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Likelihood of response with subsequent dosing for patients with migraine and initial suboptimal response with eptinezumab: A post hoc analysis of two placebo‐controlled randomized clinical trials
OBJECTIVE: To develop a multivariable model assessing factors predicting a second‐dose response to eptinezumab treatment over weeks 13–24 in patients with migraine initially reporting a suboptimal response over weeks 1–12. BACKGROUND: Eptinezumab is a monoclonal antibody used for migraine prevention...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321567/ https://www.ncbi.nlm.nih.gov/pubmed/35524405 http://dx.doi.org/10.1111/head.14302 |
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author | Schim, Jack D. Anderson, Carlton Brunner, Elizabeth Hirman, Joe Ogbru, Annette Cady, Roger McGill, Lora |
author_facet | Schim, Jack D. Anderson, Carlton Brunner, Elizabeth Hirman, Joe Ogbru, Annette Cady, Roger McGill, Lora |
author_sort | Schim, Jack D. |
collection | PubMed |
description | OBJECTIVE: To develop a multivariable model assessing factors predicting a second‐dose response to eptinezumab treatment over weeks 13–24 in patients with migraine initially reporting a suboptimal response over weeks 1–12. BACKGROUND: Eptinezumab is a monoclonal antibody used for migraine prevention, administered every 12 weeks. In the PROMISE‐1 and PROMISE‐2 studies, the first‐dose response to eptinezumab treatment (≥50% monthly migraine day [MMD] reduction over weeks 1–12) occurred in ~50–60% of patients with episodic (EM) and chronic migraine (CM), respectively. METHODS: This post hoc analysis included patients with suboptimal first‐dose response (<50% MMD reduction over weeks 1–12) with EM and CM, with patient‐reported outcome data at weeks 12 and 24. Eptinezumab 100 and 300 mg doses were pooled. RESULTS: The analysis included 416/888 patients (46.8%) from PROMISE‐1 and 479/1072 patients (44.7%) from PROMISE‐2 with suboptimal first‐dose response. The proportion of suboptimal first‐dose responders who were second‐dose responders was 37.0% (71/192; eptinezumab) and 33.9% (42/124; placebo) in PROMISE‐1 and 28.8% (79/274) and 18.5% (38/205) in PROMISE‐2. Significant first‐dose predictors of second‐dose response were percent change in MMDs across weeks 1–12 (PROMISE‐1, odds ratio [OR]: 0.97, 95% confidence interval [CI]: 0.95, 0.98, p = 0.0001; PROMISE‐2, OR: 0.94, CI: 0.92, 0.96, p < 0.0001) and change in 6‐item Headache Impact Test (HIT‐6) total score (PROMISE‐2 only, OR: 0.92; CI: 0.87, 0.98; p = 0.027). In PROMISE‐1, the probability of second‐dose response ranged from 21.7% in patients with first‐dose 0% MMD change to 56.0% in patients with first‐dose 45% MMD reduction. In PROMISE‐2, depending on HIT‐6 total score, probability of second‐dose response ranged from 5.9–12.1% in patients with first‐dose 0% MMD change to 54.2%–72.3% in patients with first‐dose 45.0% MMD reduction. CONCLUSION: Individuals with migraine not experiencing ≥50% MMD response to their first dose of eptinezumab may benefit from a second dose. |
format | Online Article Text |
id | pubmed-9321567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93215672022-07-30 Likelihood of response with subsequent dosing for patients with migraine and initial suboptimal response with eptinezumab: A post hoc analysis of two placebo‐controlled randomized clinical trials Schim, Jack D. Anderson, Carlton Brunner, Elizabeth Hirman, Joe Ogbru, Annette Cady, Roger McGill, Lora Headache Research Submissions OBJECTIVE: To develop a multivariable model assessing factors predicting a second‐dose response to eptinezumab treatment over weeks 13–24 in patients with migraine initially reporting a suboptimal response over weeks 1–12. BACKGROUND: Eptinezumab is a monoclonal antibody used for migraine prevention, administered every 12 weeks. In the PROMISE‐1 and PROMISE‐2 studies, the first‐dose response to eptinezumab treatment (≥50% monthly migraine day [MMD] reduction over weeks 1–12) occurred in ~50–60% of patients with episodic (EM) and chronic migraine (CM), respectively. METHODS: This post hoc analysis included patients with suboptimal first‐dose response (<50% MMD reduction over weeks 1–12) with EM and CM, with patient‐reported outcome data at weeks 12 and 24. Eptinezumab 100 and 300 mg doses were pooled. RESULTS: The analysis included 416/888 patients (46.8%) from PROMISE‐1 and 479/1072 patients (44.7%) from PROMISE‐2 with suboptimal first‐dose response. The proportion of suboptimal first‐dose responders who were second‐dose responders was 37.0% (71/192; eptinezumab) and 33.9% (42/124; placebo) in PROMISE‐1 and 28.8% (79/274) and 18.5% (38/205) in PROMISE‐2. Significant first‐dose predictors of second‐dose response were percent change in MMDs across weeks 1–12 (PROMISE‐1, odds ratio [OR]: 0.97, 95% confidence interval [CI]: 0.95, 0.98, p = 0.0001; PROMISE‐2, OR: 0.94, CI: 0.92, 0.96, p < 0.0001) and change in 6‐item Headache Impact Test (HIT‐6) total score (PROMISE‐2 only, OR: 0.92; CI: 0.87, 0.98; p = 0.027). In PROMISE‐1, the probability of second‐dose response ranged from 21.7% in patients with first‐dose 0% MMD change to 56.0% in patients with first‐dose 45% MMD reduction. In PROMISE‐2, depending on HIT‐6 total score, probability of second‐dose response ranged from 5.9–12.1% in patients with first‐dose 0% MMD change to 54.2%–72.3% in patients with first‐dose 45.0% MMD reduction. CONCLUSION: Individuals with migraine not experiencing ≥50% MMD response to their first dose of eptinezumab may benefit from a second dose. John Wiley and Sons Inc. 2022-05-06 2022-05 /pmc/articles/PMC9321567/ /pubmed/35524405 http://dx.doi.org/10.1111/head.14302 Text en © 2022 The Authors. Headache: The Journal of Head and Face Pain published by Wiley Periodicals LLC on behalf of American Headache Society https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Submissions Schim, Jack D. Anderson, Carlton Brunner, Elizabeth Hirman, Joe Ogbru, Annette Cady, Roger McGill, Lora Likelihood of response with subsequent dosing for patients with migraine and initial suboptimal response with eptinezumab: A post hoc analysis of two placebo‐controlled randomized clinical trials |
title | Likelihood of response with subsequent dosing for patients with migraine and initial suboptimal response with eptinezumab: A post hoc analysis of two placebo‐controlled randomized clinical trials |
title_full | Likelihood of response with subsequent dosing for patients with migraine and initial suboptimal response with eptinezumab: A post hoc analysis of two placebo‐controlled randomized clinical trials |
title_fullStr | Likelihood of response with subsequent dosing for patients with migraine and initial suboptimal response with eptinezumab: A post hoc analysis of two placebo‐controlled randomized clinical trials |
title_full_unstemmed | Likelihood of response with subsequent dosing for patients with migraine and initial suboptimal response with eptinezumab: A post hoc analysis of two placebo‐controlled randomized clinical trials |
title_short | Likelihood of response with subsequent dosing for patients with migraine and initial suboptimal response with eptinezumab: A post hoc analysis of two placebo‐controlled randomized clinical trials |
title_sort | likelihood of response with subsequent dosing for patients with migraine and initial suboptimal response with eptinezumab: a post hoc analysis of two placebo‐controlled randomized clinical trials |
topic | Research Submissions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321567/ https://www.ncbi.nlm.nih.gov/pubmed/35524405 http://dx.doi.org/10.1111/head.14302 |
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