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Omalizumab versus cyclosporin-A for the treatment of chronic spontaneous urticaria: can we define better-responding endotypes?
Kocatürk, Emek; Başkan, Emel Bülbül; Küçük, Özlem Su; Özdemir, Mustafa; Örnek, Sinem; Can, Pelin Kuteyla; Hașal, Eda; Engin, Burhan; Atakan, Nilgün; Alpsoy, Erkan.
Afiliação
  • Kocatürk, Emek; Koc University. School of Medicine. Department of Dermatology. Istanbul. TR
  • Başkan, Emel Bülbül; Uludag University. School of Medicine. Department of Dermatology. Bursa. TR
  • Küçük, Özlem Su; Bezmialem Vakif University. School of Medicine. Department of Dermatology. Istanbul. TR
  • Özdemir, Mustafa; Istanbul Medipol University. School of Medicine. Department of Dermatology. Istanbul. TR
  • Örnek, Sinem; Ankara Diskapi Yildirim Beyazit Training and Research Hospital. Department of Dermatology. Ankara. TR
  • Can, Pelin Kuteyla; VM Medical Park Maltepe Hospital. Department of Dermatology. Istanbul. TR
  • Hașal, Eda; Uludag University. School of Medicine. Department of Dermatology. Bursa. TR
  • Engin, Burhan; Istanbul University. Cerrahpasa School of Medicine. Department of Dermatology. Istanbul. TR
  • Atakan, Nilgün; Hacettepe University. School of Medicine. Department of Dermatology. Ankara. TR
  • Alpsoy, Erkan; Akdeniz University. School of Medicine, Antalya. Department of Dermatology. Antalya. TR
An. bras. dermatol ; 97(5): 592-600, Sept.-Oct. 2022. tab, graf
Article em En | LILACS-Express | LILACS | ID: biblio-1403153
Biblioteca responsável: BR1.1
ABSTRACT
Abstract

Background:

Chronic Spontaneous Urticaria (CSU) is characterized by recurrent wheals and/or angioedema for longer than 6-weeks. Guidelines recommend Omalizumab (Oma) as first-line and Cyclosporine-A (Cs-A) as second-line treatment in antihistamine resistant CSU. This step-wise algorithm might be time-consuming and costly.

Objective:

To determine indicators of response to Oma or Cs-A in CSU patients.

Methods:

We retrospectively analyzed data from seven centers in Turkey; the inclusion criteria for patients were to receive both Oma and Cs-A treatment (not concurrently) at some point in time during their follow-up. Clinical and laboratory features were compared between groups.

Results:

Among 110 CSU patients; 47 (42.7%) were Oma-responders, 15 (13.6%) were Cs-A-responders, and 24 (21.8%) were both Oma and Cs-A responders and 24 (21.8%) were non-responders to either drug. High CRP levels were more frequent in Cs-A-responders (72.7% vs. 40.3%; p = 0.055). Oma-responders had higher baseline UCT (Urticaria Control Test) scores (6 vs. 4.5; p = 0.045). Responders to both drugs had less angioedema and higher baseline UCT scores compared to other groups (33.3% vs. 62.8%; p = 0.01 and 8 vs. 5; p = 0.017). Non-responders to both drugs had an increased frequency in the female gender and lower baseline UCT scores compared to other groups (87.5% vs. 61.6%; p = 0.017 and 5 vs. 7; p = 0.06). Study

Limitations:

Retrospective nature, limited number of patients, no control group, the lack of the basophil activation (BAT) or BHRA (basophil histamine release assay) tests.

Conclusions:

Baseline disease activity assessment, which considers the presence of angioedema and disease activity scores, gender, and CRP levels might be helpful to predict treatment outcomes in CSU patients and to choose the right treatment for each patient. Categorizing patients into particular endotypes could provide treatment optimization and increase treatment success. © 2022 Published by Elsevier España, S.L.U. on behalf of Sociedade Brasileira de Dermatologia. This is an open access article under the CC BY license (https//creativecommons.org/licenses/by/4.0/).
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Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Tipo de estudo: Guideline / Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: LILACS Tipo de estudo: Guideline / Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article