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

Biological therapy meta-analysis migraine monoclonal antibody neurology systematic review

Journal

European journal of pharmacology
ISSN: 1879-0712
Titre abrégé: Eur J Pharmacol
Pays: Netherlands
ID NLM: 1254354

Informations de publication

Date de publication:
30 May 2024
Historique:
received: 12 02 2024
revised: 04 05 2024
accepted: 29 05 2024
medline: 2 6 2024
pubmed: 2 6 2024
entrez: 1 6 2024
Statut: aheadofprint

Résumé

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

Sections du résumé

BACKGROUND 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 OBJECTIVE
To assess the clinical effectiveness and safety of erenumab for reducing migraine intensity and frequency in the real world.
METHODS 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 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 CONCLUSIONS
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.

Identifiants

pubmed: 38823758
pii: S0014-2999(24)00390-X
doi: 10.1016/j.ejphar.2024.176702
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

176702

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare no conflicts of interest.

Auteurs

Jaime Fernández-Bravo-Rodrigo (J)

Health and Social Research Center, Universidad de Castilla-La Mancha, Cuenca 16071, Spain; Pharmacy Service, Hospital Virgen de la Luz, 16002 Cuenca, Spain; Pharmacy Service. Hospital Virgen del Castillo, 30510 Yecla, Murcia, Spain. Electronic address: jaime.fernandezbravo@alu.uclm.es.

Iván Cavero-Redondo (I)

Facultad de Ciencias de la Salud, Universidad Autónoma de Chile, Talca 3460000, Chile. Electronic address: ivan.cavero@uclm.es.

Maribel Lucerón-Lucas-Torres (M)

Health and Social Research Center, Universidad de Castilla-La Mancha, Cuenca 16071, Spain. Electronic address: mariaisabel.luceron@uclm.es.

Irene Martínez-García (I)

Health and Social Research Center, Universidad de Castilla-La Mancha, Cuenca 16071, Spain. Electronic address: irene.mgarcia@uclm.es.

Amparo Flor-García (A)

Pharmacy Service, Hospital Virgen de la Luz, 16002 Cuenca, Spain. Electronic address: amparof@sescam.jccm.es.

Dolores Barreda-Hernández (D)

Pharmacy Service, Hospital Virgen de la Luz, 16002 Cuenca, Spain. Electronic address: dbarreda@sescam.org.

Carlos Pascual-Morena (C)

Health and Social Research Center, Universidad de Castilla-La Mancha, Cuenca 16071, Spain; Facultad de Enfermería de Albacete, Universidad de Castilla-La Mancha, Albacete 02006, Spain. Electronic address: carlos.pascual@uclm.es.

Classifications MeSH