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One-Time Use of Galcanezumab or Fremanezumab for Migraine Prevention

Background There are no reports on the effectiveness of one-time use of the calcitonin gene-related peptide-related monoclonal antibodies (CGRP-mABs) evaluated at one and three months for migraine prevention. Here, we present the real-world data of one-time administration of CGRP-mABs, galcanezumab...

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Autores principales: Katsuki, Masahito, Kashiwagi, Kenta, Kawamura, Shin, Tachikawa, Senju, Koh, Akihito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951121/
https://www.ncbi.nlm.nih.gov/pubmed/36843788
http://dx.doi.org/10.7759/cureus.34180
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author Katsuki, Masahito
Kashiwagi, Kenta
Kawamura, Shin
Tachikawa, Senju
Koh, Akihito
author_facet Katsuki, Masahito
Kashiwagi, Kenta
Kawamura, Shin
Tachikawa, Senju
Koh, Akihito
author_sort Katsuki, Masahito
collection PubMed
description Background There are no reports on the effectiveness of one-time use of the calcitonin gene-related peptide-related monoclonal antibodies (CGRP-mABs) evaluated at one and three months for migraine prevention. Here, we present the real-world data of one-time administration of CGRP-mABs, galcanezumab and fremanezumab, for migraine prevention. Methodology We retrospectively investigated eight migraine patients treated with one-time administration of galcanezumab 240 mg or fremanezumab 225 mg. Monthly headache days (MHD), monthly acute medication intake days (AMD), and Headache Impact Test-6 (HIT-6) scores before, one, and three months after one-time CGRP-mABs administration were evaluated. Results A total of five women and three men were included (median age = 46.5 years, range = 19-63 years). Overall, six were episodic migraine, and two were chronic migraine. Five patients received one-time administration of fremanezumab and three received galcanezumab. In total, six (75.0%) patients experienced therapeutic effectiveness one month after the one-time administration. Five of the six maintained the therapeutic effect until three months, but one had aggravation. As a result, six (75.0%) patients reached or maintained therapeutic conditions three months after the one-time administration of CGRP-mABs without side effects. All patients continued previously used oral prophylaxis during the observational period. Significant reductions in MHD, AMD, and HIT-6 scores were observed three months after the initial administration (p = 0.008, p = 0.005, and p < 0.001, respectively). Conclusions Six of the eight patients experienced or maintained therapeutic effectiveness at three months despite the one-time administration of CGRP-mABs. Our results suggest that one-time use of CGRP-mABs may be a new treatment option in combination with oral prophylaxis.
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spelling pubmed-99511212023-02-25 One-Time Use of Galcanezumab or Fremanezumab for Migraine Prevention Katsuki, Masahito Kashiwagi, Kenta Kawamura, Shin Tachikawa, Senju Koh, Akihito Cureus Internal Medicine Background There are no reports on the effectiveness of one-time use of the calcitonin gene-related peptide-related monoclonal antibodies (CGRP-mABs) evaluated at one and three months for migraine prevention. Here, we present the real-world data of one-time administration of CGRP-mABs, galcanezumab and fremanezumab, for migraine prevention. Methodology We retrospectively investigated eight migraine patients treated with one-time administration of galcanezumab 240 mg or fremanezumab 225 mg. Monthly headache days (MHD), monthly acute medication intake days (AMD), and Headache Impact Test-6 (HIT-6) scores before, one, and three months after one-time CGRP-mABs administration were evaluated. Results A total of five women and three men were included (median age = 46.5 years, range = 19-63 years). Overall, six were episodic migraine, and two were chronic migraine. Five patients received one-time administration of fremanezumab and three received galcanezumab. In total, six (75.0%) patients experienced therapeutic effectiveness one month after the one-time administration. Five of the six maintained the therapeutic effect until three months, but one had aggravation. As a result, six (75.0%) patients reached or maintained therapeutic conditions three months after the one-time administration of CGRP-mABs without side effects. All patients continued previously used oral prophylaxis during the observational period. Significant reductions in MHD, AMD, and HIT-6 scores were observed three months after the initial administration (p = 0.008, p = 0.005, and p < 0.001, respectively). Conclusions Six of the eight patients experienced or maintained therapeutic effectiveness at three months despite the one-time administration of CGRP-mABs. Our results suggest that one-time use of CGRP-mABs may be a new treatment option in combination with oral prophylaxis. Cureus 2023-01-25 /pmc/articles/PMC9951121/ /pubmed/36843788 http://dx.doi.org/10.7759/cureus.34180 Text en Copyright © 2023, Katsuki et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Katsuki, Masahito
Kashiwagi, Kenta
Kawamura, Shin
Tachikawa, Senju
Koh, Akihito
One-Time Use of Galcanezumab or Fremanezumab for Migraine Prevention
title One-Time Use of Galcanezumab or Fremanezumab for Migraine Prevention
title_full One-Time Use of Galcanezumab or Fremanezumab for Migraine Prevention
title_fullStr One-Time Use of Galcanezumab or Fremanezumab for Migraine Prevention
title_full_unstemmed One-Time Use of Galcanezumab or Fremanezumab for Migraine Prevention
title_short One-Time Use of Galcanezumab or Fremanezumab for Migraine Prevention
title_sort one-time use of galcanezumab or fremanezumab for migraine prevention
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951121/
https://www.ncbi.nlm.nih.gov/pubmed/36843788
http://dx.doi.org/10.7759/cureus.34180
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