Real-life efficacy and safety of omalizumab in Portuguese patients with persistent uncontrolled asthma

被引:8
|
作者
Pereira Barbosa, M. [1 ]
Bugalho de Almeida, A. [2 ]
Pereira, C. [3 ]
Chen, C. -W. [4 ]
Georgiou, P. [5 ]
Peachey, G. [5 ]
机构
[1] Ctr Hosp Lisboa Norte, Serv Imunoalergol, Lisbon, Portugal
[2] Univ Lisbon, Fac Med, Clin Univ Pneumol, P-1699 Lisbon, Portugal
[3] Novartis Farma Prod Farmaceut SA, Ave Prof Doutor Cavaco Silva 10E,Taguspk, P-2740255 Porto Salvo, Portugal
[4] Novartis Pharmaceut, E Hanover, NJ 07936 USA
[5] Novartis Pharmaceut UK Ltd, Horsham RH12 5AB, W Sussex, England
关键词
Omalizumab; Allergic asthma; Anti-immunoglobulin E; Asthma control; Exacerbations; Observational study; ALLERGIC-ASTHMA; EXPERIENCE; BURDEN;
D O I
10.1016/j.rppnen.2014.07.004
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Introduction: The real life effectiveness, safety and the use of omalizumab for Portuguese patients with uncontrolled persistent allergic asthma are not sufficiently well known. The objective of this report was to make an evaluation, in a post-marketing, non-interventional, observational registry, of the Portuguese population included in the eXpeRience study. Methods: The methods used in this report are the same as the global eXpeRience ones, applied to a Portuguese sub-population. Patients with uncontrolled allergic asthma who had started omalizumab within the previous 15 weeks were enrolled and received omalizumab add-on therapy for 24 months. The physicians' global evaluation of treatment effectiveness (GETE), asthma symptoms and control (ACT score), quality of life (mini-AQLQ score), exacerbations, and serious adverse events (SAE) were reported. Results: Of the 943 patients recruited in the eXpeRience registry, 62 patients were from Portugal. 62.1% of them were observed to be responders with good/excellent GETE assessment at Week 16. Clinically meaningful improvements in asthma control (ACT score) and quality of life (mini-AQLQ score) were observed with omalizumab therapy at Months 12 (mean change: +7.7 [n = 35]; +2.1 [n = 20], respectively) and 24 (mean change: +7.0 [n = 26]; +2.7 [n = 13], respectively). Asthma symptoms and rescue medication usage were reduced to = 1 day/week at Month 24 from a baseline of = 3.5 days/week. The proportion of patients with no clinically significant exacerbations increased from 6.5% during pre-treatment (n = 62) to 50% at Month 12 (n = 54) and 60% at Month 24 (n = 45). Conclusion: The findings from the Portugal subpopulation of eXpeRience registry confirm that omalizumab add-on therapy is efficacious and well tolerated in the management of uncontrolled persistent allergic asthma. Another pertinent issue is the fact that the Portuguese subpopulation response is similar to the international population average of the study. (C) 2014 Sociedade Portuguesa de Pneumologia. Published by Elsevier Espana, S.L.U. All rights reserved.
引用
收藏
页码:151 / 156
页数:6
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