled trial:  8-week observational baseline period  2-week titration phase 12-week maintenance phase
Gil-Nagel et al. (2009) [26]	Multicentre, multinational (Mexico, Portugal, Spain)	Aged 18 years or older Focal onset seizures for a minimum of 12 months before screening At least 4 focal seizures in the two 4-week periods before screening as well as during each of the 4-weeks periods of the 8-week baseline period Current treatment on a stable dose of 1–2 ASMs for at least 2 months before screening	Placebo, ESL: 800, 1200 mg daily
	Parallel-group, randomised, placebo-controlled trial:  8-week observational baseline period  2-week titration phase  12-week maintenance phase
Ben-Menachem et al. (2010) [27]	Multicentre, multinational (Argentina, Australia, Belgium, Brazil, Denmark, Germany, The Netherlands, Portugal, Romania, South Africa, Spain, Sweden, UK)	Aged 18 years or older Focal onset seizures for a minimum of 12 months before screening At least 4 focal seizures in the two 4-week periods before screening as well as during each of the two 4-week periods of the 8-week baseline period Current treatment on a stable dose of 1–3 ASMs for at least 2 months before screening	Placebo, ESL: 400, 800, 1200 mg daily
	Parallel-group, randomised, placebo-controlled trial:  8-week observational baseline period  14-week maintenance phase
Sperling et al. (2015) [28]	Multicentre, multinational (Argentina, Australia, Belgium, Brazil, Canada, Cyprus, France, Germany, Greece, Hungary, India, Italy, Poland, Turkey, South Korea, Romania, South Africa, Ukraine, US)	Aged 16 years or older Focal onset seizures for a minimum of 12 months before screening At least 4 focal seizures within the 4-week period before screening and at least 8 focal seizures during the baseline period (with ≥ 3 seizures during each 4-week period and no seizure-free interval exceeding 28 consecutive days) Current treatment on a stable dose of 1–2 ASMs for at least 1 month before screening	Placebo, ESL: 800, 1200 mg daily
	Parallel-group, randomised, placebo-controlled trial:  8-week observational baseline period  2-week titration phase  12-week maintenance phase
Ben-Menachem et al. (2007) [29]	Multicentre, multinational (Germany, Hungary, Lithuania, Poland, Switzerland, UK, USA)	Aged 18–65 years Focal onset seizures for at least the preceding 2 years despite treatment with at least two ASMs At least 4 focal seizures per 28 days on average, with no seizure-free period longer than 21 days during the 8-week baseline period Current treatment on a stable dose of 1–2 ASMs in the 4 weeks before enrolment and during the baseline period	Placebo, LCM: 200, 400, 600 mg daily
	Parallel-group, randomised, placebo-controlled trial:  8-week observational baseline period  6-week titration phase  12-week maintenance phase
Halász et al. (2009) [30]	Multicentre, multinational (Australia, Croatia, Czech Republic, Finland, France, Germany, Hungary, Lithuania, Poland, Russia, Spain, Sweden, UK)	Aged 16–70 years Focal onset seizures for at least the preceding 2 years despite treatment with at least two ASMs At least 4 focal seizures per 28 days on average, with no seizure-free period longer than 21 days during the 8-week period before enrolment as well as during the 8-week baseline period Current treatment on a stable dose of 1–3 ASMs in the 4 weeks before enrolment and during the baseline period	Placebo, LCM: 200, 400 mg daily
	Parallel-group, randomised, placebo-controlled trial:  8-week observational baseline period  4-week titration phase  12-week maintenance phase
Chung et al. (2010) [31]	Multicentre, national (USA)	Aged 16–70 years Focal onset seizures for at least the preceding 2 years despite treatment with at least two ASMs At least 4 focal seizures per 28 days, with no seizure-free period longer than 21 days during the 8-week baseline period Current treatment on a stable dose of 1–3 ASMs in the 4 weeks before enrolment and during the baseline period	Placebo, LCM: 400, 600 mg daily
	Parallel-group, randomised, placebo-controlled trial:  8-week observational baseline period  6-week titration phase  12-week maintenance phase
Hong et al. (2016) [32]	Multicentre, multinational (China, Japan)	Aged 16–70 years Focal onset seizures for at least the preceding 2 years despite treatment with at least two ASMs At least 4 focal seizures with motor sign per 28 days and no seizure-free period or longer than 21 days during the 8 weeks before baseline Current treatment on a stable dose of 1–3 ASMs in the 4 weeks before entry into the baseline period	Placebo, LCM: 200, 400 mg daily
	Parallel-group, randomised, placebo-controlled trial:  8-week observational baseline period  4-week titration phase  12-week maintenance phase
French et al. (2012) [33]	Multicentre, multinational (Argentina, Canada, Chile, Mexico, USA)	Aged 12 years or older Focal onset seizures despite treatment with at least two ASMs within the past 2 years At least 5 focal seizures in the 6-week baseline period, with ≥ 2 focal seizures per each of 3-week period and no seizure-free interval exceeding 25 days Current treatment on a stable dose of 1–3 ASMs for at least 3 weeks before randomisation	Placebo, PER: 8, 12 mg daily
	Parallel-group, randomised, placebo-controlled trial:  6-week observational baseline period  6-week titration phase  13-week maintenance phase
Krauss et al. (2012) [35]	Multicentre, multinational (Australia, Bulgaria, Czech Republic, Estonia, Germany, Hong Kong, Hungary, India, Italy, Latvia, Lithuania, Malaysia, Philippines, Poland, Portugal, Republic of Korea, Romania, Russia, Serbia, Spain, Taiwan, Thailand, Ukraine)	Aged 12 years or older Focal onset seizures despite treatment with at least two ASMs within the past 2 years At least 5 focal seizures in the 6-week baseline period, with ≥ 2 focal seizures per each of 3-week period and no seizure-free interval exceeding 25 days Current treatment on a stable dose of 1–3 ASMs for at least 3 weeks before randomisation	Placebo, PER: 2, 4, 8 mg daily
	Parallel-group, randomised, placebo-controlled trial:  6-week observational baseline period  6-week titration phase  13-week maintenance phase
French et al. (2013) [34]	Multicentre, multinational (Australia, Austria, Belgium, Germany, Finland, France, UK, Greece, India, Israel, Italy, The Netherlands, Russia, South Africa, Sweden, USA)	Aged 12 years or older Focal onset seizures despite treatment with at least two ASMs within the past 2 years At least 5 focal seizures in the 6-week baseline period, with ≥ 2 focal seizures per each of 3-week period and no seizure-free interval exceeding 25 days Current treatment on a stable dose of 1–3 ASMs for at least 3 weeks before randomisation	Placebo, PER: 8, 12 mg daily
	Parallel-group, randomised, placebo-controlled trial:  6-week observational baseline period  6-week titration phase  13-week maintenance phase
Nishida et al. (2017) [36]	Multicentre, multinational (Australia, China, Japan, Malaysia, Republic of Korea, Taiwan, Thailand)	Aged 12 years or older Focal onset seizures despite treatment with at least two ASMs within the past 2 years At least 5 focal seizures in the 6-week baseline period, with ≥ 2 focal seizures per each of 3-week period and no seizure-free interval exceeding 25 days Current treatment on a stable dose of 1–3 ASMs	Placebo, PER: 4, 8, 12 mg daily
	Parallel-group, randomised, placebo-controlled trial:  6-week observational baseline period  6-week titration phase  13-week maintenance phase

ASM antiseizure medication, BRV brivaracetam, CNB cenobamate, ESL eslicarbazepine acetate, LCM lacosamide, PER perampanel.

Table 2

Characteristics of the study participants

Study	Treatment Arm	Number of participants	Age, years	Male sex, n (%)	Epilepsy duration,years	Number of concomitant ASMs, n (%)			Baseline seizure frequency per 28 days
						One	Two	Three or more
Biton et al. (2014) [21]	PBO	98	37.5 (12.6)	43 (43.9)	24.3 (12.2)	13 (13.3)	80 (81.6)	4 (4.1)	2.6 [1.6–4.5]**
	BRV50	101	38.9 (12.3)	51 (50.5)	26.2 (12.0)	13 (12.9)	82 (81.2)	6 (5.9)	2.9 [1.5–7.2]**
Ryvlin et al. (2014) [22]	PBO	100	36.4 (13.0)	54 (54.0)	20.4 (12.3)	14 (14.0)	83 (83.0)	3 (3.0)	2.07 [1.35–6.04]**
	BRV50	99	38.9 (13.6)	54 (54.5)	22.3 (13.0)	20 (20.2)	77 (77.8)	2 (2.0)	1.80 [1.25–3.47]**
	BRV100	100	38.0 (13.1)	58 (58.0)	22.1 (12.8)	16 (16.0)	77 (77.0)	7 (7.0)	2.02 [1.26–3.25]**
Klein et al. (2015) [23]	PBO	261	39.8 (12.5)	133 (50.1)	22.7 (13.3)	14 (14.0)	83 (83.0)	3 (3.0)	10.0 (3, 560)
	BRV100	253	39.1 (13.4)	102 (40.3)	22.2 (13.3)	20 (20.2)	77 (77.8)	2 (2.0)	9.5 (2, 354)
	BRV200	250	39.8 (12.8)	133 (53.2)	23.4 (14.6)	16 (16.0)	77 (77.0)	7 (7.0)	9.3 (3, 710)
Krauss et al. (2019) [24]	PBO	108	39.6 (12.4)	58 (53.7)	23.0 (14.2)	27 (25.0)	54 (50.0)	27 (25.0)	8.4 [6.0–19.0
	CNB200	110	40.9 (12.4)	54 (49.1)	22.8 (13.2)	39 (35.5)	47 (42.7)	24 (21.8)	11.0 [6.0–26.0]
	CNB400	111	39.6 (10.3)	52 (46.8)	24.4 (14.2)	24 (21.6)	62 (55.9)	25 (22.5)	9.0 [6.0–21.5]
Elger et al. (2009) [25]	PBO	102	37.0 (11.9)	48 (47.1)	19.4 (12.6)	34 (33.3)	67 (65.7)	1 (1.0)	12.4 (17.9)
	ESL800	98	41.3 (12.0)	54 (55.1)	23.1 (13.5)	31 (31.6)	67 (68.4)	0	11.2 (11.2)
	ESL1200	102	38.4 (11.7)	44 (43.1)	20.4 (11.9)	39 (38.2)	63 (61.8)	0	11.6 (15.9)
Gil-Nagel et al. (2009) [26]	PBO	87	37.7 (12.1)	43 (49.4)	23.8 (13.0)	16 (18.4)	66 (75.9)	5 (5.7)	11.3 (18.5)
	ESL800	85	36.8 (10.7)	35 (41.2)	22.5 (11.8)	22 (25.9)	58 (68.2)	5 (5.9)	11.6 (22.1)
	ESL1200	80	36.0 (11.4)	35 (43.8)	23.0 (13.0)	12 (15.0)	63 (78.8)	5 (6.3)	11.3 (10.3)
Ben-Menachem et al. (2010) [27]	PBO	100	36.7 (12.2)	52 (52.0)	25.4 (13.1)	15 (15.0)	76 (76.0)	9 (9.0)	14.3 (16.6)
	ESL800	101	36.4 (12.6)	51 (50.5)	22.4 (11.6)	17 (16.8)	73 (72.3)	11 (10.9)	16.5 (19.6)
	ESL1200	98	36.9 (11.6)	52 (53.1)	23.0 (12.9)	20 (20.4)	68 (69.4)	10 (10.2)	14.8 (16.0)
Sperling et al. (2015) [28]	PBO	224	39.0 (16, 67)	112 (50.0)	21.3 (14.6)	64 (28.6)	158 (70.5)	1 (0.4)	8 (4, 282)
	ESL800	216	38.5 (16, 71)	109 (50.5)	21.6 (13.0)	60 (27.8)	153 (70.8)	0	8 (1, 420)
	ESL1200	210	38.0 (16, 69)	105 (50.0)	21.2 (13.0)	59 (28.1)	151 (71.9)	0	9 (4, 351)
Ben-Menachem et al. (2007) [29]	PBO LCM200 LCM400	97 107 108	38.9 (11.1) 39.9 (11.7) 41.2 (11.6)	47 (48.5) 46 (43.0) 53 (49.1)	24.6 (11.8) 25.1 (12.9) 24.7 (13.1)	16% and 84% of the patients were taking 1 and 2 ASMs			Median seizure frequency ranged from 11 to 13 across all arms
Halász et al. (2009) [30]	PBO	163	38.5 (10.9)	91 (55.8)	21.1 (12.2)	21 (13.2)	82 (51.6)	56 (35.2)	9.9*
	LCM200	163	36.9 (11.7)	90 (55.2)	22.9 (12.3)	17 (10.6)	77 (48.1)	66 (41.3)	11.5*
	LCM400	159	37.9 (13.0)	69 (43.4)	22.8 (13.2)	25 (15.8)	79 (50.0)	54 (34.2)	10.3*
Chung et al. (2010) [31]	PBO	104	38.1 (12.0)	49 (47.1)	25.4 (13.3)	18 (17.3)	54 (51.9)	32 (30.8)	15.0*
	LCM400	204	39.1 (12.4)	104 (51.0)	24.5 (13.2)	36 (17.9)	110 (54.7)	55 (27.4)	11.5*
Hong et al. (2016) [32]	PBO	184	31.8 (12.0)	102 (55.4)	16.8 (11.5)	41 (22.4)	71 (38.8)	71 (38.8)	10.5 (3.6, 707.6)
	LCM200	183	33.2 (12.2)	94 (51.4)	18.3 (10.9)	45 (24.7)	79 (43.4)	58 (31.9)	11.0 (3.7, 1118.0)
	LCM400	180	32.3 (11.9)	104 (57.8)	17.9 (11.7)	35 (19.6)	81 (45.3)	63 (35.2)	10.0 (2.6, 221.0)
French et al. (2012) [33]	PBO	121	35.6 (14.7)	54 (44.6)	24.1 (12.9)§	15 (12.4)	64 (52.9)	42 (34.7)	13.7 (3.3, 227.4)
	PER8	133	35.8 (14.2)	65 (48.9)	23.6 (13.5)§	26 (19.5)	70 (52.9)	37 (27.8)	14.3 (2.4, 1030.8)
	PER12	134	36.7 (14.6)	69 (51.5)	23.3 (14.4)§	19 (14.2)	82 (61.2)	33 (24.6)	12.0 (2.9, 1083.1)
Krauss et al. (2012) [35]	PBO	185	33.4 (12.6)	95 (51.4)	17.5 (10.7)§	28 (15.1)	90 (48.6)	67 (36.2)	9.3 (3.3, 569.1)
	PER4	172	33.6 (12.2)	88 (51.2)	19.7 (12.1)§	19 (11.0)	88 (51.2)	65 (37.8)	10.0 (2.9, 4503.9)
	PER8	169	34.6 (12.8)	77 (45.6)	20.0 (11.9)§	27 (16.0)	82 (48.5)	60 (35.5)	10.9 (3.4, 723.2)
French et al. (2013) [34]	PBO PER8	136 129	34.4 (13.6) 36.7 (14.4)	71 (52.2) 65 (50.4)	22.0 (12.9)§ 22.5 (13.6)§	17 (12.5) 16 (12.4)	64 (47.1) 68 (52.7)	71 (52.2) 83 (64.3)	11.8 (3.4, 358.4) 13.0 (3.3, 652.2)
	PER12	121	35.5 (14.1)	50 (41.3)	21.3 (13.2)§	9 (7.4)	63 (52.1)	80 (66.1)	13.7 (1.4, 598.4)
Nishida et al. (2017) [36]	PBO	175	34.5 (13.2)	86 (49.1)	17.5 (10.9)	11 (6.3)	67 (38.3)	97 (55.4)	Median seizure frequency ranged from 9.1 to 10.0 across all arms
	PER8	175	33.6 (14.1)	91 (52.0)	16.9 (11.5)	15 (8.6)	60 (34.3)	100 (57.1)
	PER12	180	32.3 (12.3)	87 (48.3)	17.4 (11.2)	13 (7.2)	75 (41.7)	92 (51.1)

Data are mean (SD), median [IQR] or median (min, max) unless otherwise specified. *Median. **Baseline seizure frequency per week. §Converted to years by dividing the number of months by 12

ASM antiseizure medication, BRV brivaracetam, CNB cenobamate, ESL eslicarbazepine acetate, IQR interquartile range, LCM lacosamide, PER perampanel, SD standard deviation

Fifteen trials were considered to have used adequate methods of random sequence generation and allocation concealment; conversely, we judged one study to have an unclear risk of selection bias as study authors failed to provide details regarding methods used for allocation concealment [29]. We judged all included trials at low risk of performance and detection bias since blinding was ensured by matching placebo, and patients, investigators, and study personnel were all masked to the treatment assignment. Regarding the risk of attrition bias, patients lost to follow-up and withdrawals with corresponding reasons were documented in all trials. Studies presenting differences between intervention groups in the proportions of imputed outcome data for the responder rate outcome were judged to have an unclear risk of bias [21, 23, 25, 28–36]. There was no suspicion of selective outcome reporting across the trials. A summary of bias assessment risk is reported in Table e-2 in the SI.

Efficacy Outcomes

All RCTs provided data on the proportion of patients with ≥ 50% and 100% reduction in monthly seizure frequency from baseline. Most studies reported efficacy outcomes over the maintenance period, apart from one ESL study [27], for which treatment period was considered. In the CNB study [24], the mITT population for the responder rate outcome included patients who completed the 6-week titration phase and took at least one dose of study drug in the maintenance phase and had maintenance phase seizure data (mITT maintenance phase population). In one BRV study [22], the ITT population, defined as all randomised subjects who received at least one dose of study medication, was available for the responder rate outcome. The “pragmatic ITT” data for the seizure freedom outcome were available in most trials; in three studies, outcome up to treatment discontinuation was used to impute the seizure-freedom status for the remainder of the trial [25, 28, 36]. The network plots of treatment comparisons for the efficacy outcomes are shown in Figs. e-1 and e-2 in the SI.

At the pairwise meta-analyses, all ASMs were associated with a higher responder rate than placebo, and BRV, CNB, ESL, and PER were associated with a higher rate of seizure freedom than placebo (Table e-3 in the SI). In the analysis by dosages, ESL at 1200 mg/day was associated with a higher responder rate than ESL at 800 mg/day; LCM at 400 mg/day was associated with a higher responder rate than LCM at 200 mg/day, and PER at 8 and 12 mg/day was associated with a higher responder rate than PER at 4 mg/day (Table e-4 in the SI).

Results of the network meta-analyses of efficacy outcomes are shown in Figs. 2 and 3. Any ASM was more efficacious than placebo in the achievement of ≥50% reduction in baseline seizure frequency, and CNB was associated with a higher responder rate than BRV (OR 2.02, 95% CI 1.11–3.66), ESL (OR 1.93, 95% CI 1.07–3.48), LCM (OR 1.86, 95% CI 1.04–3.32), and PER (OR 2.07, 95% CI 1.16–3.70) (Fig. 2).

Fig. 2

Interval plot for the efficacy outcome: seizure response. BRV brivaracetam, CNB cenobamate, CI confidence interval, ESL eslicarbazepine acetate, LCM lacosamide, PBO placebo, PER perampanel

Fig. 3

Interval plot for the efficacy outcome: seizure freedom. BRV brivaracetam, CNB cenobamate, CI confidence interval, ESL eslicarbazepine acetate, LCM lacosamide, PBO placebo, PER perampanel

In the analysis by dosages (Table 3), CNB 400 mg/day was associated with a higher responder rate than ESL 800 mg/day (OR 2.65, 95% CI 1.35–5.22), ESL 1200 mg/day (OR 1.99, 95% CI 1.03–3.90), BRV 50 mg/day (OR 2.84, 95% CI 1.34–6.03), BRV 100 mg/day (OR 2.20, 95% CI 1.10–4.40), BRV 200 mg/day (OR 2.34, 95% CI 1.15–4.79), LCM 200 mg/day (OR 2.72, 95% CI 1.38–5.34), PER 4 mg/day (OR 3.75, 95% CI 1.87–7.51), PER 8 mg/day (OR 2.31, 95% CI 1.19–4.48), and PER 12 mg/day (OR 2.01, 95% CI 1.02–3.96). Cenobamate 200 mg/day was associated with a higher responder rate than PER 4 mg/day (OR 2.67, 95% CI 1.35–5.29). Lacosamide 400 mg/day was associated with a higher seizure responder rate that LCM 200 mg/day (OR 1.42, 95% CI 1.09–1.85), ESL 1200 mg/day was associated with a higher seizure responder rate than ESL 800 mg/day (OR 1.34, 95% CI 1.03–1.74), and PER 8 mg/day (OR 1.63, 95% CI 1.19–2.22) and 12 mg/day (OR 1.86, 95% CI 1.32–2.63) was associated with a higher rate of ≥ 50% seizure frequency reduction than PER 4 mg/day. Perampanel at the daily dosage of 4 mg was associated with a lower rate of seizure responder than ESL 1200 mg/day (OR 0.53, 95% CI 0.34–0.82), BRV 100 mg/day (OR 0.59, 95% CI 0.37–0.93), and LCM 400 mg/day (OR 0.51, 95% CI 0.34–0.78).

Table 3

Network league table for the responder rate

In the lower triangle, the odds ratios have been estimated as treatment in higher order versus treatment in lower order from top to bottom, whereas in the upper triangle the direction of the effects is the opposite. Bold values indicate statistical differences

BRV50 brivaracetam 50 mg/day, BRV100 brivaracetam 100 mg/day, BRV200 brivaracetam 200 mg/day, CNB200 cenobamate 200 mg/day, CNB400 cenobamate 400 mg/day, ESL800 eslicarbazepine acetate 800 mg/day, ESL1200 eslicarbazepine acetate 1200 mg/day, LCM200 lacosamide 200 mg/day, LCM400 lacosamide 400 mg/day PBO placebo, PER4 perampanel 4 mg/day, PER8 perampanel 8 mg/day, PER12 perampanel 12 mg/day

With regard the seizure freedom outcome, the network meta-analyses showed BRV, CNB, ESL and PER as being more efficacious than placebo at a statistically significant level (Fig. 3). In the analysis by daily dosages (Table 4), there were no statistically significant differences between the ASMs.

Table 4

Network league table for the seizure freedom

In the lower triangle, the odds ratios have been estimated as treatment in higher order versus treatment in lower order from top to bottom, whereas in the upper triangle the direction of the effects is the opposite. Bold values indicate statistical differences.

BRV50 brivaracetam 50 mg/day, BRV100 brivaracetam 100 mg/day, BRV200 brivaracetam 200 mg/day, CNB200 cenobamate 200 mg/day, CNB400 cenobamate 400 mg/day, ESL800 eslicarbazepine acetate 800 mg/day, ESL1200 eslicarbazepine acetate 1200 mg/day, LCM200 lacosamide 200 mg/day, LCM400 lacosamide 400 mg/day PBO placebo, PER4 perampanel 4 mg/day, PER8 perampanel 8 mg/day, PER12 perampanel 12 mg/day

According to SUCRA, CNB had the greatest likelihood ranking best for both seizure response and seizure freedom (Table 5, Appendix II in the SI); in the analysis by drug dosages, CNB 400 mg/day was the option associated with the highest probability to be the most efficacious treatment (Table e-5 and Appendix III in the SI). Results from the loop-specific approach for efficacy outcomes are shown in Appendix IV, and there was no statistically significant incoherence in any loop. Confidence in the evidence for the efficacy outcomes is summarised in Appendix V in the SI.

Table 5

Ranking according to SUCRA and mean rank for the efficacy and tolerability outcomes

Treatment	SUCRA	Mean rank
Seizure response
Brivaracetam	46.2	3.7
Cenobamate	99.0	1.1
Eslicarbazepine acetate	53.4	3.3
Lacosamide	60.8	3.0
Perampanel	40.7	4.0
Placebo	0.0	6.0
Seizure freedom
Brivaracetam	72.4	2.4
Cenobamate	88.8	1.6
Eslicarbazepine acetate	47.2	3.6
Lacosamide	37.8	4.1
Perampanel	53.0	3.4
Placebo	0.8	6.0
At least one treatment-emergent adverse event
Brivaracetam	67.0	2.6
Cenobamate	21.5	4.9
Eslicarbazepine acetate	12.8	5.4
Lacosamide	70.2	2.5
Perampanel	29.6	4.5
Placebo	98.8	1.1
At least one treatment-emergent adverse event leading to discontinuation
Brivaracetam	62.3	2.9
Cenobamate	11.9	5.4
Eslicarbazepine acetate	24.8	4.8
Lacosamide	56.8	3.2
Perampanel	44.5	3.8
Placebo	99.7	1.0

SUCRA surface under the cumulative ranking curve

Higher SUCRA values correspond to higher probabilities of better efficacy/tolerability

Tolerability Outcomes

Fourteen RCTs provided data on the proportions of participants who experienced at least one TEAE, whereas RCTs two did not [30, 31]. All RCTs except one LCM study [31] provided data on the proportion of participants who experienced at least one TEAE leading to discontinuation. Figure e-1 in the SI shows the network plots of treatment comparisons for the tolerability and safety outcomes; the corresponding network plots according to treatment dosages are shown in Fig. e-2 in the SI.

At the pairwise meta-analyses, BRV, CNB, ESL, and PER were associated with a higher proportion of patients experiencing at least one TEAE compared to placebo, and the risk of TEAEs leading to treatment discontinuation was higher with any ASM in comparison to placebo (Table e-3 in the SI). In the analysis by dosages, the rate of patients experiencing TEAEs was higher with CNB 400 mg/day than with CNB 200 mg/day, ESL 1200 mg/day than with ESL 800, LCM 400 mg/day than with LCM 200 mg/day, PER 12 mg/day than with PER 4 mg/day, and PER 12 mg/day than with PER 8 mg/day, and the rate of patients experiencing at least one TEAE leading to discontinuation was higher with ESL 1200 mg/day than with ESL 800, LCM 400 mg/day than with LCM 200 mg/day, PER 8 mg/day than with PER 4 mg/day, PER 12 mg/day than with PER 4 mg/day, and PER 12 mg/day than with PER 8 mg/day (Table e-4 in the SI).

Results of the network meta-analyses of tolerability outcomes are shown in Figs. 4 and 5. Any ASM was associated with a higher rate of patients who experienced at least one TEAE in comparison to placebo; BRV (OR 0.61, 95% CI 0.44–0.86) and LCM (OR 0.60, 95% CI 0.40–0.88) were associated with a lower proportion of participants experiencing TEAEs in comparison to ESL, and PER was associated with a higher risk of experiencing at least one TEAE (OR 1.42, 95% CI 1.02–1.96) than BRV (Fig. 4). Any ASM was associated with a higher rate of patients who experienced at least one TEAE leading to discontinuation than placebo, whereas there were no statistically significant differences across the individual ASMs (Fig. 5).

Fig. 4

Interval plot for the tolerability outcome: at least one treatment-emergent adverse event. BRV brivaracetam, CNB cenobamate, CI confidence interval, ESL eslicarbazepine acetate, LCM lacosamide, PBO placebo, PER perampanel

Fig. 5

Interval plot for the tolerability outcome: at least one treatment-emergent adverse event leading to discontinuation. BRV brivaracetam, CNB cenobamate, CI confidence interval, ESL eslicarbazepine acetate, LCM lacosamide, PBO placebo, PER perampanel

In the analysis by dosages (Table 6), the rate of patients who experienced at least one TEAE was higher with ESL 1200 mg/day than with ESL 800 mg/day (OR 1.43, 95% CI 1.09–1.88) and PER 12 mg/day than with ESL 800 mg/day (OR 1.66, 95% CI 1.08–2.56), while it was lower with LCM 200 mg/day compared to ESL 800 mg/day (OR 0.55, 95% CI 0.35–0.86). In comparison to ESL 1200 mg/day, BRV 50 mg/day (OR 0.45, 95% CI 0.28–4.61), BRV 100 mg/day (OR 0.55, 95% CI 0.37–0.82), BRV 200 mg/day (OR 0.52, 95% CI 0.33–0.80), LCM 200 mg/day (OR 0.39, 95% CI 0.25–0.61), and PER 4 mg/day (OR 0.50, 95% CI 0.34–0.75) were associated with lower proportions of patients who experienced at least one TEAE. Compared to BRV 50 mg/day, PER 12 mg/day (OR 2.56, 95% CI 1.50–4.38) and CNB 400 mg/day (OR 3.23, 95% CI 1.38–7.56) showed a high risk of TEAE occurrence. Perampanel 12 mg/day and CNB 400 mg/day were associated with a higher rate of patients who experienced at least one TEAE compared to BRV 100 mg/day (PER 12 mg/day: OR 2.12, 95% CI 1.34–3.35; CNB 400 mg/day: OR 2.67, 95% CI 1.19–5.97) and BRV 200 mg/day (PER 12 mg/day: OR 2.24, 95% CI 1.37–3.66; CNB 400 mg/day: OR 2.82, 95% CI 1.24–6.44). The rates of patients experiencing TEAEs were higher with LCM 400 mg/day (OR 1.68, 95% CI 1.15–2.48), PER 8 mg/day (OR 1.85, 95% CI 1.18–2.89), PER 12 mg/day (OR 3.00, 95% CI 1.82–4.94), and CNB 400 mg/day (OR 3.77, 95% CI 1.65–8.65) in comparison to LCM 200 mg/day. The rate of patients with at least one TEAE was higher with PER 8 mg/day than PER 4 mg/day (OR 1.42, 95% CI 1.04–1.93), and with PER 12 mg/day than with PER 4 mg/day (OR 2.30, 95% CI 1.55–3.43), PER 8 mg/day (OR 1.62, 95% CI 1.13–2.33), and LCM 400 mg/day (OR 1.78, 95% CI 1.06–2.99). Cenobamate 400 mg/day was associated with a statistically significantly higher rate of patients with at least one TEAE than PER 4 mg/day (OR 2.90, 95% CI 1.30–6.48). Further, CNB 200 mg/day was associated with a lower rate of patients who experienced at least one TEAE compared to PER 12 (OR 0.45, 95% CI 0.22–0.90), and CNB 400 mg/day was associated with a higher rate of patients who experienced at least one TEAE compared to CNB 200 mg/day (OR 2.81, 95% CI 1.31–6.03).

Table 6

Network league table for the occurrence of at least one treatment-emergent adverse event

In the lower triangle, the odds ratios have been estimated as treatment in higher order versus treatment in lower order from top to bottom, whereas in the upper triangle the direction of the effects is the opposite. Bold values indicate statistical differences.

BRV50 brivaracetam 50 mg/day, BRV100 brivaracetam 100 mg/day, BRV200 brivaracetam 200 mg/day, CNB200 cenobamate 200 mg/day, CNB400 cenobamate 400 mg/day, ESL800 eslicarbazepine acetate 800 mg/day, ESL1200 eslicarbazepine acetate 1200 mg/day, LCM200 lacosamide 200 mg/day, LCM400 lacosamide 400 mg/day PBO placebo, PER4 perampanel 4 mg/day, PER8 perampanel 8 mg/day, PER12 perampanel 12 mg/day

Concerning the proportion of patients who experienced at least one TEAE leading to discontinuation according to daily dosages (Table 7), the rates were higher with ESL 1200 mg/day (OR 2.11, 95% CI 1.49–2.98) and PER 12 mg/day (OR 2.07, 95% CI 1.07–4.02). Compared with ESL 1200 mg/day, BRV 200 mg/day (OR 0.42, 95% CI 0.17–0.99), LCM 200 mg/day (OR 0.29, 95% CI 0.14–0.58), PER 4 mg/day (OR 0.23, 95% CI 0.10–0.52) and PER 8 mg/day (OR 0.51, 95% CI 0.27–0.97) were associated with a lower rate of patients experiencing at least one TEAE leading to discontinuation. The rates of participants experiencing TEAEs leading to discontinuation were higher with LCM 400 mg/day (OR 2.60, 95% CI 1.65–4.09), PER 12 mg/day (OR 3.44, 95% CI 1.66–7.16), and CNB 400 mg/day (OR 4.35, 95% CI 1.37–13.78) than with LCM 200 mg/day. Similarly, PER 8 mg/day (OR 2.25, 95% CI 1.19–4.26), PER 12 mg/day (OR 4.32, 95% CI 2.24–8.36), and CNB 400 mg/day (OR 5.46, 95% CI 1.60–18.67) were less tolerated than PER 4 mg/day. A higher rate of participants with TEAEs leading to discontinuation was associated with PER 12 mg/day than PER 8 mg/day (OR 1.92, 95% CI 1.29–2.86).

Table 7

Network league table for the occurrence of at least one treatment-emergent adverse event leading to discontinuation

In the lower triangle, the odds ratios have been estimated as treatment in higher order versus treatment in lower order from top to bottom, whereas in the upper triangle the direction of the effects is the opposite. Bold values indicate statistical differences.

BRV50 brivaracetam 50 mg/day, BRV100 brivaracetam 100 mg/day, BRV200 brivaracetam 200 mg/day, CNB200 cenobamate 200 mg/day, CNB400 cenobamate 400 mg/day, ESL800 eslicarbazepine acetate 800 mg/day, ESL1200 eslicarbazepine acetate 1200 mg/day, LCM200 lacosamide 200 mg/day, LCM400 lacosamide 400 mg/day PBO placebo, PER4 perampanel 4 mg/day, PER8 perampanel 8 mg/day, PER12 perampanel 12 mg/day

According to SUCRA, BRV and LCM had the highest probabilities of being the best-tolerated options among the individual ASMs for both the outcomes of the occurrence of any TEAE and TEAE leading to discontinuation (Table 5 and Appendix II in the SI); across the individual ASMs at the different dosages, LCM 200 mg/day was the option with the highest probability of being the most tolerated in terms of any TEAE occurrence, and PER 4 mg/day and LCM 200 mg/day were the options with the lowest likelihood of being associated with TEAEs leading to treatment discontinuation (Table e-5 and Appendix III in the SI). Results from the loop-specific approach for tolerability outcomes are shown in Appendix IV in the SI, and there was no statistically significant incoherence in any loop. Confidence in the evidence for the tolerability outcomes is shown in Appendix V in the SI.

Clustered ranking plots of the ASM network for the efficacy and tolerability outcomes for individual ASMs are shown in Figs. 6, 7, 8 and 9; the corresponding plots by daily dosages are shown in Fig. e-3 in the SI.

Fig. 6

Clustered ranking plot of the antiseizure medications network for the efficacy and tolerability outcomes: seizure response and occurrence of at least one treatment-emergent adverse event. Ranking plots are based on cluster analysis of SUCRA values for two different outcomes: efficacy and tolerability. Note: Y and X axes represent the cumulative ranking curve (SUCRA) to rank each intervention—i.e., probability between 0 to 1 of an intervention being superior in efficacy (X axis) or tolerability (Y axis). Higher SUCRA values correspond to higher probabilities of better efficacy/tolerability. Each colour represents a group of treatments that belong to the same cluster. BRV brivaracetam, CNB cenobamate, CI confidence interval, ESL eslicarbazepine acetate, LCM lacosamide, PBO placebo, PER perampanel, SUCRA surface under the cumulative ranking curve

Fig. 7

Clustered ranking plot of the antiseizure medications network for the efficacy and tolerability outcomes: seizure response and occurrence of at least one treatment-emergent adverse event leading to treatment discontinuation. Ranking plots are based on cluster analysis of SUCRA values for two different outcomes: efficacy and tolerability. Note: Y and X axes represent the cumulative ranking curve (SUCRA) to rank each intervention—i.e., probability between 0 to 1 of an intervention being superior in efficacy (X axis) or tolerability (Y axis). Higher SUCRA values correspond to higher probabilities of better efficacy/tolerability. Each colour represents a group of treatments that belong to the same cluster. BRV brivaracetam, CNB cenobamate, CI confidence interval, ESL eslicarbazepine acetate, LCM lacosamide, PBO placebo, PER perampanel, SUCRA surface under the cumulative ranking curve

Fig. 8

Clustered ranking plot of the antiseizure medications network for the efficacy and tolerability outcomes: seizure freedom and occurrence of at least one treatment-emergent adverse event. Ranking plots are based on cluster analysis of SUCRA values for two different outcomes: efficacy and tolerability. Note: Y and X axes represent the cumulative ranking curve (SUCRA) to rank each intervention—i.e., probability between 0 to 1 of an intervention being superior in efficacy (X axis) or tolerability (Y axis). Higher SUCRA values correspond to higher probabilities of better efficacy/tolerability. Each colour represents a group of treatments that belong to the same cluster. BRV brivaracetam, CNB cenobamate, CI confidence interval, ESL eslicarbazepine acetate, LCM lacosamide, PBO placebo, PER perampanel, SUCRA surface under the cumulative ranking curve

Fig. 9

Clustered ranking plot of the antiseizure medications network for the efficacy and tolerability outcomes: seizure freedom and occurrence of at least one treatment-emergent adverse event leading to treatment discontinuation. Ranking plots are based on cluster analysis of SUCRA values for two different outcomes: efficacy and tolerability. Note: Y and X axes represent the cumulative ranking curve (SUCRA) to rank each intervention—i.e., probability between 0 to 1 of an intervention being superior in efficacy (X axis) or tolerability (Y axis). Higher SUCRA values correspond to higher probabilities of better efficacy/tolerability. Each colour represents a group of treatments that belong to the same cluster. BRV brivaracetam, CNB cenobamate, CI confidence interval, ESL eslicarbazepine acetate, LCM lacosamide, PBO placebo, PER perampanel, SUCRA surface under the cumulative ranking curve

Discussion

Summary of Main Results

The analyses of efficacy outcomes considered in the current NMA indicated that adjunctive CNB was associated with a higher responder rate and the greatest likelihood ranking best for seizure freedom in comparison to add-on BRV, ESL, LCM, and PER.

So far, little has changed in the rate of patients who can achieve seizure control despite the development of many ASMs in the past few decades [37], and there is still the need for novel, more effective therapeutic options. Uncontrolled epilepsy is often disabling, with patients experiencing psychological and social dysfunction, reduced educational and employment prospects, impaired quality of life, and risk of premature death [38].

Cenobamate has recently been approved for the treatment of focal onset seizures in adults and is characterised by a so-far unique dual complementary mechanism of action. It decreases excitatory currents by inhibiting the persistent component of the sodium current and enhancing the inactivated state of voltage-gated sodium channels [39]. In addition, it enhances inhibitory currents through GABAA receptor allosteric modulation and experimental evidence suggests it may target both synaptic and extra-synaptic GABAA receptors [39-41]. The comparative analysis of preclinical antiseizure profiles of CNB and other ASMs targeting similar molecular targets suggests that CNB is a mechanistically novel drug [42]. The dual pharmacodynamic activities of CNB on targets regulating both excitatory and inhibitory neurotransmission may contribute to explain its broad preclinical activity and support its clinical efficacy in patients with focal epilepsy [42], although the drug may possess other yet unknown mechanisms of action. The rates of seizure response and seizure freedom observed with CNB compare very favourably with those of the other adjunctive ASMs and bring promise for patients who have difficult-to-control seizures, mainly if the higher dosage can be tolerated. Real-life data overcoming the constraints of the RCT design will complement and further clarify the true therapeutic potentialities and clinical relevance of this newest ASM.

The analyses of tolerability outcomes indicated the good profile of BRV and LCM over the other comparators. Brivaracetam and LCM were associated with a lower proportion of participants experiencing TEAEs in comparison to ESL, and patients treated with PER were associated with a higher risk of experiencing at least one TEAE than BRV. Overall, BRV and LCM had the highest probabilities of being the best-tolerated options for both the outcomes of the occurrence of any TEAE and TEAEs leading to discontinuation.

Brivaracetam is a rationally developed compound characterised by high-affinity binding to synaptic

vesicle protein 2A [43]. Lacosamide, the R-enantiomer of 2-acetamido-N-benzyl-3-methoxypropionamide, selectively enhances the slow inactivation of voltage-gated sodium channels [44]. Both BRV and LCM do not interact with most drug-metabolising enzymes and drug transporters and are associated with few clinically relevant drug-drug interactions [44, 45].

The good tolerability profile of BRV versus the other third-generation ASMs has been already demonstrated in prior indirect comparisons [46, 47]. In this regard, it is interesting that more than three-quarters of participants assigned to BRV treatment in the RCTs were taking sodium channel blockers (SCBs) as concomitant ASMs, and the risk of TEAEs in patients treated with BRV within the context of real-world clinical practice is significantly reduced by the concomitant use of an ASM acting as an SCB [48]. Although to date, there are no experimental data about any advantageous combinations of BRV with other ASMs, additive or synergic pharmacodynamic interactions between BRV and one or more compounds acting on voltage-gated sodium channels may exist and need to be specifically addressed. Further, the ranking of treatments according to tolerability outcomes suggested that the occurrence of any TEAE and the risk of TEAEs leading to discontinuation associated with BRV could not be dose dependent, while the incidence of TEAEs was higher with the increasing doses of CNB, ESL, LCM, and PER.

Both PER and BRV are among the ASMs traditionally associated with the strongest risk of behavioural adverse events. Although the incidence of these side effects is higher with PER than with BRV [49], the lack of analyses by individual TEAEs did not allow us to state whether the difference in the tolerability profile was driven by the risk of behavioural adverse events.

Also, LCM was associated with a lower proportion of patients experiencing at least one TEAE compared to ESL. Both LCM and ESL belong to the class of SCBs and reduce the voltage-gated sodium channels availability through enhancement of slow inactivation. However, it is worthy of note that distinctive characteristics exist between the two compounds, including the higher interaction of LCM with fast inactivation gating [50]. The possible contribution of such pharmacodynamic features to dictate differential tolerability in clinical practice has never been investigated and remains an attractive theme to explore.

Finally, CNB ranked as the treatment associated with the highest likelihood of TEAE occurrence, mainly at the highest daily dosage. In this regard, the rapid titration of 100 mg/week from 200 to 400 mg, and the impossibility as per study protocol to adjust the dose of concomitant ASMs, might have contributed to the higher rates of TEAEs in the 400 mg group. Interestingly, a slightly higher incidence of TEAEs has been observed among patients treated with CNB and concomitantly taking SCBs compared with those not taking them [51]. Further, as CNB inhibits cytochrome P450 (CYP), 2C19 and can inhibit or induce CYP2B6 and 3A4, pharmacokinetic drug-drug interactions occur; for example, CNB can increase plasma concentrations of desmethylclobazam, the active metabolite of clobazam, and a reduction in clobazam dose should be considered to avoid adverse events [39]. Considering the remarkable efficacy profile of CNB, it is important to be aware of the potential interactions with concomitant ASMs and ensure that patients are able to tolerate the introduction of the drug into the existing therapeutic regimen. Special caution and slow titration or stepwise tapering off should be considered in patients on other SCBs or GABA-ergic drugs to improve tolerability and minimise the risk of treatment failure due to TEAEs.

Strengths and Limitations

This NMA is the first to include CNB, the newest approved drug for treating focal-onset seizures, in comparative analyses of the efficacy and safety of ASMs and it updates the currently available systematic reviews of evidence [46, 47, 52]. Efficacy and safety analyses were performed according to actual licensed maintenance daily doses of ASMs and the estimates of seizure responder rates during the maintenance period can reflect steady-state drug levels at the target dose more accurately than data referring to the entire treatment phase, including the titration. The “pragmatic ITT” approach used for the seizure freedom outcome, which defines the percentage of seizure free completers, represents a more conservative method of measuring seizure freedom and provides more reliable and informative estimates of treatment efficacy as opposed to “last observation carried forward” methodology, whereby patients who were seizure-free up to dropping out of a study can be classed as being seizure-free [10]. Although the seizure-free numbers in add-on RCTs may not be predictive of seizure freedom in clinical practice, they do represent a reference point when assessing ASMs and an often-discussed marker of how potentially useful an ASM will be in refractory patients [10]. In this regard, the “pragmatic ITT” analysis more closely represents the information on seizure freedom that clinicians seek. Notably, only a few patients achieved seizure freedom in all included studies, and this may have led to a lack of sufficient statistical power to detect a significant difference between the comparators [53].

The validity of indirect comparisons relies upon the similarity and methodological quality of the individual RCTs being indirectly compared [54]. In the present NMA, we used strict inclusion criteria to minimize, as much as possible, any source of heterogeneity; all the included trials were overall clinically and methodologically homogeneous and comparable, and no trial showed a high risk of bias. Although there is no consensus about the optimal length of the treatment period, the inclusion of studies with a maintenance phase of 12 weeks or longer met the guideline on clinical investigation of medicinal products in the treatment of epileptic disorders, which recommends that the maintenance period should last at least 12 weeks to establish that efficacy is not short lasting [55]. However, despite the similarity of the included RCTs, some differences in characteristics of trials and populations such as treatment duration and concomitant medications need to be acknowledged. Studies with shorter double-blind treatment periods may have underestimated the occurrence of TEAEs compared to those with longer time frames available for tolerability assessment, and a higher burden of concomitant ASMs may have resulted in an increased frequency of TEAEs. Further, the lack of efficacy and tolerability data according to the mechanism of action of concomitant ASMs prevents to explore or confirm potential favourable or unfavourable drug interactions and combinations [48, 56].

The NMA also inherited the general limitations of the RCTs of adjunctive ASMs, including the short length of observation and the highly selected inclusion and exclusion criteria for enrolment, which do not account for the inherent variability of epilepsy and the need to tailor treatment according to individual characteristics, hence, limiting the external validity of the results. Although the ≥50% reduction in baseline seizure frequency represents one of the outcomes required for licensing studies, it lacks information on the actual effect of the treatment on the quality of life of patients. Further, the reliability of seizure count, as documented in clinical trials by self-reported calendar diaries, may be affected by issues like noncompliance with diary maintenance, poor accuracy in reporting, and limited awareness of seizures [57, 58]. Accordingly, studies considering patient-reported outcomes and new approaches for collecting reliable information about seizure control are warranted to fully assess the potential of treatments in the management of patients with epilepsy. In addition, all studies were funded by pharmaceutical companies. Importantly, data about efficacy and safety of CNB are obtained from one single trial and some of the results are associated with wide confidence intervals. In this regard, imprecision and uncertainty associated with low event rates can lead to extreme results and, in turn, influence the rankings of treatments. As ranks are sensitive to imprecision, dose-dependent relationships need to be interpreted with caution and no definitive conclusions can be drawn for trends that do not formally reach statistical significance. Finally, the protocol of this NMA was not registered previously, and the lack of information about economic issues does not allow to address cost-effectiveness analyses and provide further guidance for clinical decisions.

Conclusion

The comparative analyses of trials’ data have shown that CNB ranked best for efficacy outcomes standing out against the comparators, and BRV and LCM had the highest probabilities of being the best-tolerated options among the ASMs considered in this NMA. Ideally, head-to-head trials may allow definite conclusions on the comparative efficacy and tolerability of ASMs. It is unlikely that such RCTs will be performed. Although NMAs cannot replace studies directly comparing two or more drugs, they may offer reliable evidence of the relative efficacy and safety, provide useful information about the hierarchy of competing interventions, and may inform and guide physicians in clinical decision making [5, 59, 60].

Below is the link to the electronic supplementary material.

Supplementary file1 (PDF 2686 kb)

Brivaracetam, cenobamate, eslicarbazepine acetate, lacosamide, and perampanel are antiseizure medications approved for adjunctive treatment of focal-onset seizures.

Adjunctive cenobamate had the greatest likelihood of being the best option for the ≥ 50% and 100% seizure frequency reduction.

Adjunctive brivaracetam and lacosamide had the highest probabilities of being the best-tolerated treatments.