Watanabe Haruka, Takahagi Shunsuke, Hayama Koremasa, Fukunaga Atsushi, Nakagawa Yukinobu, Inomata Naoko, Chinuki Yuko, Hide Michihiro
Department of Dermatology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Department of Dermatology, JA Hiroshima General Hospital, Hiroshima, Japan.
Int J Dermatol. 2025 Feb;64(2):349-358. doi: 10.1111/ijd.17547. Epub 2024 Nov 3.
Chronic spontaneous urticaria (CSU) exhibits notable responsiveness to omalizumab (OMA). The prognosis and subsequent therapeutic strategies warrant comprehensive exploration in cases exhibiting inadequate responses to OMA.
We conducted a multicenter retrospective analysis to investigate the 12-month prognosis of patients inadequately responding to three injections of OMA. The endpoints encompassed identifying predictive factors for a favorable prognosis and assessing interventions related to an ameliorated prognostic outlook.
The study involved 48 patients who met the inclusion criteria. After three OMA administrations, therapeutic interventions included the continuation of OMA in 34 patients, systemic corticosteroids in seven patients, and immunosuppressants in 12 patients. After 12 months, 28 of the 48 patients exhibited a good prognosis, whereas the remaining 20 displayed a less favorable prognosis. Good prognostic determinants encompassed the duration of CSU within 51 weeks, the presence of angioedema, IgE levels ≤100 IU/mL pre-OMA, blood eosinophil counts ≥100/mm post-OMA, and urticaria control test (UCT) scores ≥5 pre-OMA and ≥6 post-OMA. Following the third OMA injection, the implementation of immunosuppressants presented an association with a good prognosis, while the employment of systemic corticosteroids correlated with an unfavorable prognosis.
More than half of patients inadequately responding to OMA achieved a good prognosis 12 months later. Several clinical variables appear to be predictive of prognosis, and certain therapeutic agents can be associated with prognostic outcomes.
慢性自发性荨麻疹(CSU)对奥马珠单抗(OMA)表现出显著的反应性。对于OMA反应不足的病例,其预后及后续治疗策略值得全面探索。
我们进行了一项多中心回顾性分析,以研究对三次OMA注射反应不足的患者的12个月预后。终点包括确定良好预后的预测因素以及评估与改善预后相关的干预措施。
该研究纳入了48例符合纳入标准的患者。三次OMA给药后,治疗干预措施包括34例患者继续使用OMA,7例患者使用全身皮质类固醇,12例患者使用免疫抑制剂。12个月后,48例患者中有28例预后良好,其余20例预后较差。良好预后的决定因素包括CSU病程在51周内、存在血管性水肿、OMA治疗前IgE水平≤100 IU/mL、OMA治疗后血嗜酸性粒细胞计数≥100/mm以及OMA治疗前荨麻疹控制试验(UCT)评分≥5且治疗后≥6。第三次OMA注射后,使用免疫抑制剂与良好预后相关,而使用全身皮质类固醇与不良预后相关。
超过一半对OMA反应不足的患者在12个月后预后良好。几个临床变量似乎可预测预后,某些治疗药物可能与预后结果相关。