Optimal Dose of Erenumab for Preventive Treatment of Episodic Migraine: A Systematic Review and Meta-Analysis.

BACKGROUND: Erenumab is a novel monoclonal calcitonin gene-related peptide receptor antibody that is used for the preventive treatment of migraine.
OBJECTIVES: This study aimed to evaluate the overall safety, efficacy, and dose-response relationship of erenumab in patients with episodic migraine and patients with prior migraine treatment failures.
METHODS: We searched randomized clinical trials on PUBMED, EMBASE database, and Cochrane Library database. A pair-wise meta-analysis and Bayesian network analysis were performed.
RESULTS: For efficacy outcomes, the network meta-analysis suggests that in comparison to erenumab 70 mg, participants who received erenumab 140 mg reported a significant decrease in monthly acute Migraine-Specific Medication Days (MSMD) and 50% increase in response rate, and erenumab was most likely to be ranked first for Monthly Migraine Days (MMD), MSMD, and 50% response rate. For safety outcomes, the network meta-analysis has found no significant difference between the 70 mg group and the 140 mg group measured by adverse events and serious adverse events. In the 140 mg erenumab group, a significant decreased in MMD and MSMD and 50% and 75% increased in response rate were reported in patients with ≥ 2 treatment failures compared to placebo. For safety outcomes, no significant difference was found between the 140 mg erenumab group and the placebo group.
CONCLUSION: Erenumab was effective in patients with episodic migraine. A total of 140 mg erenumab was associated with better efficacy outcomes without any increased risk for developing adverse events compared to 70 mg erenumab. Furthermore, 140 mg erenumab was effective in patients with prior migraine treatment failures. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

INTRODUCTION

Migraine is one of the most common neurological disorders, with an estimated global prevalence of 15% [1]. It is manifested with recurrent attacks of unilateral, pulsatile headache that could be triggered by daily activities. A migraine attack usually lasts for 4 to 72 hours and is frequently accompanied by nausea, vomiting, photophobia, and phonophobia. Thus, patients may suffer from significant disabling pain and impaired quality of life.

As an expanding understanding of migraine pathogenesis in the past decades, multiple targets have been identified for migraine therapy. Among them, Calcitonin Gene-Related Peptide (CGRP) is considered one of the most promising targets [2]. CGRP is a 37-amino acid peptide produced through alternative RNA processing of the calcitonin gene, located in the neuronal tissue, especially C sensory fibers [3]. It has two forms, αCGRP and βCGRP. αCGRP is mainly expressed in the central and peripheral nervous system, while βCGRP is primarily found in the enteric nervous system [4]. Dimerization of Calcitonin Receptor-Like Protein (CLR) and Receptor Activity-Modifying Protein1 (RAMP1) creates CGRP receptors [4], which are located in the trigeminal neurons, peripheral intracranial vascular smooth muscle cells, the brainstem, and the dura mater [5].

CGRP receptor antagonists showed efficacy in both acute and preventative treatments of migraine attacks, whereas their use was restraint considering hepatotoxicity [5]. Erenumab is an IgG2 human monoclonal antibody (mAb), which selectively binds to the CGRP receptor, and it has been approved by the Food and Drug Administration for the prevention of migraine [6]. Previous trials have shown the safety and efficacy of erenumab compared to the placebo [1], and higher efficacy of the high erenumab dose in patients with multiple prior preventive treatment failures has been suggested [7].

So far, prior studies have demonstrated that erenumab use was associated with reduced migraine frequency and improved functional outcome compared to placebo; however, no study has been performed to evaluate the dose-response relationship of erenumab for the preventive treatment of migraine. Furthermore, although the effectiveness of erenumab in patients with prior treatment failure has been demonstrated in multiple trials, no systematic approach has been used. The purpose of this study is to conduct a meta-analysis to evaluate the effectiveness and safety of different doses of erenumab in preventive treatment in patients with migraine and patients with prior preventive treatment failures.

METHODS

A meta-analysis was performed following the Preferred Reporting Items For Systematic Reviews And Meta-Analyses (PRISMA) guidelines [8]. The study was registered at PROSPERO (http://www.crd.york.ac.uk/PROSPERO; registry number: CRD42020198985).

Search Strategy

The related articles published before April 1, 2020, were searched through PUBMED, EMBASE database, and Cochrane Library database. The search terms include migraine, erenumab, AMG334, and randomized clinical trials. The full electronic search strategy is listed in Supplement .

Study Selection

The studies included in the meta-analysis met all the following criteria: 1) randomized clinical trials; 2) patients with a history of episode migraine for ≥12 months according to the International Classification of Headache Disorders; 3) using erenumab as an experimental group intervention.

Data Extraction

The extraction of data was carried out by two investigators independently. The extracted data include (1) literature information: title, author, publication time, sample size; (2) characteristic of the object of the study including region, age, sex ratio, BMI, age at migraine onset, MMD, MSMD, number of patients who have failed previous preventive migraine medication due to insufficient efficacy or (and) unacceptable tolerability; (3) interventions: the dose of erenumab included in any phase III trials; (4) outcome data: the change in MMD, MSMD at month 3, 50% response rate (the proportion of patients achieved a 50% or greater reduction in MMD from baseline) and 75% response rate (the proportion of patients achieved a 75% or greater reduction in MMD from baseline) at month 3, the change in Headache Impact Test (Hit-6) at month 3, Migraine Physical Function Impact Diary-Everyday Activities and Physical Impairment (MPFID-EA and MPFID-PI) at month 3, number of patients with Adverse Events (AE) and Serious Adverse Events (SAE) throughout the study.

Pair-Wise Meta-Analysis

We conducted a pair-wise meta-analysis to evaluate the overall safety and efficacy of erenumab compared to the placebo and the safety and efficacy of different doses of erenumab in patients with prior treatment failures. Dosages that were assessed in any phase III trials were included. The random-effects model with the Hartung-Knapp-Sidik-Jonkman method was used. Mean Difference (MD) and Risk Ratio (RR) with their 95% Confidence Intervals (CI) were used to evaluate continuous and categorical variables, respectively. The heterogeneity between the included studies was evaluated with I. R Software version 3.6.2 (R Foundation for Statistical Computing) was used to conduct the analysis.

Network Meta-Analysis

As studies with direct and indirect comparison exist across different dosage subgroups, we conducted a Bayesian network meta-analysis to compare safety and efficacy outcomes between different dosages using the gemtc package in R software (version 3.6.2). Both fixed-effects and random-effects models were generated with Markov Chain Monte-Carlo simulation for each outcome using default priors with 5000 adaptation iterations with 100,000 iterations of 4 chains. The model with the lowest deviance information criterion was used for further analysis. The potential scale reduction factor was used to assess the model convergence, using a cut-off value of 1.005. The node-split method was used for assessing inconsistency. Log Odds Ratio (LOR) and mean difference with their 95% CI were calculated for binary variables and continuous variables, respectively.

Risk of Bias

For assessing the risk of bias of RCTs, we used the standard approach developed by the Cochrane collaboration, which included: selection bias, performance bias, detection bias, attrition bias, reporting bias, and other potential biases. The risk of bias plot in individual studies was created using the Review Manager 5.3 software.

RESULTS

Baseline Characteristics

We pooled a total of 2453 patients from five randomized controlled trials to analyze the role of erenumab in episodic migraine [9-13]. Fig. () shows the PRISMA flow diagram of the study inclusion process. Characteristics of included trials are listed in Table . Among these included trials, we found two studies that reported the effect of erenumab in episodic migraineurs who had preventive treatment failures [11, 14]. The baseline characteristics of each study are shown in Table . Overall, 84.2% of patients were female. The baseline MMD of five episodic migraine studies were 8.34±2.56. Our study included the data from erenumab 70 and 140 mg groups, as these dosages were examined in the phase III trials. The risk of bias in each included trial is plotted in Fig. ().

Overall Safety and Efficacy

First, we evaluated the overall efficacy of erenumab. The pooled results showed that patients in the erenumab group achieved a greater than 50% reduction in MMD from baseline compared to the placebo group (RR: 1.63, 95% CI: 1.28 to 2.08, I2 = 30.88%) (Fig. ). Subsequently, our results found that the erenumab group had a significant reduction of MMD from baseline compared to the placebo group (MD: -1.41, 95% CI: -1.80 to -1.03, I2 = 0%) (Fig. ). Furthermore, in comparison to the placebo group, the use of erenumab was associated with a significant reduction of MSMD (MD: -1.18, 95% CI: -1.83 to -0.54) (Fig. ); considerable hetero- geneity was found (I2 = 78.12%) (Fig. ). For functional improvement, no significant difference in measured change of MPFID-EA and MPFID-PI score from baseline was found between the placebo group and the erenumab group (MD: -2.26, 95% CI: -5.50 to 0.99, I2 = 67.37%; MD: -2.00, 95% CI: -4.32 to 0.32, I2 = 40.45%, respectively) (Fig. ). However, for the HIT-6 score, patients who received erenumab reported significantly improved HIT-6 score from baseline compared to the placebo group (MD: -2.30, 95% CI: -3.41 to -1.19) (Fig. ). For the safety outcomes, no significant differences were found in adverse events (RR: 0.94, 95% CI: 0.86 to 1.03, I2 = 0%) and serious adverse events (RR: 0.79, 95% CI: 0.33 to 1.91, I2 = 0%) between the placebo and erenumab groups with low heterogeneity (Fig. ).

Network Meta-Analysis Comparing Different Doses of Erenumab

Afterwards, we conducted a Bayesian network meta-analysis assessing the safety and efficacy of different doses of erenumab for the preventive treatment of episodic migraine. In adult patients diagnosed with episodic migraine, the use of 70 mg and 140 mg erenumab was associated with significantly decreased MMD, MSMD, and 50% increased response rate compared to placebo (MMD, 70 mg, MD: -1.28, 95% CI: -1.62 to -0.95, MMD, 140 mg, MD: -1.67, 95% CI: -2.08 to -1.25; MSMD, 70 mg, MD: -0.81, 95% CI: -1 to -0.6; MSMD, 140 mg, MD: -1.32, 95% CI: -1.58 to -1.04; 50% response rate, 70 mg, LOR: 0.64, 95% CI: 0.43 to 0.85; 50% response rate, 140 mg, LOR: 0.91, 95% CI: 0.67 to 1.17) (Fig. ). Subsequently, compared to erenumab 70 mg, participants who received erenumab 140 mg reported significantly decreased MSMD and 50% increased response rate, and erenumab was most likely to be ranked first for MMD, MSMD, and 50% response rate. (MSMD, MD: -0.51, 95% CI: -0.79 to -0.23; 50% response rate, LOR: 0.28, 95% CI: 0.03 to 0.53) (Fig. ). For functional improvement, patients who received 70 mg and 140 mg erenumab reported improved MPFID-EA and MPFID-PI at month 3 (MPFID-EA, 70 mg, MD: -1.75, 95% CI: -2.52 to -0.98, MPFID-EA, 140 mg, MD: -2.63, 95% CI: -3.56 to -1.69; MPFID-PI, 70 mg, MD: -1.55, 95% CI: -2.36 to -0.74; MSMD, 140 mg, MD: -2.58, 95% CI: -3.59 to -1.58) (Fig. ). When comparing 140 mg and 70 mg, although 140 mg erenumab has a high probability to outperform 70 mg, the analysis fails to demonstrate a significant difference in MPFID-EA and MPFID-PI (MPFID-EA, MD: -0.88, 95% CI: -1.87 to 0.11; MPFID-PI, MD: -1.03, 95% CI: -2.1 to 0.03) (Fig. ). For safety outcomes, the network meta-analysis has found no significantly increased risk for patients received erenumab 70 mg and 140 mg developing adverse events and serious adverse events compared to patients who received placebo (AE, 70 mg, LOR: -0.15, 95% CI: -0.34 to 0.04; AE, 140 mg, LOR: -0.18, 95% CI: -0.4 to 0.05; SAE, 70 mg, LOR: -0.13, 95% CI: -0.9 to 0.61; SAE, 140 mg, LOR: -0.31, 95% CI: -1.2 to 0.53) (Fig. ). However, the placebo group has the highest probability to be ranked first. Furthermore, no significant difference was found between the 70 mg group and the 140 mg group measured by AE and SAE (AE, LOR: -0.03, 95% CI: -0.27 to 0.21; SAE, LOR: -0.17, 95% CI: -1.13 to 0.73) (Fig. ). Detailed rank probability chart is listed in Supplement S2, Inconsistency analysis, DIC for random and fixed model, and diagnosis for convergence of each model are listed in Supplement S3-S5.

Safety and Efficacy of Erenumab in Patients with Prior Treatment Failures

We then assessed the safety and efficacy of different doses of erenumab in patients with ≥2 treatment failures. For efficacy endpoints, patients treated with 70 mg erenumab showed no significant difference in all the pooled efficacy endpoints compared to the placebo group (MMD, MD: -0.9, 95% CI: -2.41 to 0.6; MSMD, MD: -0.1, 95% CI: 1.23 to 1.03; 50% response rate, RR: 1.79, 95% CI: 0.65 to 4.95; 75% response rate, RR: 3.86, 95% CI: 0.5 to 29.72) (Table ). Subsequently, for safety outcomes, the use of 70 mg erenumab is not associated with increased risk for developing adverse events or serious adverse events compared to placebo (adverse events, RR: 0.96, 95% CI: 0.7 to 1.31; serious adverse events, RR: 11.59, 95% CI: 0.02 to 6481.06) (Table , Supplement -11). As one study was included in the analysis, the heterogeneity could not be assessed. Then, for 140 mg erenumab, patients in the 140 mg erenumab group reported significantly reduced MMD and MSMD (MMD, MD: -1.98, 95% CI: -2.93 to -1.03; MSMD, MD: -1.68, 95% CI: -2.27 to -1.09) (Table ). As for the 50% and 75% response rate, the use of 140 mg erenumab was related to significantly increased 50% and 75% reduction in MMD from the baseline compared to placebo (50% response rate, RR: 2.39, 95% CI:1.52 to 3.77; 75% response rate, RR: 3.32, 95% CI:1.37 to 8.05) (Table ). For safety outcomes, we found no significant difference in 140 mg erenumab compared to placebo (AE, RR: 0.96, 95% CI: 0.79 to 1.15; SAE, RR: 2.66, 95% CI: 0.29 to 24.79) (Table , Supplement -17). Heterogeneity was low in all the included outcomes.

DISCUSSION

Our study pooled five randomized clinical trials evaluating the safety and efficacy of erenumab for the treatment of episodic migraine. Our analysis showed that erenumab was efficacious and safe for the treatment of migraine. Furthermore, our study pooled both direct and indirect evidence using the Bayesian network meta-analysis method and demonstrated that 140 mg erenumab outperforms 70 mg erenumab in multiple efficacy endpoints while related to the same risk for developing adverse events. In addition, our study demonstrated that 70 mg and 140 mg erenumab were associated with significantly reduced migraine frequency and improved functional outcomes in patients with prior migraine treatment failures. The heterogeneity was low across all the primary outcomes, indicating a high level of clinical evidence. It is the first meta-analysis that compares the safety and efficacy of different doses of erenumab and the first meta-analysis to demonstrate the safety and efficacy of erenumab in patients with ≥2 prior migraine treatment failures.

The origin of the mechanisms is unclear. However, the involvement of the activation of the trigeminovascular system in migraine is widely accepted. The activation of trigeminal ganglion stimulates the trigeminal nerve fibers. These nerve fibers, releasing CGRP, project to intracranial and extracranial structures, including the pial, arachnoid, dural blood vessels, and the spinal cord trigeminocervical complex (TCC) [15]. Then, the neurons from the TCC project to the brainstem and even to higher-order regions. Some interesting discoveries have been found in the past decades. Serum CGRP levels are elevated during migraine attacks [16]. Meanwhile, the infusion of human CGRP could induce headaches and migraine in migraineurs [17]. CGRP receptors are widely distributed in both the central and peripheral nervous systems [18]. During this process, CGRP is thought to be involved in the transmission of pain information [15]. Perivascular release of CGRP from the trigeminal nerve induces vasodilation, dural mast cell degranulation, and satellite glial activation, leading to peripheral sensitization. The role of CGRP in central sensitization has also been demonstrated.

Although current evidence suggests that the effectiveness of CGRP monoclonal antibodies in migraine treatment is not dramatically increased compared to traditional therapy, the monoclonal antibodies targeting CGRP and its receptors have their unique advantages in migraine treatment. Low compliance in patients with migraine with chronic prophylactic medication use is frequently reported [19]. Erenumab has been designed and modified to extend its circulating half-lives [20]. In clinical practice, it could be given once per month, which could potentially increase compliance among migraineurs. As a preventive therapy, erenumab is likely to be prescribed for long-term use. Thus, the cross-talk of erenumab with other commonly-used drugs is another concern for physicians. A study conducted in 2017 found that subcutaneous erenumab did not influence the effect of estrogen/progestin combination oral contraceptives among healthy females [21]. A placebo-controlled trial investigating co-administration of erenumab 140 mg and sumatriptan 12 mg has found no additional effect on averages of mean arterial pressure or the pharmacokinetics of sumatriptan [22]. Furthermore, evidence suggests that the long-term use of erenumab increased the conversion from chronic migraine to episode migraine [23], especially 140 mg dose [24]. Besides, a previous study reported that erenumab use was associated with a higher response rate in patients who had a high susceptibility to migraine induction by CGRP [25], which suggested its potential applicable role. Moreover, results from clinical trials have demonstrated that erenumab is effective in patients with medication overuse [26-28]. In a posthoc analysis, erenumab showed comparable efficacy between medication over-users and the non-medication overuse group [29]. A cost-analysis based on US societal perspective Markov health state transition model has demonstrated that the use of erenumab was associated with reduced migraine-related direct and indirect costs compared to supportive care [30].

As CGRP ligand could dilate blood vessels, the potential risk on the cardiovascular system caused by CGRP targeted therapies attracts much attention. A study conducted on human isolated cranial arteries has found that the use of erenumab was not associated with direct vasoconstriction and did not influence the effect of endogenous or exogenous vasoactive compounds [31]. A 12-week trial conducted by Tepper et al. confirmed that erenumab did not affect the blood pressure and 24-hour blood pressure changes in healthy volunteers [32]. No significant difference was found in the emergence of vascular adverse events between the erenumab group and the placebo group in the short-term migraine treatment phase [33]. In addition, a study conducted on patients with stable angina has found that the use of erenumab had no effect on exercise time [34]. Although these studies have demonstrated that CGRP targeted therapies are not likely to induce severe adverse events caused by vasoconstriction, CGRP may play a more critical role in the change of vascular tension in hypertensive rats than in normotensive rats [35]. Hence, future researches are still needed to evaluate the long-term use of erenumab in patients with cardiovascular risk or hypertension.

Our study mainly pooled short-term placebo-controlled trials for episodic migraineurs. Erenumab also showed its effect on chronic migraine patients [36]. So far, a limited number of studies have been conducted to evaluate the long-term use of erenumab. An open-label study evaluating long-term safety and efficacy of erenumab in patients with episodic migraine found that erenumab use is related to improved function and favorable safety and tolerability profile [37]. The long-term adverse effects of erenumab include injection-site reactions, constipation, and muscle spasm [38]. In another similar long-term study, erenumab was found to be safe and well-tolerated, and the adverse events were considered consistent with shorter-term placebo treatment [39].

Our study had a few limitations. First, although our study included five multicenter randomized trials that have a low risk for bias, the heterogeneity of overall functional improvement in the pair-wise meta-analysis was considerably high, indicating a low level of clinical evidence. Second, all the included clinical trials were limited to short-term use; further pooled analyses based on long-term, or real-world studies are needed. Third, our analysis on 70 mg erenumab in patients with previous treatment failure only includes one trial with insufficient sample size. Further studies are still needed to provide more robust evidence.

CONCLUSION

Our results showed that compared to 70mg erenumab, 140 mg erenumab might be a better choice for patients with episodic migraine, especially for those with prior migraine treatment failures. So far, no direct comparison between using 140 mg directly and switching 70 mg to 140 mg, if poorly responded, has been made. Further studies need to be carried out if possible.

Table 1

Characteristics of included studies.

Trials (NCT number)	Phase	Inclusion Criteria	Exclusion Criteria	Group*	Frequency
Publication
Center
Sakai 2019(NCT02630459)	Phase 2	1. Aged 20-65 years2. A diagnosis of migraine as defined by ICHD-III beta for at least 1 year prior3. A history of 4-15 headache days per month on average across the three months prior to screening	1. Over 50 years old at migraine onset2. History of cluster headache or hemiplegic migraine3. Failure to respond to three or more classes of migraine preventive treatments4. Receiving botulinum toxin within four months before screening5. The use of interventions or devices for migraine during the two months prior to screening6. Receiving more than 1 migraine-preventive medication	Erenumab 28 mgErenumab 70 mgErenumab 140 mgPlacebo	Once a month for 6 months
Headache
Multicenter
Dodick 2018(NCT02483585)	Phase 3	1. Aged 18-65 years2. A history of 4-15 migraine days per month and < 15 headache days per month for at least one year prior	1. Over 50 years old at migraine onset2. History of cluster headache or hemiplegic migraineReceiving botulinum toxin within four months before screening	Erenumab 70 mg	Once a month for 3 months
				Placebo
Cephalalgia
Multicenter
Reuter 2018(NCT03096834)	Phase 3	1. Aged 18-65 years2. A diagnosis of migraine as defined by ICHD-III beta for at least one year prior3. A history of 4-14 headache days per month on average across the three months prior to screening4. Have previously been treated unsuccessfully	1. Over 50 years old at migraine onset2. History of cluster headache or hemiplegic migraine3. Use a preventive migraine medication within five times the drug’s half-life before baseline4. Receiving botulinum toxin within four months before screening5. The use of interventions or devices for migraine within the month prior to screening	Erenumab 140 mg	Once a month for 3 months
				Placebo
Lancet
Multicenter
Goadsby 2017(NCT02456740)	Phase 3	1. Aged 18-65 years2. A diagnosis of migraine as defined by ICHD-III beta for at least one year prior3. A history of 4-15 migraine days per month and < 15 headache days per month for at least three months prior	1. Over 50 years old at migraine onset2. History of cluster headache or hemiplegic migraine3. Receiving botulinum toxin within four months before screening4. The use of interventions or devices for migraine within two months prior to screening	Erenumab 70 mgErenumab 140 mgPlacebo	Once a month for 6 months
New England Journal of Medicine
Multicenter
Sun 2016(NCT01952574)	Phase 2	1. Aged 18-60 years2. A diagnosis of migraine as defined by ICHD-II for at least one year prior3. A history of 4-14 migraine days per month and < 15 headache days per month for at least three months prior	1. Over 50 years old at migraine onset2. History of cluster headache or hemiplegic migraine3. Overuse of acute treatment for headache4. Receiving more than 1 migraine-preventive medication during the two months prior to screening5. Receiving botulinum toxin within six months before screening	Erenumab 7 mgErenumab 21 mgErenumab 70 mgPlacebo	Once a month for 3 months
Lancet Neurology
Multicenter

* We only collected data from patients who received >=70mg erenumab.

Table 2

Baseline characteristics of included patients.

Trials	Region	Treatment	Populations	Age (SD)	Female Sex (%)	BMI (SD)	Age at onset (SD)	MMD (SD)	MSMD (SD)	Failed Previous Migraine-Preventive Medications
Sakai 2019	Japan	Erenumab 70 mg	135	44(NA)	115(85.2%)	21.6(3.5)	NA	7.8(2.3)	5.4(2.9)	43
		Erenumab 140 mg	137	45(NA)	112(81.8%)	22(3.5)	NA	8.1(2.4)	5.9(2.9)	54
		Placebo	136	45(NA)	118(86.8%)	22.1(3.5)	NA	7.7(2.3)	5.6(2.5)	44
Dodick 2018	North America and Europe	Erenumab 70 mg	286	42(11)	245(85.7%)	27.4(6.3)	21(10)	8.1(2.7)	3.7(3.6)	117
		Placebo	291	42(12)	247(84.9%)	27.4(6.1)	22(11)	8.4(2.6)	3.4(3.6)	115
Goadsby 2017	North America, Europe and Turkey	Erenumab 70 mg	317	41.1(11.3)	268(84.5%)	27.3(5.9)	21.4(11)	8.3(2.5)	3.2(3.4)	127
		Erenumab 140 mg	319	40.4(11.1)	272(85.3%)	27(6.2)	20.7(9.9)	8.3(2.5)	3.4(3.5)	116
		Placebo	319	41.3(11.2)	274(85.9%)	27.1(6.3)	21.2(10.2)	8.2(2.5)	3.4(3.4)	127
Sun 2016	North America and Europe	Erenumab 70 mg	107	42.6(9.9)	82(76.6%)	25.8(4.9)	21.7(11.7)	8.6(2.5)	4.3(3.5)	34
		Placebo	160	41.4(10)	132(82.5%)	25.9(4.9)	20.7(11.5)	8.8(2.7)	4.5(3.9)	60
Reuter 2018	Europe and Australia	Erenumab 140 mg	121	44.6(10.5)	97(80.2)	25(4.2)	NA	9.2(2.6)	4.8(2.9)	121
		Placebo	125	44.2(10.6)	103(82.4%)	24.9(5.1)	NA	9.3(2.7)	4.4(2.8)	125

NA=not applicable; BMI=Body Mass Index; MMD=Monthly Migraine Days; MSMD=Monthly Acute Migraine-Specific Medication Treatment Days.

Table 3

Efficacy and safety of 70mg erenumab in patients with ≥ 2 prior treatment failures.

Outcomes	Erenumab 70 mg Group (n=49)	Placebo Group (n=27)	Number of Trials Included (Total Patients)	Combined Risk Ratio or Mean Difference (95% CI)	I2
MMD	-1.8 (3.09), n=49	-0.9 (3.29), n=27	1 (n=76)	-0.9 (-2.41 to 0.61) #	NA
MSMD	-1.1 (2.46), n=49	-1 (2.38), n=27	1 (n=76)	-0.1 (-1.23 to 1.03) #	NA
50% response rate	13/49 (26.53%)	4/27 (14.81%)	1 (n=76)	1.79 (0.65 to 4.95) *	NA
75% response rate	7/49 (14.29%)	1/27 (3.7%)	1 (n=76)	3.86 (0.5 to 29.72) *	NA
AE	33/49 (67.35%)	19/27 (70.37%)	1 (n=76)	0.96 (0.7 to 1.31) *	NA
SAE	2/49 (4.08%)	0/27 (0%)	1 (n=76)	11.59 (0.02 to 6481.06) *	NA

Outcome data are mean (SD) or n/N (%). NA= not applicable; MMD=Monthly Migraine Days; MSMD=Monthly Acute Migraine-Specific Medication Treatment Days; AE=Adverse Events; SAE=Serious Adverse Events; CI=Confidence Interval. *Risk ratio (binary outcomes). #Mean difference (quantitative outcomes).

Table 4

Efficacy and safety of 140mg erenumab in patients with ≥ 2 prior treatment failures.

Outcomes	Erenumab 140 mg Group (n=177)	Placebo Group (n=151)	Number of Trials Included (Total Patients)	Combined Risk Ratio or Mean Difference (95% CI)	I2
MMD	-2.36 (4.05), n=176	-0.33 (4.2), n=147	2 (n=323)	-1.98 (-2.93 to -1.03) #	11.43
MSMD	-1.66 (2.3), n=176	0.22 (3.19), n=147	2 (n=323)	-1.68 (-2.27 to -1.09) #	0
50% response rate	63/177 (35.59%)	21/151 (13.91%)	2 (n=328)	2.39 (1.52 to 3.77) *	0
75% response rate	26/177 (14.69%)	6/151 (3.97%)	2 (n=328)	3.32 (1.37 to 8.05) *	0
AE	100/177 (56.5%)	86/151 (56.95%)	2 (n=328)	0.96 (0.79 to 1.15) *	0
SAE	5/177 (2.82%)	1/151 (0.66%)	2 (n=328)	2.66 (0.29 to 24.79) *	0

Outcome data are mean (SD) or n/N (%). NA= not applicable; MMD=Monthly Migraine Days; MSMD=Monthly Acute Migraine-Specific Medication Treatment Days; AE=Adverse Events; SAE=Serious Adverse Events; CI=Confidence Interval. *Risk ratio (binary outcomes). #Mean difference (quantitative outcomes).