4.4 Article

Effectiveness and Safety of CGRP-mAbs in Menstrual-Related Migraine: A Real-World Experience

Journal

PAIN AND THERAPY
Volume 10, Issue 2, Pages 1203-1214

Publisher

SPRINGER INT PUBL AG
DOI: 10.1007/s40122-021-00273-w

Keywords

Calcitonin gene-related peptide monoclonal antibody; Menstrual migraine; Migraine; Menstrual-related migraine

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The study showed that CGRP-mAbs could effectively reduce the frequency, intensity, and duration of menstrual migraine attacks in MRM patients who had previous treatment failures, as well as significantly improve the responsiveness to painkillers, indicating the potential of CGRP-mAbs as a safe and effective preventive treatment for menstrual migraines.
Introduction Migraine shows a significantly higher prevalence in women, especially during reproductive age when menstrual-related hormonal fluctuations represent the most common migraine trigger. Indeed, over 50% of patients report a higher occurrence of migraine attacks during the perimenstrual window. Menstrual migraine attacks are consistently referred to as more disabling, less responsive to symptomatic treatments, longer in duration, and more prone to relapse than non-menstrual migraine attacks. Evidence strongly suggests that estrogen fluctuations are involved in migraine attacks worsening during the perimenstrual window through several mechanisms directly or indirectly involving the CGRP pathway. We aimed to evaluate whether mAbs blocking CGRP-ligand or receptor (CGRP-mAbs) could represent an effective and safe preventive treatment for menstrual migraine attacks in patients with menstrual-related migraine (MRM) with previous treatment failures. Methods Forty patients with MRM with at least three previous treatment failures received monthly CGRP-mAbs. At the baseline and after six CGRP-mAbs administrations, patients underwent to extensive interviews to assess frequency, duration, intensity, and responsiveness to painkiller intake of migraine attacks occurring during the perimenstrual window. Results After six administrations of CGRP-mAbs we observed a reduction of median menstrual migraine frequency (from 5 to 2 days per month), pain intensity (from 8/10 to 6/10), and attacks duration (from 24 to 8 h) (p < 0.001). Nevertheless, a significant increase in the percentage of responding to migraine painkillers was observed from 42.5% at baseline to 95% at T1 (p < 0.001). Conclusions CGRP-mAbs could represent a safe and effective preventive therapeutic strategy able to reduce the disabling burden of menstrual migraine attack frequency, duration, intensity, and significantly improve the response to painkillers. These findings could be related to and further indirectly prove the greater influence of CGRP-mediated mechanisms in the pathophysiology of menstrual migraine attacks.

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