Effectiveness and safety of monthly versus quarterly fremanezumab for migraine prevention: An Italian, multicenter, real‐life study

Author:

Zanandrea Laura123,Messina Roberta123ORCID,Cetta Ilaria123,Genovese Federica123,Guerrieri Simone1,Vernieri Fabrizio45ORCID,Altamura Claudia45,Cevoli Sabina6,Favoni Valentina6ORCID,Colombo Bruno1,Filippi Massimo123ORCID

Affiliation:

1. Neurology Unit IRCCS San Raffaele Scientific Institute Milan Italy

2. Neuroimaging Research Unit, Division of Neuroscience IRCCS San Raffaele Scientific Institute Milan Italy

3. Vita‐Salute San Raffaele University Milan Italy

4. Unit of Headache and Neurosonology, Department of Medicine and Surgery University Campus Bio‐Medico di Roma Rome Italy

5. Fondazione Policlinico Universitario Campus Bio‐Medico Rome Italy

6. IRCCS Istituto delle Scienze Neurologiche di Bologna Bologna Italy

Abstract

AbstractBackground and PurposeFremanezumab, a monoclonal antibody targeting the calcitonin gene‐related peptide for migraine prevention, is available in monthly (225 mg) and quarterly (675 mg) doses. Previous studies showed efficacy and safety for both regimens, but a real‐life comparison is lacking. This study aimed to compare the effectiveness and safety of monthly and quarterly fremanezumab in a real‐life setting.MethodsThis Italian, prospective, multicenter study enrolled 95 migraine patients. During a 3‐month treatment period, patients received either monthly or quarterly fremanezumab (49 monthly, 46 quarterly). A 6‐month treatment period involved 79 patients (43 monthly, 36 quarterly). Monthly headache (MHD) and migraine days (MMD), number of days (AMD) and pills (AMP) of acute medication intake, and Headache Impact Test (HIT‐6), Migraine Disability Assessment (MIDAS) test, and Numeric Rating Scale (NRS) scores were recorded at baseline and after 3 and 6 months of treatment. Adverse events (AEs), responder rates, and medication overuse were also investigated.ResultsBoth monthly and quarterly treatments led to significant reductions in MMD, MHD, AMP, AMD, HIT‐6, MIDAS, and NRS scores after 3 and 6 months. The monthly regimen exhibited a slightly greater reduction in MMD and MHD after the first quarter, with no significant difference observed after 6 months. The most common AE was transient injection‐site reaction, without between‐group differences. Responder rates and resolution of medication overuse did not significantly differ between the groups.ConclusionsBoth monthly and quarterly regimens were effective and safe, with a tendency for an advantage of the monthly regimen only in the first quarter of treatment.

Publisher

Wiley

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