Capital Allergy and Respiratory Disease Center, Sacramento, Calif.
Department of Pediatrics, University of North Texas, Fort Worth, Tex.
J Allergy Clin Immunol. 2017 May;139(5):1431-1444. doi: 10.1016/j.jaci.2017.03.002.
Asthma is one of the most common chronic diseases of childhood. Allergen sensitization and high frequencies of comorbid allergic diseases are characteristic of severe asthma in children. Omalizumab, an anti-IgE mAb, is the first targeted biologic therapeutic approved for the treatment of moderate-to-severe persistent allergic asthma (AA) that remains uncontrolled despite high-dose inhaled corticosteroids plus other controller medications. Since its initial licensing for use in adults and adolescents 12 years of age and older, the clinical efficacy, safety, and tolerability of omalizumab have been demonstrated in several published clinical trials in children aged 6 to less than 12 years with moderate-to-severe AA. These studies supported the approval of the pediatric indication (use in children aged ≥6 years) by the European Medicines Agency in 2009 and the US Food and Drug Administration in 2016. After this most recent change in licensing, we review the outcomes from clinical trials in children with persistent AA receiving omalizumab therapy and observational studies from the past 7 years of clinical experience in Europe. Data sources were identified by using PubMed in 2016. Guidelines and management recommendations and materials from the recent US Food and Drug Administration's Pediatric Advisory Committee meeting are also reviewed.
哮喘是儿童最常见的慢性疾病之一。变应原致敏和合并过敏疾病的高频率是儿童重度哮喘的特征。奥马珠单抗是一种抗 IgE mAb,是首个获批用于治疗中重度持续性过敏性哮喘(AA)的靶向生物治疗药物,即使在高剂量吸入皮质激素加其他控制药物治疗下仍未得到控制。自最初批准用于 12 岁及以上成人和青少年以来,奥马珠单抗在几项已发表的临床试验中已显示出在 6 岁至 12 岁以下中重度 AA 儿童中的临床疗效、安全性和耐受性。这些研究支持了欧洲药品管理局在 2009 年和美国食品和药物管理局在 2016 年批准儿科适应证(用于≥6 岁儿童)。在最近的许可变更后,我们回顾了接受奥马珠单抗治疗的持续性 AA 儿童临床试验结果和过去 7 年欧洲的临床经验观察性研究。在 2016 年使用 PubMed 确定了数据来源。还回顾了最近美国食品和药物管理局儿科咨询委员会会议的指南和管理建议以及材料。