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Pooled Analysis of Real-World Evidence Supports Anti-CGRP mAbs and OnabotulinumtoxinA Combined Trial in Chronic Migraine

OnabotulinumtoxinA, targeting the CGRP machinery, has been approved for the last two decades for chronic migraine prevention. The recently approved monoclonal antibodies (mAbs) directed towards the calcitonin gene-related peptide (CGRP) pathway open a new age for chronic migraine control. However, s...

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Autores principales: Scuteri, Damiana, Tonin, Paolo, Nicotera, Pierluigi, Vulnera, Marilù, Altieri, Giuseppina Cristina, Tarsitano, Assunta, Bagetta, Giacinto, Corasaniti, Maria Tiziana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9413678/
https://www.ncbi.nlm.nih.gov/pubmed/36006191
http://dx.doi.org/10.3390/toxins14080529
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author Scuteri, Damiana
Tonin, Paolo
Nicotera, Pierluigi
Vulnera, Marilù
Altieri, Giuseppina Cristina
Tarsitano, Assunta
Bagetta, Giacinto
Corasaniti, Maria Tiziana
author_facet Scuteri, Damiana
Tonin, Paolo
Nicotera, Pierluigi
Vulnera, Marilù
Altieri, Giuseppina Cristina
Tarsitano, Assunta
Bagetta, Giacinto
Corasaniti, Maria Tiziana
author_sort Scuteri, Damiana
collection PubMed
description OnabotulinumtoxinA, targeting the CGRP machinery, has been approved for the last two decades for chronic migraine prevention. The recently approved monoclonal antibodies (mAbs) directed towards the calcitonin gene-related peptide (CGRP) pathway open a new age for chronic migraine control. However, some 40% patients suffering from chronic migraine is still resistant to treatment. The aim of this work is to answer the following PICOS (participants intervention comparator outcome study design) question: Is there evidence of efficacy and safety of the combined administration of anti-CGRP mAbs and onabotulinumtoxinA in chronic migraine? A systematic review and meta-analysis [Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 recommendations] was made up to 19 April 2022. The results are encouraging: the combined treatment proved to afford ≥50% monthly headache days (MHDs)/frequency reduction respect to baseline in up to 58.8% of patients; in comparison, anti-CGRP mAbs reduce MHDs of 1.94 days from baseline and botulinum toxin of 1.86 days. Our study demonstrates for the first time that the combination therapy of onabotulinumtoxinA with anti-CGRP mAbs affords a reduction of 2.67 MHDs with respect to onabotulinumtoxinA alone, with moderate certainty of evidence. Adequately powered, good-quality studies are needed to confirm the response to combination therapy in terms of efficacy and safety. PROSPERO registration: CRD42022313640.
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spelling pubmed-94136782022-08-27 Pooled Analysis of Real-World Evidence Supports Anti-CGRP mAbs and OnabotulinumtoxinA Combined Trial in Chronic Migraine Scuteri, Damiana Tonin, Paolo Nicotera, Pierluigi Vulnera, Marilù Altieri, Giuseppina Cristina Tarsitano, Assunta Bagetta, Giacinto Corasaniti, Maria Tiziana Toxins (Basel) Article OnabotulinumtoxinA, targeting the CGRP machinery, has been approved for the last two decades for chronic migraine prevention. The recently approved monoclonal antibodies (mAbs) directed towards the calcitonin gene-related peptide (CGRP) pathway open a new age for chronic migraine control. However, some 40% patients suffering from chronic migraine is still resistant to treatment. The aim of this work is to answer the following PICOS (participants intervention comparator outcome study design) question: Is there evidence of efficacy and safety of the combined administration of anti-CGRP mAbs and onabotulinumtoxinA in chronic migraine? A systematic review and meta-analysis [Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 recommendations] was made up to 19 April 2022. The results are encouraging: the combined treatment proved to afford ≥50% monthly headache days (MHDs)/frequency reduction respect to baseline in up to 58.8% of patients; in comparison, anti-CGRP mAbs reduce MHDs of 1.94 days from baseline and botulinum toxin of 1.86 days. Our study demonstrates for the first time that the combination therapy of onabotulinumtoxinA with anti-CGRP mAbs affords a reduction of 2.67 MHDs with respect to onabotulinumtoxinA alone, with moderate certainty of evidence. Adequately powered, good-quality studies are needed to confirm the response to combination therapy in terms of efficacy and safety. PROSPERO registration: CRD42022313640. MDPI 2022-08-01 /pmc/articles/PMC9413678/ /pubmed/36006191 http://dx.doi.org/10.3390/toxins14080529 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Scuteri, Damiana
Tonin, Paolo
Nicotera, Pierluigi
Vulnera, Marilù
Altieri, Giuseppina Cristina
Tarsitano, Assunta
Bagetta, Giacinto
Corasaniti, Maria Tiziana
Pooled Analysis of Real-World Evidence Supports Anti-CGRP mAbs and OnabotulinumtoxinA Combined Trial in Chronic Migraine
title Pooled Analysis of Real-World Evidence Supports Anti-CGRP mAbs and OnabotulinumtoxinA Combined Trial in Chronic Migraine
title_full Pooled Analysis of Real-World Evidence Supports Anti-CGRP mAbs and OnabotulinumtoxinA Combined Trial in Chronic Migraine
title_fullStr Pooled Analysis of Real-World Evidence Supports Anti-CGRP mAbs and OnabotulinumtoxinA Combined Trial in Chronic Migraine
title_full_unstemmed Pooled Analysis of Real-World Evidence Supports Anti-CGRP mAbs and OnabotulinumtoxinA Combined Trial in Chronic Migraine
title_short Pooled Analysis of Real-World Evidence Supports Anti-CGRP mAbs and OnabotulinumtoxinA Combined Trial in Chronic Migraine
title_sort pooled analysis of real-world evidence supports anti-cgrp mabs and onabotulinumtoxina combined trial in chronic migraine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9413678/
https://www.ncbi.nlm.nih.gov/pubmed/36006191
http://dx.doi.org/10.3390/toxins14080529
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