Evidence map›Paper›PMID 40808545›Full record

ArticleEuropean journal of neurology2025

Effects of Pausing and Re-Initiating Fremanezumab After Continuous 24-Month Treatment for Preventing Difficult-To-Treat Migraine: Prospective, Multicenter, Real-World Data From the GRASP Study Group.

Andreas A Argyriou, Emmanouil V Dermitzakis, Georgia Xiromerisiou, Maria Chondrogianni, Aikaterini Foska, Panagiotis Soldatos, Eleni Mavraki, Dimitrios Rikos, Pantelis Litsardopoulos, Georgios Tsivgoulis and 1 more

Abstract readMulticenter Study
In one paragraph

Article in European journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Andreas A ArgyriouHeadache Outpatient Clinic; Neurology Department, Agios Andreas General Hospital of Patras, Patras, Greece.
Emmanouil V DermitzakisHeadache Clinic, Euromedica General Clinic, Thessaloniki, Greece.
Georgia XiromerisiouDepartment of Neurology, School of Medicine, University of Thessaly, Larissa, Greece.
Maria ChondrogianniSecond Department of Neurology, National and Kapodistrian University of Athens, School of Medicine, 'Attikon' University Hospital, Athens, Greece.
Aikaterini FoskaSecond Department of Neurology, National and Kapodistrian University of Athens, School of Medicine, 'Attikon' University Hospital, Athens, Greece.
Panagiotis SoldatosKalamata, Headache Clinic, Kalamata, Greece.
Eleni MavrakiNeurology Department, Democritus University of Thrace, Alexandroupolis, Greece.
Dimitrios Rikos404 Military Hospital, Larisa, Greece.
Pantelis LitsardopoulosHeadache Outpatient Clinic; Neurology Department, Agios Andreas General Hospital of Patras, Patras, Greece.
Georgios TsivgoulisSecond Department of Neurology, National and Kapodistrian University of Athens, School of Medicine, 'Attikon' University Hospital, Athens, Greece.ORCID 0000-0002-0640-3797
Michail VikelisGlyfada, Headache Clinic, Glyfada, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study, designed by the Greek Research Alliance for Studying headache and Pain (GRASP), aimed to (i) prospectively evaluate the effects of treatment cessation in fremanezumab-responsive patients after 2 years exposure and (ii) assess variations in response rates after migraine worsening and treatment re-initiation.

methodsWe analyzed 149 patients with high-frequency episodic (HFEM) or chronic migraine (CM), who completed 24 months of fremanezumab, and mandatorily paused fremanezumab and re-initiated it after their migraine worsened. To assess longitudinal variations mostly in monthly migraine/headache days (MMD/MHD) and other efficacy variables, patients were interviewed at baseline (T0), at month 3 (T1), month 24 (T2), treatment pause period (T3), and at month 3 after fremanezumab re-initiation (T4). The primary objective was to assess the ≥ 50% and ≥ 75% response rates at T4, compared to T3 and T2.

resultsMigraine relapsed in previous responders at T3, while fremanezumab re-initiation was not equally effective, as evidenced by lower ≥ 50% response rates, mostly in CM. At T4, 6 (9.7%) previously responsive HFEM patients and 27 (31%) previously responsive CM patients failed to obtain ≥ 50% MMD/MHD reduction, compared to T3. The rate of both HFEM and CM super-responders, obtaining a ≥ 75% response at T3, also dropped at T4.

conclusionDiscontinuation of fremanezumab after month 24 leads to rising MMD/MHDs. After fremanezumab re-initiation, a relatively reduced effectiveness in the first 3 months might occur, compared with the pre-fremanezumab cessation. Overall, our findings doubt the rationale behind mandated anti-CGRP treatment pauses in migraine prophylaxis.

Indexed as

Antibodies, MonoclonalMigraine DisordersAdultFemaleHumansMaleMiddle AgedProspective StudiesTreatment OutcomeAntibodies, MonoclonalfremanezumabCGRPfremanezumabmandatory cessationmigraine preventionmonoclonal antibodiesre‐initiation

Identifiers

PMID40808545
PMCPMC12351124

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.