Severe Asthma Unit, Allergy Department, Hospital Clinic Barcelona, FRCB-IDIBAPS, Barcelona, Catalonia, Spain; CIBER of Respiratory Diseases (CIBERES), Madrid, Spain.
Center for Rhinology and Allergology, Wiesbaden, Germany; Department of Otolaryngoloy, Head and Neck Surgery, Universitätsmedizin Mainz, Mainz, Germany.
J Allergy Clin Immunol Pract. 2024 Nov;12(11):2934-2944. doi: 10.1016/j.jaip.2024.09.012. Epub 2024 Sep 19.
The classic approach of nonsteroidal anti-inflammatory drug (NSAID)-exacerbated respiratory disease (NSAID-ERD) includes pharmaceutical and surgical treatments, as well as avoidance of cyclooxygenase 1-inhibitor NSAIDs. The introduction of biologics in the treatment of severe asthma and chronic rhinosinusitis with nasal polyps represents an alternative therapeutic approach to the classical aspirin therapy after desensitization (ATAD) in some regions, and with convincing results. However, their use is limited due to approval and/or high-cost restrictions. NSAID-ERD is a mainly type 2 and highly eosinophilic disease, and mAbs targeting IgE or IL-5, IL-4, and IL-13 have been shown to be effective for both severe asthma and severe chronic rhinosinusitis with nasal polyps. So far, dupilumab demonstrated greater efficacy in patients with NSAID-ERD than in aspirin-tolerant patients with regard to several clinical outcomes. Patients with NSAID-ERD respond very rapidly to omalizumab also, with reduction in the release of prostaglandin D and cysteinyl leukotrienes. Patients favored biologic treatment over ATAD in multiple retrospective analyses, which must be acknowledged when choosing one or the other option. Although this review will summarize ATAD in general, it will more prominently focus on when ATAD should be considered, even when type 2 biologics are available. In addition, there are conflicting studies as to whether patients on a type 2 biologic become desensitized to NSAIDs, because omalizumab proved to restore tolerance to aspirin in only two-third of patients. This goal of NSAID tolerance should be considered as part of disease control future approaches, representing one of many aspects in a patient-centered care approach.
经典的非甾体抗炎药(NSAID)加重的呼吸道疾病(NSAID-ERD)治疗方法包括药物和手术治疗,以及避免使用环氧化酶 1 抑制剂 NSAIDs。在一些地区,生物制剂在严重哮喘和慢性鼻-鼻窦炎伴鼻息肉的治疗中代表了经典阿司匹林脱敏治疗(ATAD)的另一种治疗方法,并且取得了令人信服的效果。然而,由于批准和/或高成本限制,它们的使用受到限制。NSAID-ERD 主要是 2 型和高度嗜酸性粒细胞疾病,靶向 IgE 或 IL-5、IL-4 和 IL-13 的 mAb 已被证明对严重哮喘和严重慢性鼻-鼻窦炎伴鼻息肉均有效。迄今为止,与阿司匹林耐受患者相比,dupilumab 在 NSAID-ERD 患者中显示出在多个临床结局方面更有效。奥马珠单抗也能使 NSAID-ERD 患者迅速做出反应,降低前列腺素 D 和半胱氨酰白三烯的释放。在多项回顾性分析中,患者更喜欢生物治疗而不是 ATAD,在选择一种或另一种方案时必须承认这一点。尽管本综述将一般性地总结 ATAD,但更侧重于何时应考虑 ATAD,即使有 2 型生物制剂可用。此外,关于接受 2 型生物制剂治疗的患者是否对 NSAIDs 脱敏存在相互矛盾的研究,因为奥马珠单抗仅在三分之二的患者中证明可恢复对阿司匹林的耐受性。这种对 NSAID 耐受性的目标应被视为未来疾病控制方法的一部分,代表患者为中心的护理方法的众多方面之一。