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

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          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.

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          Most cited references162

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          A Controlled Trial of Erenumab for Episodic Migraine

          We tested erenumab, a fully human monoclonal antibody that inhibits the calcitonin gene-related peptide receptor, for the prevention of episodic migraine.
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            Galcanezumab in chronic migraine

            Objective To evaluate the efficacy and safety of galcanezumab, a humanized monoclonal antibody that selectively binds to calcitonin gene-related peptide, in the preventive treatment of chronic migraine. Methods A phase 3, randomized, double-blind, placebo-controlled study of LY2951742 in patients with chronic migraine (Evaluation of Galcanezumab in the Prevention of Chronic Migraine [REGAIN]) was a phase 3 study with a 3-month double-blind, placebo-controlled treatment phase and a 9-month open-label extension. Eligible patients 18 to 65 years of age with chronic migraine were randomized 2:1:1 to monthly subcutaneous injections of placebo (n = 558), galcanezumab 120 mg (with a 240-mg loading dose, n = 278), or galcanezumab 240 mg (n = 277). The primary endpoint was the overall mean change from baseline in the number of monthly migraine headache days (MHDs) during the 3-month double-blind treatment phase. Results Mean number of monthly MHDs at baseline was 19.4 for the total sample. Both galcanezumab dose groups demonstrated greater overall mean reduction in the number of monthly MHDs compared to placebo (placebo −2.7, galcanezumab 120 mg −4.8, galcanezumab 240 mg −4.6) (p < 0.001 for each dose compared to placebo). There were no clinically meaningful differences between galcanezumab doses and placebo on any safety or tolerability outcome except for a higher incidence of treatment-emergent injection-site reaction (p < 0.01), injection-site erythema (p < 0.001), injection-site pruritus (p < 0.01), and sinusitis (p < 0.05) in the galcanezumab 240-mg group relative to placebo. Conclusions Both doses of galcanezumab were superior to placebo in reducing the number of monthly MHDs. Galcanezumab appears efficacious, safe, and well tolerated for the preventive treatment of chronic migraine. ClinicalTrials.gov identifier NCT02614261. Classification of evidence This interventional study provides Class I evidence that galcanezumab is superior to placebo in the reduction of the number of monthly MHDs.
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              Fremanezumab for the Preventive Treatment of Chronic Migraine

              Fremanezumab, a humanized monoclonal antibody targeting calcitonin gene-related peptide (CGRP), is being investigated as a preventive treatment for migraine. We compared two fremanezumab dose regimens with placebo for the prevention of chronic migraine.
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                Author and article information

                Contributors
                lpellesi@health.sdu.dk
                Journal
                J Headache Pain
                J Headache Pain
                The Journal of Headache and Pain
                Springer Milan (Milan )
                1129-2369
                1129-2377
                5 December 2024
                5 December 2024
                2024
                : 25
                : 1
                : 214
                Affiliations
                [1 ]Department of Public Health, Clinical Pharmacology, Pharmacy and Environmental Medicine, University of Southern Denmark, ( https://ror.org/03yrrjy16) Campusvej 55, Odense, 5230 Denmark
                [2 ]Department of Medicine, Toxicology and Dermatology, Faculty of Medicine, University of Valladolid, ( https://ror.org/01fvbaw18) Valladolid, Spain
                [3 ]Department of Neurology, Hospital Universitario Río Hortega, ( https://ror.org/05jk45963) Valladolid, Spain
                [4 ]Headache Group, Wolfson Sensory, Pain and Regeneration Centre, Institute of Psychiatry, Psychology and Neuroscience, King’s College London, ( https://ror.org/0220mzb33) London, United Kingdom
                [5 ]Department of Neurology, Yonsei University College of Medicine, ( https://ror.org/01wjejq96) Seoul, Korea
                [6 ]GRID grid.18887.3e, ISNI 0000000417581884, Neuroimaging Research Unit and Neurology Unit, , IRCCS San Raffaele Scientific Institute, ; Milan, Italy
                [7 ]Vita-Salute San Raffaele University, ( https://ror.org/01gmqr298) Milan, Italy
                [8 ]Department of Biotechnological and Applied Clinical Sciences, University of L’Aquila, ( https://ror.org/01j9p1r26) L’Aquila, Italy
                [9 ]Laboratory for Advanced Analysis of Neuroimages, Faculty of Physical Chemistry, University of Belgrade, ( https://ror.org/02qsmb048) Belgrade, Serbia
                [10 ]GRID grid.6363.0, ISNI 0000 0001 2218 4662, Department of Neurology, , Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, ; Berlin, Germany
                [11 ]Clinician Scientist Program, Berlin Institute of Health (BIH) at Charité – Universitätsmedizin Berlin, ( https://ror.org/001w7jn25) Berlin, Germany
                [12 ]Division of Neuroscience, Faculty of Biology, Medicine, and Health, University of Manchester, ( https://ror.org/027m9bs27) Manchester, United Kingdom
                [13 ]GRID grid.5252.0, ISNI 0000 0004 1936 973X, Department of Neurology, , LMU University Hospital, LMU Munich, ; Munich, Germany
                [14 ]Center of Excellence on Headache, Geriatrics Clinic, Ss. Annunziata of Chieti, Italy
                [15 ]Department of Neurology and Algology, Faculty of Medicine, Gazi University, ( https://ror.org/054xkpr46) Ankara, Türkiye
                [16 ]Neuropsychiatry Center, Gazi University, ( https://ror.org/054xkpr46) Ankara, Türkiye
                [17 ]Neuroscience and Neurotechnology Center of Excellence (NÖROM), Gazi University, ( https://ror.org/054xkpr46) Ankara, Türkiye
                [18 ]Department of Neurology, Wroclaw Medical University, ( https://ror.org/01qpw1b93) Wroclaw, Poland
                [19 ]GRID grid.13402.34, ISNI 0000 0004 1759 700X, Department of Neurology, Sir Run Run Shaw Hospital, School of Medicine, , Zhejiang University, ; Hangzhou, China
                [20 ]Department of Neurology, Headache Center, Beijing Tiantan Hospital, Capital Medical University, ( https://ror.org/013xs5b60) Beijing, China
                [21 ]Department of Clinical and Molecular Medicine, Sapienza University, ( https://ror.org/02be6w209) Rome, Italy
                Article
                1925
                10.1186/s10194-024-01925-w
                11619619
                39639191
                d728f822-b4f5-40c2-801b-c12824bc3c6c
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

                History
                : 1 November 2024
                : 22 November 2024
                Categories
                Review
                Custom metadata
                © Springer-Verlag Italia S.r.l., part of Springer Nature 2024

                Anesthesiology & Pain management
                cgrp,gepants,onabotulinumtoxin a,propranolol,rational polytherapy,topiramate

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