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Predictors of response to erenumab after 12 months of treatment
OBJECTIVE: Erenumab is a monoclonal antibody acting against calcitonin gene‐related peptide receptor and approved for the preventive treatment of chronic migraine. The aim of the present study is to identify clinical predictors of good response in patients with chronic migraine and medication overus...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413721/ https://www.ncbi.nlm.nih.gov/pubmed/34268907 http://dx.doi.org/10.1002/brb3.2260 |
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author | Baraldi, Carlo Castro, Flavia Lo Cainazzo, Maria Michela Pani, Luca Guerzoni, Simona |
author_facet | Baraldi, Carlo Castro, Flavia Lo Cainazzo, Maria Michela Pani, Luca Guerzoni, Simona |
author_sort | Baraldi, Carlo |
collection | PubMed |
description | OBJECTIVE: Erenumab is a monoclonal antibody acting against calcitonin gene‐related peptide receptor and approved for the preventive treatment of chronic migraine. The aim of the present study is to identify clinical predictors of good response in patients with chronic migraine and medication overuse‐headache. MATERIAL AND METHODS: This was a retrospective single‐center not funded study. Enrolled patients were affected by chronic migraine and medication overuse‐headache treated with erenumab monthly, up to 1 year. At 1 year, patients were classified as good responders if they displayed a ≥50% reduction in the number of headache days per months compared to the baseline. RESULTS: After 1 year, a significant improvement in the number of headache days per months, analgesic consumption, 6‐items headache impact test, and migraine disability assessment questionnaire scores were obtained compared to the baseline. Patients who obtained a ≥50% reduction in the number of headache days per month compared to the baseline displayed a longer history of medication overuse‐headache, a higher number of painkillers taken per month at the baseline and a higher number of failed preventive treatments in the past. CONCLUSIONS: Patients with longer medication overuse‐headache duration, higher analgesic intake, and a higher number of previous preventive treatment failures may receive less benefit with erenumab. |
format | Online Article Text |
id | pubmed-8413721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84137212021-09-07 Predictors of response to erenumab after 12 months of treatment Baraldi, Carlo Castro, Flavia Lo Cainazzo, Maria Michela Pani, Luca Guerzoni, Simona Brain Behav Original Research OBJECTIVE: Erenumab is a monoclonal antibody acting against calcitonin gene‐related peptide receptor and approved for the preventive treatment of chronic migraine. The aim of the present study is to identify clinical predictors of good response in patients with chronic migraine and medication overuse‐headache. MATERIAL AND METHODS: This was a retrospective single‐center not funded study. Enrolled patients were affected by chronic migraine and medication overuse‐headache treated with erenumab monthly, up to 1 year. At 1 year, patients were classified as good responders if they displayed a ≥50% reduction in the number of headache days per months compared to the baseline. RESULTS: After 1 year, a significant improvement in the number of headache days per months, analgesic consumption, 6‐items headache impact test, and migraine disability assessment questionnaire scores were obtained compared to the baseline. Patients who obtained a ≥50% reduction in the number of headache days per month compared to the baseline displayed a longer history of medication overuse‐headache, a higher number of painkillers taken per month at the baseline and a higher number of failed preventive treatments in the past. CONCLUSIONS: Patients with longer medication overuse‐headache duration, higher analgesic intake, and a higher number of previous preventive treatment failures may receive less benefit with erenumab. John Wiley and Sons Inc. 2021-07-16 /pmc/articles/PMC8413721/ /pubmed/34268907 http://dx.doi.org/10.1002/brb3.2260 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Baraldi, Carlo Castro, Flavia Lo Cainazzo, Maria Michela Pani, Luca Guerzoni, Simona Predictors of response to erenumab after 12 months of treatment |
title | Predictors of response to erenumab after 12 months of treatment |
title_full | Predictors of response to erenumab after 12 months of treatment |
title_fullStr | Predictors of response to erenumab after 12 months of treatment |
title_full_unstemmed | Predictors of response to erenumab after 12 months of treatment |
title_short | Predictors of response to erenumab after 12 months of treatment |
title_sort | predictors of response to erenumab after 12 months of treatment |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413721/ https://www.ncbi.nlm.nih.gov/pubmed/34268907 http://dx.doi.org/10.1002/brb3.2260 |
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