Department of Respiratory Medicine, Ghent University Hospital and Ghent University, Belgium.
Respir Med. 2009 Nov;103(11):1633-42. doi: 10.1016/j.rmed.2009.06.014. Epub 2009 Jul 19.
To evaluate the 16- and 52-week effectiveness of add-on omalizumab treatment under real-life heterogeneity in patients, settings, and physicians in an open-label, multicenter, pharmaco-epidemiologic study of patients with severe persistent allergic asthma in Belgium.
Effectiveness outcomes included improvement in 2005 global initiative for asthma (GINA) classification, physician-rated global evaluation of treatment effectiveness (GETE), quality of life (Juniper asthma-related quality of life (AQLQ) and European quality of life questionnaire 5 dimensions (EQ-5D)), and severe asthma exacerbations. Patients studied included both intent-to-treat and per-protocol populations.
The sample (n=158) had a mean age of 48.17+/-17.18 years, and a slight majority were female (53.8%). Despite being treated with high-dose inhaled corticosteroids and long-acting beta2-agonists, all patients experienced frequent symptoms and had exacerbations in the past year. At 16 weeks, >82% had good/excellent GETE (P values <0.001), >82% had an improvement in total AQLQ scores of > or =0.5 points (P<0.001), and >91% were severe exacerbation-free (P<0.001). At 52 weeks, >72% had a good/excellent GETE rating (P<0.001), >84% had improvements in total AQLQ score of > or =0.5 points (P<0.001), >56% had minimally important improvements in EQ-5D utility scores (P=0.012), and >65% were severe exacerbation-free (P<0.001). Significant reductions in healthcare utilization compared to the one year prior to treatment were noted.
The PERSIST study shows better physician-rated effectiveness, greater improvements in quality of life, greater reductions in exacerbation rates, and greater reductions in healthcare utilization than previously reported in efficacy studies. Under real-life conditions, omalizumab is effective as add-on therapy in the treatment of patients with persistent severe allergic asthma.
在比利时的一项开放性、多中心、药物流行病学研究中,评估奥马珠单抗附加治疗在患者、环境和医生的真实世界异质性下,在重度持续性过敏性哮喘患者中的 16 周和 52 周疗效。
疗效结局包括 2005 年全球哮喘倡议(GINA)分类、医生评价的治疗效果总体评估(GETE)、生活质量(Juniper 哮喘相关生活质量(AQLQ)和欧洲生活质量问卷 5 维度(EQ-5D))和重度哮喘恶化的改善。研究对象包括意向治疗和方案人群。
该样本(n=158)的平均年龄为 48.17±17.18 岁,略多数为女性(53.8%)。尽管接受了高剂量吸入皮质激素和长效β2-激动剂治疗,但所有患者都有频繁的症状,且在过去一年中都有恶化。在 16 周时,>82%的患者 GETE 良好/优秀(P 值<0.001),>82%的患者总 AQLQ 评分改善≥0.5 分(P<0.001),>91%的患者无重度恶化(P<0.001)。在 52 周时,>72%的患者 GETE 评分良好/优秀(P<0.001),>84%的患者总 AQLQ 评分改善≥0.5 分(P<0.001),>56%的患者 EQ-5D 效用评分有微小但重要的改善(P=0.012),>65%的患者无重度恶化(P<0.001)。与治疗前一年相比,医疗保健利用率显著降低。
PERSIST 研究显示,与以前的疗效研究相比,奥马珠单抗附加治疗在重度持续性过敏性哮喘患者中具有更好的医生评价疗效、更大的生活质量改善、更大的恶化率降低和更大的医疗保健利用率降低。在真实环境下,奥马珠单抗作为附加疗法治疗持续性重度过敏性哮喘是有效的。