Evidence map›Paper›PMID 39066884›Full record

ArticleActa neurologica Belgica2024

Erenumab escalation in migraine - double dose without additional benefit - a retrospective experience.

Simon Heintz, Peter Storch, Philipp Burow, Patricia Maier, Mark Obermann, Grit Stoessel, Torsten Kraya, Steffen Naegel

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Article in Acta neurologica Belgica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Simon HeintzDepartment of Neurology, University Hospital Halle, Martin Luther University Halle- Wittenberg, Wittenberg, Germany.
Peter StorchHeadache Center Jena, Department of Neurology, University Hospital Jena, Jena, Germany.
Philipp BurowDepartment of Neurology, University Hospital Halle, Martin Luther University Halle- Wittenberg, Wittenberg, Germany.
Patricia MaierDepartment of Neurology, University Hospital Halle, Martin Luther University Halle- Wittenberg, Wittenberg, Germany.
Mark ObermannDepartment of Neurology, Klinikum Weser-Egge, Höxter, Germany.
Grit StoesselHeadache Center Jena, Department of Neurology, University Hospital Jena, Jena, Germany.
Torsten KrayaDepartment of Neurology, University Hospital Halle, Martin Luther University Halle- Wittenberg, Wittenberg, Germany.
Steffen NaegelDepartment of Neurology, University Hospital Halle, Martin Luther University Halle- Wittenberg, Wittenberg, Germany. steffen.naegel@medizin.uni-halle.de.ORCID http://orcid.org/0000-0003-1727-9362

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundErenumab is a monoclonal antibody specifically targeting the CGRP-receptor. Several studies showed efficacy and safety in patients with migraine. Less is known regarding dosage increase, especially in a difficult to treat patients. The aim of the study is to evaluate the increased dosage under real world conditions with particular focus on 70 mg non-responders.

methodsIn a retrospective analysis, patients treated in tertiary headache centers (Halle or Jena, Germany) receiving 70 mg erenumab for at least 3 months with a dosage increase to 140 mg were analyzed. Data were evaluated regarding headache days, intake of acute medication, previous prophylaxis, and medication overuse. Baseline and all treatment intervals were determined as three-month periods.

resultsDatasets of 52 migraine patients (90.4% women) aged between 22 and 78 years (mean 50.4 years, SD 12.1 years) were analyzed. At baseline (mean headache-days 15.67 ± 6.37) 51.9% met criteria for chronic migraine and 56% were currently overusing acute medication. While therapy with 70 mg showed significant improvement in headache days and 50% response, further improvement was not achieved for therapy escalation to 140 mg. The same applies to the secondary endpoints and covers the entire study population as well as the subgroups of chronic and episodic migraine. The 50% response of the 70 mg non-responders for escalation was only 5.14%.

conclusionsIn this difficult-to-treat patient cohort we reconfirmed the effectiveness of erenumab, but could not detect any additional benefit for a dosage escalation from 70 mg to 140 mg erenumab.

Indexed as

Antibodies, Monoclonal, HumanizedCalcitonin Gene-Related Peptide Receptor AntagonistsMigraine DisordersAdultAgedDose-Response Relationship, DrugFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeYoung AdultAntibodies, Monoclonal, HumanizedCalcitonin Gene-Related Peptide Receptor AntagonistserenumabErenumabMigrainePreventive medicationReal-world

Identifiers

PMID39066884
PMCPMC11615020

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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.