TY - JOUR
T1 - Combining treatments for migraine prophylaxis
T2 - the state-of-the-art
AU - Pellesi, Lanfranco
AU - Garcia-Azorin, David
AU - Rubio-Beltrán, Eloisa
AU - Ha, Wook Seok
AU - Messina, Roberta
AU - Ornello, Raffaele
AU - Petrusic, Igor
AU - Raffaelli, Bianca
AU - Labastida-Ramirez, Alejandro
AU - Ruscheweyh, Ruth
AU - Tana, Claudio
AU - Vuralli, Doga
AU - Waliszewska-Prosół, Marta
AU - Wang, Wei
AU - Wells-Gatnik, William
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/12
Y1 - 2024/12
N2 - 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.
AB - 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.
KW - CGRP
KW - Gepants
KW - Onabotulinumtoxin A
KW - Propranolol
KW - Rational polytherapy
KW - Topiramate
UR - https://www.scopus.com/pages/publications/85211385604
U2 - 10.1186/s10194-024-01925-w
DO - 10.1186/s10194-024-01925-w
M3 - Review article
C2 - 39639191
AN - SCOPUS:85211385604
SN - 1129-2369
VL - 25
JO - Journal of Headache and Pain
JF - Journal of Headache and Pain
IS - 1
M1 - 214
ER -