Unmet Needs in Treatment Escalation for Chronic Spontaneous Urticaria: Findings From the CURE Registry

dc.contributor.authorKolkhir P.
dc.contributor.authorSalameh P.
dc.contributor.authorZajac M.
dc.contributor.authorKasperska-Zajac A.
dc.contributor.authorGiménez-Arnau A.
dc.contributor.authorPuertolas M.
dc.contributor.authorBonnekoh H.
dc.contributor.authorVera Ayala C.
dc.contributor.authorMakris M.
dc.contributor.authorChatzidimitriou E.
dc.contributor.authorGregoriou S.
dc.contributor.authorKulthanan K.
dc.contributor.authorBauer A.
dc.contributor.authorBizjak-Suran M.
dc.contributor.authorFomina D.
dc.contributor.authorBocquet A.
dc.contributor.authorDissemond J.
dc.contributor.authorAbuzakouk M.
dc.contributor.authorRaftery T.
dc.contributor.authorChapman-Rothe N.
dc.contributor.authorKocatürk E.
dc.contributor.authorGrattan C.
dc.contributor.authorAsero R.
dc.contributor.authorPeter J.G.
dc.contributor.authorThomsen S.F.
dc.contributor.authorWeller K.
dc.contributor.correspondenceKolkhir P.
dc.contributor.otherMahidol University
dc.date.accessioned2026-02-06T18:26:07Z
dc.date.available2026-02-06T18:26:07Z
dc.date.issued2026-01-01
dc.description.abstractBackground: Many patients with chronic spontaneous urticaria (CSU) remain symptomatic despite receiving second-generation H<inf>1</inf>-antihistamines (sgH<inf>1</inf>-AH). This data analysis from the Chronic Urticaria Registry (CURE) aimed to describe treatment patterns and identify unmet needs in real-world practice. Methods: CURE is an international, prospective registry of patients with chronic urticaria. Treatment responses were categorized as Urticaria Control Test (UCT) changes from baseline (BL) to 6-month follow-up (FU). Complete response was defined as UCT = 16 with a ≥ 3-point increase. Results: Data were available from 3995 adult patients with CSU at BL and 1288 at FU with evaluable UCT. After treatment escalation from BL to FU, 5.3% (no treatment to licensed-dose sgH<inf>1</inf>-AH), 6.0% (licensed-dose sgH<inf>1</inf>-AH to up-dosed sgH<inf>1</inf>-AH), and 28.4% (any dose sgH<inf>1</inf>-AH to omalizumab) achieved complete response. Factors associated with a lower probability of treatment escalation at FU were UCT ≥ 12 and omalizumab treatment at BL (both p < 0.0001). About one-third (28.6%) of patients clinically eligible for escalation at BL (UCT < 12) did not receive step-up treatment (18.0%) or were even stepped down (10.6%) and remained poorly controlled at FU. Factors associated with lack of escalation in this group included younger age (p = 0.014), shorter disease duration (p = 0.071), presence of wheals and angioedema (p = 0.002), better quality of life (p = 0.001), and treatment with up-dosed sgH<inf>1</inf>-AH (p = 0.031). Conclusion: Appropriate treatment escalation improves CSU control, although only about a quarter of patients achieve a complete response, indicating the need for novel treatments. Many patients with poorly controlled CSU do not receive guideline-recommended treatment escalation and remain symptomatic on their current treatments, which deserves further attention.
dc.identifier.citationAllergy European Journal of Allergy and Clinical Immunology (2026)
dc.identifier.doi10.1111/all.70199
dc.identifier.eissn13989995
dc.identifier.issn01054538
dc.identifier.pmid41532642
dc.identifier.scopus2-s2.0-105027513884
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/114658
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.subjectImmunology and Microbiology
dc.titleUnmet Needs in Treatment Escalation for Chronic Spontaneous Urticaria: Findings From the CURE Registry
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105027513884&origin=inward
oaire.citation.titleAllergy European Journal of Allergy and Clinical Immunology
oairecerif.author.affiliationKøbenhavns Universitet
oairecerif.author.affiliationCharité – Universitätsmedizin Berlin
oairecerif.author.affiliationNational and Kapodistrian University of Athens
oairecerif.author.affiliationUniversität Duisburg-Essen
oairecerif.author.affiliationSechenov First Moscow State Medical University
oairecerif.author.affiliationUniversitat Pompeu Fabra Barcelona
oairecerif.author.affiliationNovartis International AG
oairecerif.author.affiliationSlaski Uniwersytet Medyczny w Katowicach
oairecerif.author.affiliationUniverza v Mariboru
oairecerif.author.affiliationGuy's Hospital
oairecerif.author.affiliationUniversitätsklinikum Carl Gustav Carus Dresden
oairecerif.author.affiliationCentre Hospitalier Universitaire de Grenoble
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationBispebjerg Hospital
oairecerif.author.affiliationUniversité Libanaise
oairecerif.author.affiliationGroote Schuur Hospital
oairecerif.author.affiliationBahçeşehir Üniversitesi
oairecerif.author.affiliationUniverza v Ljubljani Medicinska Fakulteta
oairecerif.author.affiliationMoscow Healthcare Department
oairecerif.author.affiliationCleveland Clinic Abu Dhabi
oairecerif.author.affiliationUniversity of Nicosia Medical School
oairecerif.author.affiliationAstana Medical University
oairecerif.author.affiliationFraunhofer Institute for Translational Medicine and Pharmacology ITMP
oairecerif.author.affiliationGilbert and Rose-Marie Chagoury School of Medicine
oairecerif.author.affiliationInstitut National de Santé Publique, d’Épidémiologie Clinique et de Toxicologie-Liban
oairecerif.author.affiliationUniversity of Cape Town Lung Institute
oairecerif.author.affiliationBolnišnica Golnik
oairecerif.author.affiliationNovartis Ireland Limited
oairecerif.author.affiliationClinica San Carlo

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