Department of Dermatology, Chung-Ang University College of Medicine, Seoul, Korea.
Clin Exp Dermatol. 2013 Jul;38(5):496-500. doi: 10.1111/j.1365-2230.2012.04438.x. Epub 2012 Oct 22.
Atopic dermatitis (AD) is a chronic and relapsing inflammatory skin disease affecting > 10% of children and 1-3% of adults, and can cause significant morbidity. The incidence of AD seems to be increasing. Omalizumab, a monoclonal antibody, has recently been suggested as a potential new systemic treatment for patients with recalcitrant AD with elevated IgE levels, based on its efficacy in treating asthma and allergic rhinitis. We report a study of 10 patients with AD (aged 19-35 years) who received anti-IgE treatment for persistent asthma. All patients, regardless of IgE value, were treated with a fixed schedule of eight cycles of omalizumab 300 mg administered subcutaneously at intervals of 2 weeks. Eczema symptoms were scored at baseline and after 2, 4 and 6 months of treatment. There was a steady improvement in the objective SCORAD (SCORing Atopic Dermatitis), with significantly lower scores observed at the 6-month evaluation. At 2 months after the end of treatment, two patients had a very good result (SCORAD reduction of > 50%), five patients had a satisfactory result (reduction of 25-50%), and three patients had no clinically relevant result (reduction of 25-50%). No patient had worsening of the AD (increase of > 25% in SCORAD), and once a clinical improvement occurred, none of the patients experienced worsening of their eczema symptoms while on omalizumab. With the caveats of the financial expense and unknown long-term risks of malignancy associated with omalizumab, this drug should be considered for treatment-resistant patients with AD, particularly patients with high IgE level whose symptoms are not controlled by routine therapies. Omalizumab has proven useful in treating asthma, but it may also prove valuable for other conditions, such as allergic rhinitis, food allergies, chronic urticaria, and AD, as shown by the present study.
特应性皮炎(AD)是一种影响> 10%儿童和 1-3%成年人的慢性复发性炎症性皮肤病,可导致显著的发病率。AD 的发病率似乎在增加。奥马珠单抗是一种单克隆抗体,最近基于其在治疗哮喘和过敏性鼻炎方面的疗效,被提议作为一种潜在的新的全身性治疗方法,用于治疗特应性皮炎患者,这些患者 IgE 水平升高,且病情顽固。我们报告了一项对 10 名患有特应性皮炎(年龄 19-35 岁)的患者的研究,这些患者因持续性哮喘接受了抗 IgE 治疗。所有患者,无论 IgE 值如何,均按照皮下注射奥马珠单抗 300mg 的固定方案接受治疗,每 2 周一次,共 8 个周期。在治疗前和治疗后 2、4 和 6 个月评估湿疹症状。客观的 SCORAD(特应性皮炎评分)持续改善,在 6 个月评估时,评分明显降低。在治疗结束后 2 个月,有 2 名患者出现非常好的结果(SCORAD 降低> 50%),5 名患者出现满意的结果(降低 25-50%),3 名患者无临床相关结果(降低 25-50%)。没有患者的 AD 恶化(SCORAD 增加> 25%),一旦出现临床改善,在使用奥马珠单抗期间,没有患者的湿疹症状恶化。奥马珠单抗治疗特应性皮炎,特别是那些常规治疗不能控制症状的高 IgE 水平的患者,具有潜在价值,但也需要考虑到该药的费用问题和潜在的长期恶性肿瘤风险。奥马珠单抗已被证明对治疗哮喘有用,但正如本研究所示,它对其他疾病,如过敏性鼻炎、食物过敏、慢性荨麻疹和特应性皮炎也可能具有价值。