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Combining treatments for migraine prophylaxis: the state-of-the-art

Authors
 Lanfranco Pellesi  ;  David Garcia-Azorin  ;  Eloisa Rubio-Beltrán  ;  Wook-Seok Ha  ;  Roberta Messina  ;  Raffaele Ornello  ;  Igor Petrusic  ;  Bianca Raffaelli  ;  Alejandro Labastida-Ramirez  ;  Ruth Ruscheweyh  ;  Claudio Tana  ;  Doga Vuralli  ;  Marta Waliszewska-Prosół 18  ;  Wei Wang  ;  William Wells-Gatnik 
Citation
 JOURNAL OF HEADACHE AND PAIN, Vol.25(1) : 214, 2024-12 
Journal Title
JOURNAL OF HEADACHE AND PAIN
ISSN
 1129-2369 
Issue Date
2024-12
MeSH
Antibodies, Monoclonal / therapeutic use ; Botulinum Toxins, Type A* / administration & dosage ; Botulinum Toxins, Type A* / therapeutic use ; Calcitonin Gene-Related Peptide / antagonists & inhibitors ; Calcitonin Gene-Related Peptide / immunology ; Calcitonin Gene-Related Peptide Receptor Antagonists* / therapeutic use ; Drug Therapy, Combination ; Humans ; Migraine Disorders* / drug therapy ; Migraine Disorders* / prevention & control
Keywords
CGRP ; Gepants ; Onabotulinumtoxin A ; Propranolol ; Rational polytherapy ; Topiramate
Abstract
Combination treatments for migraine prophylaxis present a promising approach to addressing the diverse and complex mechanisms underlying migraine. This review explores the potential of combining oral conventional prophylactics, onabotulinumtoxin A, monoclonal antibodies (mAbs) targeting the calcitonin gene-related peptide (CGRP) pathway, and small molecule CGRP receptor antagonists (gepants). Among the most promising strategies, dual CGRP inhibition through mAbs and gepants may enhance efficacy by targeting both the CGRP peptide and its receptor, while the combination of onabotulinumtoxin A with CGRP treatments offers synergistic pain relief. Oral non-CGRP treatments, which are accessible and often prescribed for patients with comorbid conditions, provide an affordable and practical option in combination regimens. Despite the potential of these combinations, there is a lack of evidence to support their widespread inclusion in clinical guidelines. The high cost of certain combinations, such as onabotulinumtoxin A with a CGRP mAb or dual anti-CGRP mAbs, presents feasibility challenges. Further large-scale trials are needed to establish safe and effective combination protocols and solidify their role in clinical practice, particularly for treatment-resistant patients.
Files in This Item:
T202502897.pdf Download
DOI
10.1186/s10194-024-01925-w
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers
Yonsei Authors
Ha, Woo Seok(하우석) ORCID logo https://orcid.org/0000-0003-1188-449X
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/206549
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