P202 Real life experience with mepolizumab and comparison with omalizumab in children with severe asthma

J. Ko, A. Jamalzadeh, S. Makhecha, S. Saglani, A. Bush, L. Fleming
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引用次数: 0

Abstract

the one type-2 biomarker frequency-weighted in and respectively. contrast, the 814 patients with both biomarkers low at baseline had observed vs predicted rate ratios of 0.86 vs 1.00; the corresponding percentages reduction in asthma attacks were 14% and 0%, respectively. The relative risk associated with biomarkers was consistent across populations, but the absolute risk and the treatment benefit conferred by type-2 biomarkers was greater in a population at higher background risk. The prototype ORACLE scale predicts the excess risk conferred by raised biomarkers which is removed by anti-inflammatory therapy in trial populations. for large-scale paediatric mepolizumab studies, especially given evidence of low Type-2 cytokines in children with severe asthma.
P202 mepolizumab与omalizumab治疗严重哮喘儿童的比较
1个2型生物标志物频率加权分别为和。相比之下,814名两种生物标志物在基线时均较低的患者的观察率与预测率之比为0.86比1.00;相应的哮喘发作减少百分比分别为14%和0%。与生物标志物相关的相对风险在人群中是一致的,但在背景风险较高的人群中,2型生物标志物的绝对风险和治疗益处更大。原型ORACLE量表预测了在试验人群中通过抗炎治疗消除的升高的生物标志物所带来的超额风险。用于大规模的儿科美polizumab研究,特别是在重度哮喘儿童中存在低2型细胞因子的证据。
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