Chapman Kenneth R, Cartier Andre, Hébert Jacques, McIvor R Andrew, Schellenberg R Robert
University of Toronto, Toronto, Ontario, Canada.
Can Respir J. 2006 Jul-Aug;13 Suppl B(Suppl B):1B-9B. doi: 10.1155/2006/279435.
A novel anti-immunoglobulin E (anti-IgE) therapy for asthma, omalizumab, has been approved for use in Canada.
To review the basic and clinical data for omalizumab, and to examine its possible role for asthma management in Canada.
A literature search from 1960 to 2006 was conducted in MEDLINE to identify studies of omalizumab. In addition, abstracts from recent respiratory and allergy scientific meetings were sought, and any unpublished data were requested from the manufacturer. A consensus panel of respiratory and allergy specialists reviewed and summarized the data, and derived a set of recommendations for omalizumab use.
Omalizumab is a humanized monoclonal antibody designed to bind to the C epsilon 3 domain of the IgE molecule, forming soluble immune complexes that are cleared by the reticuloendothelial system. Subcutaneous injections, given at two- or four-week intervals at the recommended dose, result in a rapid decrease in free circulating IgE levels. In two phase III clinical trials of 1405 adult and adolescent patients with moderate to severe asthma maintained on moderate doses of inhaled corticosteroids (ICS), omalizumab reduced exacerbation rates compared with placebo, and was associated with improved symptoms and a greater corticosteroid-sparing effect. In a trial of 419 patients with severe disease that was uncontrolled despite the use of high-dose ICS and concurrent long-acting beta2-agonists, severe exacerbations were 50% less frequent in omalizumab-treated patients than in control subjects. Retrospective analyses have identified the characteristics of patients most likely to respond to omalizumab treatment.
Omalizumab may be considered as a potential adjunctive therapy in atopic patients with severe asthma uncontrolled by conventional therapy with optimal doses of ICS and appropriate adjunctive therapy (eg, long-acting beta2-agonists). Typically, patients are identified by the need for frequent short course or continuous oral corticosteroids. Therapy should be initiated only after review by a specialist to confirm the diagnosis and that conventional therapy is optimal.
一种用于治疗哮喘的新型抗免疫球蛋白E(抗IgE)疗法——奥马珠单抗,已在加拿大获批使用。
回顾奥马珠单抗的基础和临床数据,并探讨其在加拿大哮喘管理中的可能作用。
在MEDLINE数据库中进行了1960年至2006年的文献检索,以识别有关奥马珠单抗的研究。此外,还查找了近期呼吸和过敏科学会议的摘要,并向制造商索取了任何未发表的数据。由呼吸和过敏专家组成的共识小组对数据进行了审查和总结,并得出了一套关于奥马珠单抗使用的建议。
奥马珠单抗是一种人源化单克隆抗体,旨在与IgE分子的Cε3结构域结合,形成可被网状内皮系统清除的可溶性免疫复合物。按照推荐剂量每两周或四周进行一次皮下注射,可使游离循环IgE水平迅速下降。在两项针对1405例成年和青少年中重度哮喘患者的III期临床试验中,这些患者均维持使用中等剂量的吸入性糖皮质激素(ICS),与安慰剂相比,奥马珠单抗降低了病情加重率,并改善了症状,且具有更大的糖皮质激素节省效应。在一项针对419例严重哮喘患者的试验中,尽管使用了高剂量ICS和联合长效β2受体激动剂,但病情仍未得到控制,接受奥马珠单抗治疗的患者严重病情加重的频率比对照组低50%。回顾性分析确定了最有可能对奥马珠单抗治疗产生反应的患者特征。
对于经最佳剂量ICS和适当辅助治疗(如长效β2受体激动剂)的常规治疗无法控制的重度特应性哮喘患者,可考虑将奥马珠单抗作为一种潜在的辅助治疗方法。通常,需要频繁短期或持续口服糖皮质激素的患者符合条件。仅在专科医生复查以确认诊断且常规治疗已达最佳效果后,方可开始治疗。