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奥马珠单抗治疗非过敏性重症哮喘的疗效。

Effectiveness of omalizumab in non-allergic severe asthma.

机构信息

Servei de Pneumologia, Corporacio Sanitaria Parc Tauli, Sabadell Barcelona, Spain.

出版信息

J Biol Regul Homeost Agents. 2013 Jan-Mar;27(1):45-53.

Abstract

Omalizumab is an effective drug for allergic asthma. The purpose of this study was to evaluate the effectiveness and tolerance of this drug in non-allergic GINA step V asthma patients. This study was single-centre, prospective, open-label, observational, naturalistic. Non-allergic asthma patients requiring a mean dose of oral prednisolone of at least 5 mg/day during greater than or equal to 1 year or an accumulated oral corticosteroid dose/year greater than or equal to 1500 mg were enrolled. At entry and the end of the 12-month follow-up we measured blood eosinophilia and IgE concentration; at every monthly visit a forced spirometry and exhaled fraction of nitric oxide (NO) were carried out. The subjects were seven adult patients (5 female), age range 37-63 years, with the following mean values: IgE: 226.7+/-176 IU/mL; FVC 74+/-18 percent; FEV1 57+/-11 percent; NO: 21.2+/-7 ppb. The study was approved by the IRB of the hospital. One patient decided to stop treatment after 12 weeks and was excluded from the evaluation. We did not observe changes in eosinophil count, spirometry or NO values. Three patients considered responders did not need prednisolone during the follow-up. The mean daily dose of prednisolone fell from 6.6+/-8.1 mg/day at entry to 1.5+/-2.3 mg/day (p less than 0.16) at the end of follow-up. The mean monthly accumulated dose fell from 92+/-112 to 12+/-26 mg/month (p=0.26). Total blood IgE increased 1.93-fold. Side effects were only local: treatment tolerance was excellent; three out of six patients seemed to slightly benefit from anti-IgE treatment; to date there is no evidence strong enough to systematically prescribe omalizumab in non-allergic asthma patients.

摘要

奥马珠单抗是一种治疗过敏性哮喘的有效药物。本研究旨在评估该药在非过敏性 GINA 步骤 V 哮喘患者中的疗效和耐受性。这是一项单中心、前瞻性、开放性、观察性、自然史研究。纳入了需要平均每日口服泼尼松剂量至少 5mg/天大于或等于 1 年或累计口服皮质类固醇剂量/年大于或等于 1500mg 的非过敏性哮喘患者。在入组时和 12 个月随访结束时,我们测量了血嗜酸性粒细胞和 IgE 浓度;在每个月的就诊时进行了强制肺活量和呼出气一氧化氮(NO)分数的检测。受试者为 7 名成年患者(5 名女性),年龄 37-63 岁,平均数值为:IgE:226.7+/-176IU/mL;FVC 74+/-18%;FEV1 57+/-11%;NO:21.2+/-7ppb。该研究得到了医院 IRB 的批准。1 名患者在 12 周后决定停止治疗并被排除在评估之外。我们没有观察到嗜酸性粒细胞计数、肺活量或 NO 值的变化。3 名被认为是应答者的患者在随访期间不需要泼尼松。泼尼松的日平均剂量从入组时的 6.6+/-8.1mg/天降至随访结束时的 1.5+/-2.3mg/天(p<0.16)。每月累计剂量从 92+/-112mg 降至 12+/-26mg/月(p=0.26)。总血 IgE 增加了 1.93 倍。副作用仅为局部:治疗耐受性极好;6 名患者中有 3 名似乎从抗 IgE 治疗中略有获益;迄今为止,没有足够强的证据可以系统地在非过敏性哮喘患者中开具奥马珠单抗处方。

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