Real-world effectiveness and safety of erenumab for the treatment of migraine: A systematic review and meta-analysis

Eur J Pharmacol. 2024 Aug 5:976:176702. doi: 10.1016/j.ejphar.2024.176702. Epub 2024 May 31.

Abstract

Background: Migraine is a common and disabling primary headache disorder. Several drugs targeting calcitonin gene-related peptide (CGRP), such as erenumab (an anti-CGRP receptor mAb), have been developed recently. However, the real-world effects of erenumab are not well understood.

Objective: To assess the clinical effectiveness and safety of erenumab for reducing migraine intensity and frequency in the real world.

Methods: A systematic search of PubMed, Scopus, Web of Science and the Cochrane Library was conducted from inception to December 2023. Studies estimating the real-world effect of erenumab on monthly migraine days (MMD), monthly headache days (MHD), headache impact test (HIT-6), number of days in medication (NDM), acute monthly intake (AMI), pain intensity (PI) and safety outcomes were included. Meta-analyses of proportions or mean differences were performed.

Results: Fifty-three studies were included. At 3-months, the effect was -7.18 days for MMD, -6.89 days for MHD, -6.97 for HIT-6, -6.22 days for NDM, -15.75 for AMI, and -1.71 for PI. Generally, the effect at 6- and 12-months increased slightly and gradually. The MMD/MHD response rates revealed that approximately one-third of patients exhibited a response greater than 30%, while one-sixth demonstrated a response exceeding 50%. Additionally, 3-4% of patients achieved a response rate of 100%. Adverse event rates were 0.34 and 0.43 at 6- and 12-months, respectively.

Conclusion: This study provides strong evidence of the effectiveness and safety of erenumab in the real world; to our knowledge, this is the first real-world meta-analysis specific to erenumab. Erenumab represents a solid therapeutic option for physicians.

Keywords: Biological therapy; Meta-analysis; Migraine; Monoclonal antibody; Neurology; Systematic review.

Publication types

  • Systematic Review
  • Meta-Analysis

MeSH terms

  • Antibodies, Monoclonal, Humanized* / adverse effects
  • Antibodies, Monoclonal, Humanized* / therapeutic use
  • Calcitonin Gene-Related Peptide Receptor Antagonists* / adverse effects
  • Calcitonin Gene-Related Peptide Receptor Antagonists* / pharmacology
  • Calcitonin Gene-Related Peptide Receptor Antagonists* / therapeutic use
  • Humans
  • Migraine Disorders* / drug therapy
  • Treatment Outcome

Substances

  • erenumab
  • Antibodies, Monoclonal, Humanized
  • Calcitonin Gene-Related Peptide Receptor Antagonists