Menzella Francesco, Just Jocelyne, Sauerbeck Inessa Schwab, Mailaender Claudia, Saccheri Fabiana, Thonnelier Celine, Jaumont Xavier, Mala Laurence
Head, Pulmonology Unit, S. Valentino Hospital, AULSS 2 Marca Trevigiana, Italy.
Allergology Department, Trousseau Hospital, AP-HP Paris, France.
World Allergy Organ J. 2023 Jun 10;16(6):100787. doi: 10.1016/j.waojou.2023.100787. eCollection 2023 Jun.
Immunoglobulin E (IgE) plays a critical role in the allergen-initiated inflammatory pathway and thus serves as a viable therapeutic target in allergic or IgE-mediated diseases such as asthma. Omalizumab, an -IgE biologic, has been approved in the United States (US, 2003) and in the European Union (EU, 2005) as an add-on therapy in patients with moderate-to-severe persistent asthma and severe allergic asthma (SAA) aged 6 years and older. The dose and frequency of omalizumab are adjusted based on the patient's body weight and baseline IgE levels, as recommended by its dosing tables. Currently, these dosing recommendations are limited to patients with baseline IgE levels of up to 1500 IU/mL in the European Union and 700 IU/mL in the United States. However, many patients with SAA have IgE levels >1500 IU/mL, highlighting an unmet need. This review presents the current evidence on the treatment benefits of omalizumab in patients with IgE levels >1500 IU/mL. The findings from the reviewed studies which included >3000 patients support the efficacy and effectiveness of omalizumab in reducing exacerbations, and improving asthma control, lung function, and quality of life in patients with severe asthma having IgE levels beyond the current dosing range. Omalizumab was well-tolerated in these patients, with no new safety signals. In addition, high IgE levels (>1500 IU/mL) are also reported in several comorbidities of asthma (allergic rhinitis, atopic dermatitis, allergic bronchopulmonary aspergillosis [ABPA], food allergy, and nasal polyposis) and omalizumab has demonstrated efficacy and safety in these indications. These data suggest that omalizumab may be considered for administration in SAA patients, with high IgE levels outside the current dosing tables. A detailed assessment of patients with high IgE levels is needed before deciding on the optimal treatment approach. A management algorithm for SAA patients with IgE >1500 IU/mL is proposed in this review and a suggestion to follow the Delphi consensus is advised.
免疫球蛋白E(IgE)在变应原引发的炎症途径中起关键作用,因此在哮喘等过敏性或IgE介导的疾病中是一个可行的治疗靶点。奥马珠单抗是一种抗IgE生物制剂,已在美国(2003年)和欧盟(2005年)获批,用于6岁及以上中重度持续性哮喘和重度过敏性哮喘(SAA)患者的附加治疗。奥马珠单抗的剂量和给药频率根据患者体重和基线IgE水平进行调整,如给药表所推荐。目前,这些给药建议仅限于欧盟基线IgE水平高达1500 IU/mL和美国基线IgE水平高达700 IU/mL的患者。然而,许多SAA患者的IgE水平>1500 IU/mL,这凸显了未满足的需求。本综述介绍了奥马珠单抗治疗IgE水平>1500 IU/mL患者的现有证据。纳入3000多名患者的综述研究结果支持奥马珠单抗在降低重度哮喘患者(其IgE水平超出当前给药范围)的病情加重、改善哮喘控制、肺功能和生活质量方面的疗效和有效性。奥马珠单抗在这些患者中耐受性良好,没有新的安全信号。此外,在哮喘的几种合并症(过敏性鼻炎、特应性皮炎、变应性支气管肺曲霉病[ABPA]、食物过敏和鼻息肉病)中也报告了高IgE水平(>1500 IU/mL),奥马珠单抗在这些适应症中已证明具有疗效和安全性。这些数据表明,对于IgE水平高于当前给药表范围的SAA患者,可考虑使用奥马珠单抗。在决定最佳治疗方法之前,需要对高IgE水平患者进行详细评估。本综述提出了IgE>1500 IU/mL的SAA患者的管理算法,并建议遵循德尔菲共识。