Evidence map›Paper›PMID 39377745›Full record

ArticleAllergy2025

Omalizumab is effective and safe in chronic inducible urticaria (CIndU): Real-world data from a large multi-national UCARE study.

R Soegiharto, M Alizadeh Aghdam, J A Sørensen, E van Lindonk, F Bulut Demir, N Mohammad Porras, Y Matsuo, L Kiefer, A C Knulst, M Maurer and 17 more

Abstract readMulticenter Study
In one paragraph

Article in Allergy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
–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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Guideline
  2. Pooled it
  3. Dupilumab in patients with cold urticaria: Results from a phase 3 trial.The journal of allergy and clinical immunology. Global · 2026
    Article
  4. Article
  5. Exploring the Disease Duration of Urticaria and Associated Determinants in Primary Care.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2026
    Article
  6. Review
  7. Towards Personalised Therapy in Chronic Spontaneous Urticaria: Advancing From Endotype to Clinical Response.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2025
    Review
  8. Review
  9. Article
  10. 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

27 authors.

R SoegihartoDepartment of Dermatology/Allergology, University Medical Centre Utrecht, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-1942-2508
M Alizadeh AghdamDepartment of Dermatology/Allergology, University Medical Centre Utrecht, Utrecht, Netherlands.ORCID https://orcid.org/0000-0003-3584-9250
J A SørensenDepartment of Dermato-Venereology and Wound Healing Centre, University of Copenhagen, Bispebjerg Hospital, Copenhagen, Denmark.
E van LindonkDepartment of Dermatology, Erasmus MC, Rotterdam, Netherlands.
F Bulut DemirDepartment of Dermatology, Marmara University School of Medicine, İstanbul, Turkey.
N Mohammad PorrasDepartment of Dermatology, Hospital del Mar Research Institute. Universitat Pompeu Fabra de Barcelona, Barcelona, Spain.
Y MatsuoDepartment of Dermatology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
L KieferUrticaria Center of Reference and Excellence (UCARE), Institute of Allergology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
A C KnulstDepartment of Dermatology/Allergology, University Medical Centre Utrecht, Utrecht, Netherlands.
M MaurerUrticaria Center of Reference and Excellence (UCARE), Institute of Allergology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.ORCID https://orcid.org/0000-0002-4121-481X
C RitchieSecciones Alergia Adultos y Pediátrica, Hospital Italiano de Buenos Aires Perón, Ciudad Autónoma de Buenos Aires, Argentina.
M RudenkoLondon Allergy and Immunology Centre, London, UK.
E KocatürkUrticaria Center of Reference and Excellence (UCARE), Institute of Allergology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
R F J CriadoDepartment of Dermatology, faculdade de medicina do ABC, Santo André, Brazil.ORCID https://orcid.org/0000-0003-2482-3047
S GregoriouFirst Department of Dermatology and Veneorology, National and Kapodistrian University of Athens A Syggros Hospital, Athens, Greece.
T BobylevClinic for Dermatology, Elbe Klinikum Buxtehude, Buxtehude, Germany.
A KleinheinzClinic for Dermatology, Elbe Klinikum Buxtehude, Buxtehude, Germany.
S TakahagiDepartment of Dermatology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
M HideDepartment of Dermatology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
A M Giménez-ArnauDepartment of Dermatology, Hospital del Mar Research Institute. Universitat Pompeu Fabra de Barcelona, Barcelona, Spain.ORCID https://orcid.org/0000-0001-5434-7753
A SalmanDepartment of Dermatology, Marmara University School of Medicine, İstanbul, Turkey.ORCID https://orcid.org/0000-0002-6407-926X
R Oztas KaraDepartment of Dermatology, Sakarya University Faculty of Medicine, Sakarya, Turkey.
B S DikicierDepartment of Dermatology, Sakarya University Faculty of Medicine, Sakarya, Turkey.
M B A van DoornDepartment of Dermatology, Erasmus MC, Rotterdam, Netherlands.
S F ThomsenDepartment of Dermato-Venereology and Wound Healing Centre, University of Copenhagen, Bispebjerg Hospital, Copenhagen, Denmark.
J M P A van den ReekDepartment of Dermatology, Radboud University Medical Centre, Nijmegen, Netherlands.
H RöckmannDepartment of Dermatology/Allergology, University Medical Centre Utrecht, Utrecht, Netherlands.

Funding

Novartis Pharma
6 · The paper itself

Abstract

backgroundLong-term data on the effectiveness and safety of omalizumab for chronic inducible urticaria (CIndU) in large populations are lacking.

objectiveTo evaluate the effectiveness, safety, estimated omalizumab treatment duration and its predictors, as well as differences between CIndU subtypes, in a large long-term CIndU cohort.

methodsA multinational multicenter study was conducted at 14 specialized urticaria centres (UCAREs), including all CIndU patients ever treated with omalizumab from 2009 until July 2022. Kaplan-Meier survival and regression analyses were performed.

resultsAcross 234 CIndU patients (55% female; mean age 37 years), 76% (n = 178) had standalone CIndU and 24% (n = 56) had predominant CIndU plus minor CSU, with an observation period up to 13 years. Most CIndU patients (73%, n = 145/200 with available data on response) had complete/good response to omalizumab treatment, without significant differences between CIndU subtypes. Sixty-two (26%) patients discontinued omalizumab; due to well-controlled disease (47%, n = 29), ineffectiveness (34%, n = 21), side effects (3%, n = 2), combination of ineffectiveness and side effects (3%, n = 2) and other reasons (13%, n = 8). The median estimated omalizumab treatment duration exceeded 5 years (54% drug survival at 5 years) and was mostly determined by well-controlled disease. Higher age predicted a lower chance to discontinue omalizumab due to well-controlled disease (HR 0.969, 95%CI 0.945-0.995). CIndU subtype and presence of minor CSU were not related to response and time until omalizumab discontinuation for any reason.

conclusionOmalizumab is highly effective and safe in CIndU patients, with long estimated treatment duration mainly reflecting long disease duration. Our data show omalizumab's high potential as treatment in any subtype of CIndU and support its clinical use for these patients.

Indexed as

Anti-Allergic AgentsChronic Inducible UrticariaOmalizumabAdolescentAdultAgedFemaleHumansMaleMiddle AgedTreatment OutcomeYoung AdultAnti-Allergic AgentsOmalizumabangioedemachronic inducible urticariadrug survivalomalizumabpredictor

Identifiers

PMID39377745
PMCPMC11804303

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.