CGRP monoclonal antibodies in migraine: an efficacy and tolerability comparison with standard prophylactic drugs.

Calcitonin gene-related peptide Chronic migraine Episodic migraine Migraine Monoclonal antibody Preventive treatment

Journal

The journal of headache and pain
ISSN: 1129-2377
Titre abrégé: J Headache Pain
Pays: England
ID NLM: 100940562

Informations de publication

Date de publication:
25 Oct 2021
Historique:
received: 13 07 2021
accepted: 24 09 2021
entrez: 26 10 2021
pubmed: 27 10 2021
medline: 28 10 2021
Statut: epublish

Résumé

Several drugs are available for the preventive treatment of both episodic and chronic migraine. The choice of which therapy to initiate first, second, or third is not straightforward and is based on multiple factors, including general efficacy, tolerability, potential for serious adverse events, comorbid conditions, and costs. Recently, a new class of migraine preventive drugs was introduced, i.e. monoclonal antibodies against calcitonin gene-related peptide (CGRP) or its receptor. The present article summarizes the evidence gathered with this new migraine preventive drug class from randomized placebo-controlled clinical trials. It further puts this into perspective next to the evidence gained by the most widely used agents for the prevention of episodic and chronic migraine with an emphasis on efficacy and the robustness with which this efficacy signal was obtained. Although being a relatively new class of migraine preventive drugs, monoclonal antibodies blocking the CGRP pathway have an efficacy which is at least comparable if not higher than those of the currently used preventive drugs. Moreover, the robustness of this efficacy signal is substantiated by several randomized clinical trials each including large numbers of patients. In addition, because of their excellent tolerability and with long-term safety data emerging, they seem to have an unprecedented efficacy over adverse effect profile, clearly resulting in an added value for migraine prevention. Balancing the data presented in the current manuscript with additional data concerning long term safety on the one hand and cost issues on the other hand, can be of particular use to health policy makers to implement this new drug class in the prevention of migraine.

Sections du résumé

BACKGROUND BACKGROUND
Several drugs are available for the preventive treatment of both episodic and chronic migraine. The choice of which therapy to initiate first, second, or third is not straightforward and is based on multiple factors, including general efficacy, tolerability, potential for serious adverse events, comorbid conditions, and costs. Recently, a new class of migraine preventive drugs was introduced, i.e. monoclonal antibodies against calcitonin gene-related peptide (CGRP) or its receptor.
METHODS METHODS
The present article summarizes the evidence gathered with this new migraine preventive drug class from randomized placebo-controlled clinical trials. It further puts this into perspective next to the evidence gained by the most widely used agents for the prevention of episodic and chronic migraine with an emphasis on efficacy and the robustness with which this efficacy signal was obtained.
RESULTS RESULTS
Although being a relatively new class of migraine preventive drugs, monoclonal antibodies blocking the CGRP pathway have an efficacy which is at least comparable if not higher than those of the currently used preventive drugs. Moreover, the robustness of this efficacy signal is substantiated by several randomized clinical trials each including large numbers of patients. In addition, because of their excellent tolerability and with long-term safety data emerging, they seem to have an unprecedented efficacy over adverse effect profile, clearly resulting in an added value for migraine prevention.
CONCLUSIONS CONCLUSIONS
Balancing the data presented in the current manuscript with additional data concerning long term safety on the one hand and cost issues on the other hand, can be of particular use to health policy makers to implement this new drug class in the prevention of migraine.

Identifiants

pubmed: 34696711
doi: 10.1186/s10194-021-01335-2
pii: 10.1186/s10194-021-01335-2
pmc: PMC8547103
doi:

Substances chimiques

Antibodies, Monoclonal 0
Pharmaceutical Preparations 0
Calcitonin 9007-12-9
Calcitonin Gene-Related Peptide JHB2QIZ69Z

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

128

Informations de copyright

© 2021. The Author(s).

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Auteurs

Fenne Vandervorst (F)

Department of Neurology, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium.

Laura Van Deun (L)

Department of Neurology, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium.

Annelies Van Dycke (A)

Department of Neurology, General Hospital Sint-Jan Bruges, Bruges, Belgium.

Koen Paemeleire (K)

Department of Neurology, Ghent University Hospital, Ghent, Belgium.

Uwe Reuter (U)

Department of Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Jean Schoenen (J)

Headache Research Unit, Dept of Neurology-Citadelle Hospital, University of Liège, Liège, Belgium.

Jan Versijpt (J)

Department of Neurology, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium. jan.versijpt@uzbrussel.be.

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Classifications MeSH