Evidence map›Paper›PMID 39111884›Full record

Observational studyInternal medicine (Tokyo, Japan)2025

Real-world Efficacy of Erenumab on Migraine-associated Symptoms and Patient-reported Satisfaction Levels: A Retrospective Study in Japan.

Keiko Ihara, Nobuyuki Takahashi, Seiya Ohtani, Narumi Watanabe, Kei Ishizuchi, Ryo Takemura, Daiki Tokuyasu, Koji Sekiguchi, Naoki Miyazaki, Shungo Imai and 3 more

Abstract readObservational Study
In one paragraph

Observational study in Internal medicine (Tokyo, Japan), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Observational
  6. Article
  7. Article
  8. 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

13 authors.

Keiko IharaDepartment of Neurology, Keio University School of Medicine, Japan.
Nobuyuki TakahashiDepartment of Neurology, Keio University School of Medicine, Japan.
Seiya OhtaniDepartment of Neurology, Keio University School of Medicine, Japan.
Narumi WatanabeDepartment of Neurology, Keio University School of Medicine, Japan.
Kei IshizuchiDepartment of Neurology, Keio University School of Medicine, Japan.
Ryo TakemuraBiostatistics Unit, Clinical and Translational Research Center, Keio University Hospital, Japan.
Daiki TokuyasuDepartment of Neurology, Keio University School of Medicine, Japan.
Koji SekiguchiDepartment of Neurology, Keio University School of Medicine, Japan.
Naoki MiyazakiBiostatistics Unit, Clinical and Translational Research Center, Keio University Hospital, Japan.
Shungo ImaiDivision of Drug Informatics, Keio University Faculty of Pharmacy, Japan.
Satoko HoriDivision of Drug Informatics, Keio University Faculty of Pharmacy, Japan.
Jin NakaharaDepartment of Neurology, Keio University School of Medicine, Japan.
Tsubasa TakizawaDepartment of Neurology, Keio University School of Medicine, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective In randomized clinical trials and real-world studies, calcitonin gene-related peptide (CGRP) monoclonal antibodies (mAbs), including erenumab, have demonstrated efficacy for migraine prevention. However, there have been no real-world studies focusing on erenumab in East Asia that investigated its efficacy on migraine-associated symptoms and patient-reported satisfaction levels. Methods This single-center, observational, retrospective, real-world study examined patients who received at least three doses of erenumab at Keio University Hospital, Tokyo, Japan, between December 2021 and March 2023 as their first CGRP mAb treatment in a real-world setting. The patients were administered 70 mg of erenumab monthly. We assessed changes in monthly migraine days (MMDs), responder rates, migraine-associated symptoms including photophobia, phonophobia, nausea/vomiting, and patient-reported satisfaction levels. In addition, injection site reactions and other adverse events were recorded to investigate safety. Results Nineteen patients were considered eligible for the analysis. At 3 months, erenumab decreased MMDs by 6.6 (95% confidence interval, 2.3-10.8; p<0.01). The 50% responder rate was 42%. A total of 83% (n=15), 56% (n=10), and 71% (n=10) of patients reported either improvement in or disappearance of photophobia, phonophobia, and nausea/vomiting, respectively, and 44% (n=8) and 28% (n=5) answered "very satisfied" and "somewhat satisfied", respectively, with erenumab treatment, leaving only 28% (n=5) as "unsatisfied". Injection site reactions (n=6, 32%) and constipation (n=4, 21%) were frequent adverse events. Conclusion In a real-world setting in Japan, erenumab proved to be effective in not only reducing migraine and headache frequency but also improving migraine-associated symptoms and satisfying the majority of patients.

Indexed as

Antibodies, Monoclonal, HumanizedCalcitonin Gene-Related Peptide Receptor AntagonistsMigraine DisordersPatient SatisfactionAdultAgedFemaleHumansJapanMaleMiddle AgedPatient Reported Outcome MeasuresRetrospective StudiesTreatment OutcomeAntibodies, Monoclonal, HumanizedCalcitonin Gene-Related Peptide Receptor Antagonistserenumaberenumabmigrainemigraine-associated symptomsreal-world evidencesatisfaction

Identifiers

PMID39111884
PMCPMC11986316

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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.