Kasperska-Zajac A, Jarząb J, Żerdzińska A, Bąk K, Grzanka A
Department of Internal Diseases, Dermatology and Allergology in Zabrze, SMDZ in Zabrze, Medical University of Silesia in Katowice, Poland
Department of Internal Diseases, Dermatology and Allergology in Zabrze, SMDZ in Zabrze, Medical University of Silesia in Katowice, Poland.
Int J Immunopathol Pharmacol. 2016 Jun;29(2):320-8. doi: 10.1177/0394632015623795. Epub 2016 Jan 4.
Despite the excellent efficacy and safety profile of omalizumab in chronic spontaneous urticaria (CSU), there are scarce data concerning its role in the treatment of refractory cases with different phenotypes of urticaria. We describe our experience with the therapy of nine patients with CSU co-existing with delayed pressure urticaria (DPU) or angioedema or both and refractory to treatment with high-dose antihistamines. The first patient, with severe CSU and recurrent angioedema, did not respond well to cyclosporine A or corticosteroids and suffered from numerous side effects of long-term corticosteroid therapy. The second patient presented with severe symptoms of DPU, which first of all prevented any daily activities of the professional routines. Both patients showed a complete remission of urticaria after the first injection of omalizumab. The third patient with CSU and severe DPU had been ineffectively treated for more than 20 years with various medications. Following the administration of omalizumab, the symptoms of CSU subsided but those of DPU intensified, and the drug was withdrawn after two cycles. In another four patients with refractory CSU and angioedema, the symptoms subsided after the first administration of omalizumab, and the patients have been in remission for about 5 weeks. In the remaining two patients, the symptoms did not resolve despite four 300 mg doses of omalizumab. It is important to establish a therapeutic regimen with omalizumab (150-300 mg; every 4-8 weeks) tailored to individual patient's needs and dependent on the type of urticaria; this may minimize unnecessary the medication exposure, adverse drug effects, and healthcare costs.
尽管奥马珠单抗在慢性自发性荨麻疹(CSU)的治疗中具有出色的疗效和安全性,但关于其在治疗不同表型难治性荨麻疹中的作用的数据却很少。我们描述了我们对9例CSU合并迟发性压力性荨麻疹(DPU)或血管性水肿或两者兼有且对高剂量抗组胺药治疗无效的患者进行治疗的经验。首例患者患有严重的CSU和复发性血管性水肿,对环孢素A或皮质类固醇反应不佳,并长期接受皮质类固醇治疗,出现了许多副作用。第二例患者表现出严重的DPU症状,这首先妨碍了其日常工作中的任何活动。两名患者在首次注射奥马珠单抗后荨麻疹均完全缓解。第三例患有CSU和严重DPU的患者用各种药物治疗20多年均无效。使用奥马珠单抗后,CSU症状消退,但DPU症状加重,两个疗程后停用该药。另外4例难治性CSU和血管性水肿患者在首次使用奥马珠单抗后症状消退,且已缓解约5周。其余2例患者尽管使用了4剂300mg的奥马珠单抗,症状仍未缓解。重要的是要根据个体患者的需求并取决于荨麻疹的类型制定奥马珠单抗(150 - 300mg;每4 - 8周一次)的治疗方案;这可以最大程度地减少不必要的药物暴露、药物不良反应和医疗费用。