Omalizumab in Chronic Spontaneous Urticaria: A Brazilian Real-Life Experience

被引:27
作者
Ensina, Luis Felipe [1 ,2 ]
Rodrigues Valle, Solange Oliveira [3 ]
Juliani, Ana Paula
Galeane, Michel
dos Santos, Rosaly Vieira [4 ]
Arruda, Luisa Karla [5 ]
Lima Melo, Janaina Michelle [5 ]
de Souza, Patricia Karla [1 ]
Serpa, Faradiba Sarquis [6 ]
de Andrade, Djanira Martins [1 ]
Franca, Alfeu Tavares [3 ]
Campos, Regis Albuquerque [7 ]
Camelo-Nunes, Ines [1 ,2 ]
Sole, Dirceu [1 ]
机构
[1] Univ Fed Sao Paulo, Rua Barata Ribeiro 490,CJ 67, BR-01308000 Sao Paulo, SP, Brazil
[2] Univ Santo Amaro, Sao Paulo, Brazil
[3] Univ Fed Rio de Janeiro, Rio De Janeiro, Brazil
[4] Univ Fed Parana, Immunodennatol & Clin Immunol Res Ctr, BR-80060000 Curitiba, Parana, Brazil
[5] Univ Sao Paulo, Ribeirao Preto Med Sch, BR-14049 Ribeirao Preto, Brazil
[6] Escola Super Ciencias Santa Casa Misericordia Vit, Vitoria, ES, Brazil
[7] Univ Fed Bahia, BR-41170290 Salvador, BA, Brazil
关键词
Urticaria; Omalizumab; Treatment; EFFICACY; THERAPY;
D O I
10.1159/000444985
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Current guidelines on chronic spontaneous urticaria (CSU) suggest a treatment based on a 3-step approach that aims at total symptom control, starting with H1 antihistamines. However, a significant number of patients present an antihistamine-resistant urticaria that must be treated with an alternative third-line therapy such as omalizumab. Methods: Patients with a history of CSU who did not respond to treatment with high doses of modern antihistamines were treated with 150 or 300 mg of omalizumab every 4 weeks. The response to treatment was recorded as complete (CR), partial (PR) or no response. A dose adjustment was proposed according to response. Results: We treated 47 CSU patients with omalizumab (40 females), of whom 39.5% had evidence of autoimmunity. The average number of treatments was 11.4 (range 2-87). All patients had been refractory to high-dose modern antihistamines. A CR was seen in 84.6% of patients who started with 300 mg and in 60% of those who started with 150 mg. Only 1 patient had no response to both the 150- and 300-mg doses. In 6 of the PR patients with 150 mg, a higher dose of 300 mg was proposed and 4 had a CR. Four patients discontinued the treatment. No severe adverse events were reported in the patients who finished the study. Discussion: Although good results were seen in both groups, CR rates were higher in those under a high-dose initial treatment. Our data strongly suggest that the therapy should be individualized. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:121 / 124
页数:4
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