Gershnabel Milk Dafna, Lam Kent K, Han Joseph K
Divisions of Rhinology, Endoscopic Skull Base Surgery, and Allergy, Department of Otolaryngology - Head Neck Surgery, Eastern Virginia Medical School, Norfolk, VA, USA.
Division of Rhinology, Department of Otolaryngology - Head Neck Surgery, Meir Medical Center, Kfar Saba, Israel.
Am J Rhinol Allergy. 2025 Jan;39(1):38-48. doi: 10.1177/19458924241280757. Epub 2024 Sep 15.
Temporary eosinophilia is a potential adverse reaction of monoclonal antibody therapies in the treatment of a variety of type 2 inflammatory conditions, including asthma and chronic rhinosinusitis with nasal polyposis (CRSwNP). The pathophysiology, epidemiology, and clinical significance of eosinophilia and eosinophilic adverse reactions following the initiation of biologic therapy are unclear.
To describe the postmarketing, eosinophilic adverse reactions with clinical significance in patients treated with the 3 biologic therapies approved by the U.S. Food and Drug Administration (FDA) for CRSwNP: dupilumab, omalizumab, and mepolizumab.
The FDA Adverse Event Reporting System (FAERS) Public Dashboard was searched for eosinophilic adverse reactions related to dupilumab, omalizumab, and mepolizumab treatments from November 2004 to December 2022. Data regarding each of the eosinophilic adverse reactions were extracted and analyzed.
A total of 218, 270, and 134 reports of eosinophilic adverse reactions were reported among patients who were treated with dupilumab, omalizumab, and mepolizumab, respectively. The most common eosinophilic adverse reaction was eosinophilic granulomatosis with polyangiitis (338 patients), followed by eosinophilic respiratory tract reactions (158 patients). The most common indication for biological treatment among the reaction groups was asthma.
Eosinophilic adverse reactions are rare but consequential complications of biological treatment. They are more common among patients treated for asthma and chronic rhinosinusitis with nasal polyposis. Measuring and monitoring blood eosinophil levels may be appropriate in specific clinical instances when patients are started on different biologic therapies for type 2 inflammatory conditions.
暂时性嗜酸性粒细胞增多是单克隆抗体疗法在治疗多种2型炎症性疾病(包括哮喘和伴有鼻息肉的慢性鼻-鼻窦炎(CRSwNP))时可能出现的不良反应。生物治疗开始后嗜酸性粒细胞增多及嗜酸性粒细胞不良反应的病理生理学、流行病学和临床意义尚不清楚。
描述美国食品药品监督管理局(FDA)批准用于治疗CRSwNP的3种生物疗法(度普利尤单抗、奥马珠单抗和美泊利单抗)治疗患者中具有临床意义的上市后嗜酸性粒细胞不良反应。
在FDA不良事件报告系统(FAERS)公共仪表盘上搜索2004年11月至2022年12月期间与度普利尤单抗、奥马珠单抗和美泊利单抗治疗相关的嗜酸性粒细胞不良反应。提取并分析每种嗜酸性粒细胞不良反应的数据。
分别接受度普利尤单抗、奥马珠单抗和美泊利单抗治疗的患者中,共报告了218例、270例和134例嗜酸性粒细胞不良反应报告。最常见的嗜酸性粒细胞不良反应是嗜酸性肉芽肿性多血管炎(338例患者),其次是嗜酸性呼吸道反应(158例患者)。反应组中生物治疗最常见的适应证是哮喘。
嗜酸性粒细胞不良反应是生物治疗罕见但严重的并发症。在接受哮喘和伴有鼻息肉的慢性鼻-鼻窦炎治疗的患者中更为常见。在患者开始使用不同生物疗法治疗2型炎症性疾病的特定临床情况下,测量和监测血液嗜酸性粒细胞水平可能是合适的。