Home > Publications Database > Pooled Analysis of Real-World Evidence Supports Anti-CGRP mAbs and OnabotulinumtoxinA Combined Trial in Chronic Migraine. > print |
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024 | 7 | _ | |a 10.3390/toxins14080529 |2 doi |
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037 | _ | _ | |a DZNE-2022-01439 |
041 | _ | _ | |a English |
082 | _ | _ | |a 610 |
100 | 1 | _ | |a Scuteri, Damiana |0 0000-0001-5846-7058 |b 0 |
245 | _ | _ | |a Pooled Analysis of Real-World Evidence Supports Anti-CGRP mAbs and OnabotulinumtoxinA Combined Trial in Chronic Migraine. |
260 | _ | _ | |a Basel |c 2022 |b MDPI |
336 | 7 | _ | |a article |2 DRIVER |
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336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1664543465_12115 |2 PUB:(DE-HGF) |
336 | 7 | _ | |a ARTICLE |2 BibTeX |
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336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
500 | _ | _ | |a CC BY: https://creativecommons.org/licenses/by/4.0/ |
520 | _ | _ | |a 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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650 | _ | 7 | |a PRISMA 2020 |2 Other |
650 | _ | 7 | |a anti-CGRP monoclonal antibodies |2 Other |
650 | _ | 7 | |a migraine |2 Other |
650 | _ | 7 | |a onabotulinumtoxinA |2 Other |
650 | _ | 7 | |a pooled analysis |2 Other |
650 | _ | 7 | |a Antibodies, Monoclonal |2 NLM Chemicals |
650 | _ | 7 | |a Botulinum Toxins, Type A |0 EC 3.4.24.69 |2 NLM Chemicals |
650 | _ | 7 | |a Calcitonin Gene-Related Peptide |0 JHB2QIZ69Z |2 NLM Chemicals |
650 | _ | 2 | |a Antibodies, Monoclonal: therapeutic use |2 MeSH |
650 | _ | 2 | |a Botulinum Toxins, Type A: therapeutic use |2 MeSH |
650 | _ | 2 | |a Calcitonin Gene-Related Peptide: antagonists & inhibitors |2 MeSH |
650 | _ | 2 | |a Drug Therapy, Combination: adverse effects |2 MeSH |
650 | _ | 2 | |a Humans |2 MeSH |
650 | _ | 2 | |a Migraine Disorders: prevention & control |2 MeSH |
650 | _ | 2 | |a Treatment Outcome |2 MeSH |
700 | 1 | _ | |a Tonin, Paolo |0 0000-0002-4867-1378 |b 1 |
700 | 1 | _ | |a Nicotera, Pierluigi |0 P:(DE-2719)2010732 |b 2 |u dzne |
700 | 1 | _ | |a Vulnera, Marilù |b 3 |
700 | 1 | _ | |a Altieri, Giuseppina Cristina |b 4 |
700 | 1 | _ | |a Tarsitano, Assunta |b 5 |
700 | 1 | _ | |a Bagetta, Giacinto |0 0000-0001-8540-6218 |b 6 |
700 | 1 | _ | |a Corasaniti, Maria Tiziana |0 0000-0001-6472-0697 |b 7 |
770 | _ | _ | |a Botulinum Neurotoxin: Shared/Common Mechanisms in the Treatment of Pain, Spasticity and Movement Disorders |
773 | _ | _ | |a 10.3390/toxins14080529 |g Vol. 14, no. 8, p. 529 - |0 PERI:(DE-600)2518395-3 |n 8 |p 529 |t Toxins |v 14 |y 2022 |x 2072-6651 |
856 | 4 | _ | |y OpenAccess |u https://pub.dzne.de/record/165134/files/DZNE-2022-01439.pdf |
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