Morita Shinya, Fukuda Atsushi, Hoshino Kimiko, Nakamaru Yuji, Fujiwara Keishi, Suzuki Masanobu, Honma Aya, Nakazono Akira, Homma Akihiro
Department of Otolaryngology-Head and Neck Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Otol Neurotol. 2025 Oct 1;46(9):1109-1116. doi: 10.1097/MAO.0000000000004541.
The aims of this study were to evaluate the otologic features and outcomes of otitis media associated with eosinophilic granulomatosis with polyangiitis (EGPA) and validate the current treatment strategies, including systemic corticosteroid (CS) and immunosuppressants for new-onset cases and therapeutic targeting of interleukin (IL)-5 for recurrent cases.
Retrospective case series.
Tertiary referral center.
Patients with otitis media associated with EGPA were eligible for inclusion.
Systemic CS alone or a combination of systemic CS and intravenous cyclophosphamide (IVCY) was performed as induction therapy. Maintenance therapy with oral CS and immunosuppressant, such as rituximab, methotrexate, or azathioprine, was administered. Treatment with mepolizumab was performed at the time of relapse of major organ involvement in EGPA, exacerbation of asthma, and/or recurrence of ear, nose, and throat symptoms after remission induction.
Air- and bone-conduction pure-tone thresholds, overall survival rate, EGPA relapse rate, and otitis media recurrence rate.
Systemic CS-based induction therapy achieved remission in all patients with EGPA. In both the CS + IVCY and CS-alone groups, hearing thresholds in the remission and/or resolution phase were significantly better than those at initial presentation at all frequencies ( p < 0.01). The 5-year estimated relapse rate of major organ involvement was 29.2%, and the 5-year estimated recurrence rate of otitis media was 43.6%. All cases of recurrent otitis media treated with mepolizumab achieved improvement in otologic symptoms and subsequent reduction in maintenance CS dose. However, half of ears with recurrent otitis media showed repeated secretion and cessation of middle ear discharge and required additional topical CS treatment during mepolizumab administration.
Immunosuppressive treatment affords a good response to systemic manifestations as well as otitis media associated with EGPA. Meanwhile, a significant proportion of patients experienced exacerbation of otitis media during maintenance therapy. Mepolizumab might be the treatment of choice for recurrent cases.
本研究旨在评估与嗜酸性肉芽肿性多血管炎(EGPA)相关的中耳炎的耳科特征及治疗结果,并验证当前的治疗策略,包括针对新发病例的全身用糖皮质激素(CS)和免疫抑制剂,以及针对复发病例的白细胞介素(IL)-5靶向治疗。
回顾性病例系列研究。
三级转诊中心。
符合条件的与EGPA相关的中耳炎患者。
单独使用全身用CS或全身用CS与静脉注射环磷酰胺(IVCY)联合作为诱导治疗。给予口服CS和免疫抑制剂(如利妥昔单抗、甲氨蝶呤或硫唑嘌呤)进行维持治疗。在EGPA主要器官受累复发、哮喘加重和/或缓解诱导后耳鼻喉症状复发时,使用美泊利单抗进行治疗。
气导和骨导纯音听阈、总生存率、EGPA复发率和中耳炎复发率。
基于全身用CS的诱导治疗使所有EGPA患者病情缓解。在CS + IVCY组和单独使用CS组中,缓解期和/或消退期的听力阈值在所有频率上均显著优于初始就诊时(p < 0.01)。主要器官受累的5年估计复发率为29.2%,中耳炎的5年估计复发率为43.6%。所有接受美泊利单抗治疗的复发性中耳炎病例的耳科症状均得到改善,随后维持CS剂量减少。然而,一半复发性中耳炎患者的耳朵出现中耳反复积液和积液停止的情况,在使用美泊利单抗治疗期间需要额外的局部CS治疗。
免疫抑制治疗对EGPA的全身表现以及相关中耳炎有良好疗效。同时,相当一部分患者在维持治疗期间中耳炎病情加重。美泊利单抗可能是复发性病例的首选治疗药物。