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Lasmiditan for Patients with Migraine and Contraindications to Triptans: A Post Hoc Analysis
INTRODUCTION: As 5-HT(1B) receptor agonists, triptans produce vasoconstriction and have cardiovascular contraindications and precautions. Lasmiditan, a selective 5-HT(1F) receptor agonist, has a low affinity for 5-HT(1B) receptors, does not cause vasoconstriction, and is free of cardiovascular contr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Healthcare
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098729/ https://www.ncbi.nlm.nih.gov/pubmed/35471625 http://dx.doi.org/10.1007/s40122-022-00388-8 |
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author | Krege, John H. Lipton, Richard B. Baygani, Simin K. Komori, Mika Ryan, Sinéad M. Vincent, Maurice |
author_facet | Krege, John H. Lipton, Richard B. Baygani, Simin K. Komori, Mika Ryan, Sinéad M. Vincent, Maurice |
author_sort | Krege, John H. |
collection | PubMed |
description | INTRODUCTION: As 5-HT(1B) receptor agonists, triptans produce vasoconstriction and have cardiovascular contraindications and precautions. Lasmiditan, a selective 5-HT(1F) receptor agonist, has a low affinity for 5-HT(1B) receptors, does not cause vasoconstriction, and is free of cardiovascular contraindications and precautions. The objective of this post hoc analysis was to evaluate the efficacy and safety of lasmiditan in patients with and without at least one triptan contraindication. METHODS: Patient subgroups, with and without triptan contraindications, were analyzed from pooled patient data from four randomized, double-blind, placebo-controlled clinical trials (SAMURAI, SPARTAN, CENTURION, and MONONOFU). Patients experiencing a single migraine attack of moderate or severe intensity were treated with lasmiditan 50 mg (SPARTAN and MONONOFU only), 100 mg, 200 mg, or placebo, and efficacy data were recorded in an electronic diary. RESULTS: Of 5704 patients, 207 (3.6%) patients had at least one contraindication to triptans. Overall subgroup analysis revealed that the effects of lasmiditan on pain freedom, pain relief, freedom from most bothersome symptom, disability freedom, and Patient Global Impression of Change at 2 h post-dose did not differ in patient groups with and without triptan contraindications. These outcomes generally showed a similar benefit pattern for lasmiditan in both subgroups, with all results being statistically significant in patients without contraindications, and pain relief being statistically significant in patients with contraindications. The safety and tolerability profiles of patients with triptan versus without triptan contraindications were similar, including dizziness in 18.3 to 22.8% and somnolence in 7.9 to 9.9% of patients at the highest dose of lasmiditan. CONCLUSIONS: In pooled analyses from four trials, patients with and without triptan contraindications did not differ in their patterns of lasmiditan efficacy. Lasmiditan may be a treatment option in patients with contraindications to triptans. TRIAL REGISTRATION NUMBERS: SAMURAI, NCT:02439320; SPARTAN, NCT:02605174; CENTURION, NCT:03670810; and MONONOFU, NCT:03962738. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40122-022-00388-8. |
format | Online Article Text |
id | pubmed-9098729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-90987292022-05-14 Lasmiditan for Patients with Migraine and Contraindications to Triptans: A Post Hoc Analysis Krege, John H. Lipton, Richard B. Baygani, Simin K. Komori, Mika Ryan, Sinéad M. Vincent, Maurice Pain Ther Original Research INTRODUCTION: As 5-HT(1B) receptor agonists, triptans produce vasoconstriction and have cardiovascular contraindications and precautions. Lasmiditan, a selective 5-HT(1F) receptor agonist, has a low affinity for 5-HT(1B) receptors, does not cause vasoconstriction, and is free of cardiovascular contraindications and precautions. The objective of this post hoc analysis was to evaluate the efficacy and safety of lasmiditan in patients with and without at least one triptan contraindication. METHODS: Patient subgroups, with and without triptan contraindications, were analyzed from pooled patient data from four randomized, double-blind, placebo-controlled clinical trials (SAMURAI, SPARTAN, CENTURION, and MONONOFU). Patients experiencing a single migraine attack of moderate or severe intensity were treated with lasmiditan 50 mg (SPARTAN and MONONOFU only), 100 mg, 200 mg, or placebo, and efficacy data were recorded in an electronic diary. RESULTS: Of 5704 patients, 207 (3.6%) patients had at least one contraindication to triptans. Overall subgroup analysis revealed that the effects of lasmiditan on pain freedom, pain relief, freedom from most bothersome symptom, disability freedom, and Patient Global Impression of Change at 2 h post-dose did not differ in patient groups with and without triptan contraindications. These outcomes generally showed a similar benefit pattern for lasmiditan in both subgroups, with all results being statistically significant in patients without contraindications, and pain relief being statistically significant in patients with contraindications. The safety and tolerability profiles of patients with triptan versus without triptan contraindications were similar, including dizziness in 18.3 to 22.8% and somnolence in 7.9 to 9.9% of patients at the highest dose of lasmiditan. CONCLUSIONS: In pooled analyses from four trials, patients with and without triptan contraindications did not differ in their patterns of lasmiditan efficacy. Lasmiditan may be a treatment option in patients with contraindications to triptans. TRIAL REGISTRATION NUMBERS: SAMURAI, NCT:02439320; SPARTAN, NCT:02605174; CENTURION, NCT:03670810; and MONONOFU, NCT:03962738. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40122-022-00388-8. Springer Healthcare 2022-04-26 2022-06 /pmc/articles/PMC9098729/ /pubmed/35471625 http://dx.doi.org/10.1007/s40122-022-00388-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Original Research Krege, John H. Lipton, Richard B. Baygani, Simin K. Komori, Mika Ryan, Sinéad M. Vincent, Maurice Lasmiditan for Patients with Migraine and Contraindications to Triptans: A Post Hoc Analysis |
title | Lasmiditan for Patients with Migraine and Contraindications to Triptans: A Post Hoc Analysis |
title_full | Lasmiditan for Patients with Migraine and Contraindications to Triptans: A Post Hoc Analysis |
title_fullStr | Lasmiditan for Patients with Migraine and Contraindications to Triptans: A Post Hoc Analysis |
title_full_unstemmed | Lasmiditan for Patients with Migraine and Contraindications to Triptans: A Post Hoc Analysis |
title_short | Lasmiditan for Patients with Migraine and Contraindications to Triptans: A Post Hoc Analysis |
title_sort | lasmiditan for patients with migraine and contraindications to triptans: a post hoc analysis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098729/ https://www.ncbi.nlm.nih.gov/pubmed/35471625 http://dx.doi.org/10.1007/s40122-022-00388-8 |
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