Abstract

BackgroundMigraine is one of the leading causes of disability worldwide. Erenumab is a fully human monoclonal antibody that targets the calcitonin gene-related peptide (CGRP) receptor. This study aimed to evaluate real-world evidence on the impact of erenumab on acute medication usage and health care resource utilization (HCRU) among migraine patients.MethodsThis retrospective effectiveness study utilized the US Optum’s de-identified Clinformatics® Data Mart database to identify migraine patients initiating erenumab between May 1, 2018 and September 30, 2019. Patients had to be at least 18 years old, with a minimum of three doses for erenumab in the 6-month post-index period and continuous medical/pharmacy coverage in the 12-month pre- and 6-month post-index period. The date of the first claim for erenumab served as the index date. Use of acute medications overall and at different drug class level, and HCRU were compared during the 6-month pre- vs. post-index period. Impact of erenumab on a composite endpoint of three possible events: 1) outpatient visit with a diagnosis of migraine and an associated acute medication claim within 7 days of the visit, 2) hospital admission with a primary diagnosis for migraine, or 3) emergency room visit with a primary diagnosis for migraine (any events that occurred ≤3 days apart were counted only once) was also evaluated.ResultsThe analysis included 3171 identified patients. At 6 months, following initiation of erenumab, acute medication use including the number of types of acute medication, number of claims of each medication and % of patients who received acute medication, and HCRU were significantly decreased. For the composite outcome, the mean number of events decreased from 1.03 to 0.77 (rate ratio: 0.75; 95% CI: 0.71 to 0.79; P < 0.0001). A decrease in the proportion of patients with any of the three events was also observed (52.7% vs. 39.5%, P < 0.0001).ConclusionIn this retrospective analysis, erenumab was associated with significantly reduced acute medication use and HCRU in a real-world setting, hence significantly reducing the burden of the disease. A composite endpoint could be used as a proxy to evaluate the burden of migraine attacks; however, further research is needed.

Highlights

  • Migraine is one of the leading causes of disability worldwide

  • This study was conducted in accordance with the Guidelines for Good Pharmacoepidemiology Practices (GPP) of the International Society for Pharmacoepidemiology (ISPE) 2016, the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guidelines, and with the ethical principles laid down in the Declaration of Helsinki

  • We present a look at the real-world effectiveness of a first-in-class anti-calcitonin gene-related peptide (CGRP) agent approved for the prevention of migraine, on acute medication usage, health care resource utilization (HCRU), and a composite endpoint reflecting the overall burden of migraine

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Summary

Introduction

Migraine is one of the leading causes of disability worldwide. Erenumab is a fully human monoclonal antibody that targets the calcitonin gene-related peptide (CGRP) receptor. This study aimed to evaluate real-world evidence on the impact of erenumab on acute medication usage and health care resource utilization (HCRU) among migraine patients. Migraine is a common neurological disorder characterized by recurrent attacks of moderate–to–severe headaches and accompanying symptoms (nausea, vomiting, and sensitivity to light, sound, or smell), and is one of the leading causes of disability worldwide [1, 2]. Pharmacologic treatment of migraine involves both acute and preventive therapy [4,5,6]. Preventive therapies aim to reduce the frequency, severity, duration of attacks, and the impact on quality of life of future migraine headaches. Preventive medications include beta blockers, anticonvulsants, antidepressants, onabotulinumtoxinA (onabotA) injection therapy, and anti-calcitonin gene-related peptide (CGRP) monoclonal antibody (mAb) drugs [8]. Preventive treatment has involved the use of medications, originally developed for other conditions [9], and oral versions have been subject to poor adherence, mainly due to suboptimal efficacy and tolerability [10,11,12]

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