Effects of Fremanezumab on Psychiatric Comorbidities in Difficult-to-Treat Patients with Chronic Migraine: Post Hoc Analysis of a Prospective, Multicenter, Real-World Greek Registry

Author:

Vikelis Michail1ORCID,Dermitzakis Emmanouil V.2ORCID,Xiromerisiou Georgia3ORCID,Rallis Dimitrios4,Soldatos Panagiotis5,Litsardopoulos Pantelis6,Rikos Dimitrios7ORCID,Argyriou Andreas A.6ORCID

Affiliation:

1. Headache Clinic, Mediterraneo Hospital, 16675 Athens, Greece

2. Euromedica General Clinic, 54645 Thessaloniki, Greece

3. Department of Neurology, University Hospital of Larissa, University of Thessaly, 41110 Larissa, Greece

4. Department of Neurology, Tzaneio General Hospital of Piraeus, 18536 Athens, Greece

5. Independent Researcher, 24100 Kalamata, Greece

6. Headache Outpatient Clinic, Department of Neurology, Agios Andreas State General Hospital of Patras, 26335 Patras, Greece

7. 404 Military Hospital, 41222 Larisa, Greece

Abstract

Objective: this post hoc analysis aimed to evaluate the efficacy of fremanezumab in difficult-to-treat chronic migraine (CM) patients with and without psychiatric comorbidities (PCs), mainly anxiety and/or depression. Methods: We assessed data from CM patients with and without PCs who failed at least 3 preventives and eventually received at least 3 consecutive monthly doses of fremanezumab 225 mg. Outcomes included the crude response (≥50% reduction in monthly headache days (MHDs)) rates to fremanezumab from the baseline to the last clinical follow-up. The changes in MHDs; MHDs of moderate/greater severity; monthly days with intake of abortive medication; and the proportion of patients’ changing status from with PCs to decreased/without PCs were also compared. Disability and quality of life (QOL) outcomes were also assessed. Results: Of 107 patients enrolled, 65 (60.7%) had baseline PCs. The percentage of patients with (n = 38/65; 58.5%) and without (n = 28/42; 66.6%) PCs that achieved a ≥50% reduction in MHDs with fremanezumab was comparable (p = 0.41), whereas MHDs were significantly reduced (difference vs. baseline) in both patients with PCs (mean −8.9 (standard error: 6.8); p < 0.001) and without PCs (−9.8 (7.5); p < 0.001). Both groups experienced significant improvements in all other efficacy, disability, and QOL outcomes at comparable rates, including in MHD reduction. A significant proportion of fremanezumab-treated patients with baseline PCs de-escalated in corresponding severities or even reverted to no PCs (28/65; 43.1%) post-fremanezumab. Conclusions: fremanezumab appears to be effective as a preventive treatment in difficult-to-treat CM patients with and without PCs while also being beneficial in reducing the severity of comorbid anxiety and/or depression.

Funder

Allergan-Abbvie

Elli-Lilly

Novartis

Teva

Lundbeck

Pfizer

Tikun

UCB

ITF Hellas

Innovis

Publisher

MDPI AG

Subject

General Medicine

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