Similar Efficacy with Omalizumab in Chronic Idiopathic/Spontaneous Urticaria Despite Different Background Therapy

被引:61
作者
Casale, Thomas B. [1 ]
Bernstein, Jonathan A. [2 ,3 ]
Maurer, Marcus [4 ]
Saini, Sarbjit S. [5 ]
Trzaskoma, Benjamin [6 ]
Chen, Hubert [6 ]
Grattan, Clive E. [7 ]
Gimenez-Arnau, Ana [8 ]
Kaplan, Allen P. [9 ,10 ]
Rosen, Karin [6 ]
机构
[1] Univ S Florida, Dept Med, Div Allergy & Immunol, Tampa, FL USA
[2] Univ Cincinnati, Dept Internal Med, Cincinnati, OH USA
[3] Univ Cincinnati, Div Immunol, Allergy Sect, Cincinnati, OH USA
[4] Charite, Dept Dermatol & Allergy, D-13353 Berlin, Germany
[5] Johns Hopkins Asthma & Allergy Ctr, Div Allergy & Clin Immunol, Baltimore, MD USA
[6] Genentech Inc, 1 DNA Way, San Francisco, CA 94080 USA
[7] Norfolk & Norwich Univ Hosp, Dept Dermatol, Norwich, Norfolk, England
[8] Univ Autonoma Barcelona, Dept Dermatol, Inst Mar Invest Med, E-08193 Barcelona, Spain
[9] Med Univ S Carolina, Dept Med, Div Pulm & Crit Care, Charleston, SC 29425 USA
[10] Med Univ S Carolina, Allergy & Clin Immunol, Charleston, SC 29425 USA
关键词
Omalizumab; Urticaria; Chronic spontaneous; Chronic idiopathic; Itch; Hive; Pruritus; Wheal; Antihistamine; MANAGEMENT; IGE; DEFINITION; DIAGNOSIS; PSORIASIS; ANTIBODY; MODERATE;
D O I
10.1016/j.jaip.2015.04.015
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
BACKGROUND: Data from the 3 omalizumab pivotal trials in patients with chronic idiopathic urticaria/chronic spontaneous urticaria (CIU/CSU) represent the largest database of patients reported to date with refractory disease (omalizumab, n = 733; placebo, n = 242). OBJECTIVE: The objective of this study was to compare results from ASTERIA I and II, which included only approved doses of H-1-antihistamine as background therapy based on regulatory authority requirements, to those from GLACIAL, which permitted higher doses of H-1-antihistamines as well as other types of background therapy, in a post hoc analysis. METHODS: Efficacy data from the placebo, omalizumab 150-mg, and omalizumab 300-mg treatment arms of ASTERIA I and II were pooled and analyzed (n = 162 and n = 160, respectively). The 300-mg treatment arm analyses were compared with the analysis of data from GLACIAL (n = 252) using analysis of covariance models. The key efficacy endpoint was change from baseline to week 12 in mean weekly itch severity score (ISS); other endpoints were also evaluated. Safety data were pooled from all 3 studies. RESULTS: Mean ISS was significantly reduced from baseline at week 12 in the pooled ASTERIA I and II omalizumab 150- and 300-mg treatment arms and in the GLACIAL omalizumab 300-mg arm. The weekly ISS reduction magnitude at week 12 was similar between the omalizumab 300-mg groups in the ASTERIA I and II pooled and GLACIAL studies. Similar treatment effect sizes were observed across multiple endpoints. Omalizumab was well tolerated and the adverse-event profile was similar regardless of background therapy for CIU/CSU. The overall safety profile was generally consistent with omalizumab therapy in allergic asthma. CONCLUSION: Omalizumab 300 mg was safe and effective in reducing CIU/CSU symptoms regardless of background therapy. (C) 2015 The Authors. Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology.
引用
收藏
页码:743 / +
页数:9
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