Suppr超能文献

奥马珠单抗治疗重度过敏性哮喘的真实世界疗效:一项观察性研究的荟萃分析。

Real-World Effectiveness of Omalizumab in Severe Allergic Asthma: A Meta-Analysis of Observational Studies.

机构信息

Contre les Maladies Chroniques pour un VIeillissement Actif (MACVIA) en France European Innovation Partnership on Active and Healthy Ageing Reference Site, Montpellier, France; Centre Hospitalier Universitaire de Montpellier, Montpellier, France; Charité, Universitätsmedizin Berlin, Humboldt-Universität zu Berlin, Berlin, Germany; Department of Dermatology and Allergy, Comprehensive Allergy Center, Berlin Institute of Health, Berlin, Germany.

School of Medicine, Université Paris-Saclay, Le Kremlin-Bicêtre, France; INSERM UMR_S 999, Hôpital Marie Lannelongue, Le Plessis-Robinson, France; AP-HP, Department of Respiratory and Intensive Care Medicine, Hôpital Bicêtre, Le Kremlin-Bicêtre, France.

出版信息

J Allergy Clin Immunol Pract. 2021 Jul;9(7):2702-2714. doi: 10.1016/j.jaip.2021.01.011. Epub 2021 Jan 21.

Abstract

BACKGROUND

Assessment of clinical outcomes in the real-world corroborates findings from randomized controlled trials (RCTs).

OBJECTIVE

This meta-analysis evaluated real-world data of omalizumab on treatment response, lung function, exacerbations, oral corticosteroid (OCS) use, patient-reported outcomes (PROs), health care resource utilization (HCRU), and school/work absenteeism at 4, 6, and 12 months after treatment.

METHODS

Observational studies in patients with severe allergic asthma (≥6 years) treated with omalizumab for ≥16 weeks, published from January 2005 to October 2018, were retrieved from PubMed, Embase, and Cochrane. A random-effects model was used to assess heterogeneity.

RESULTS

In total, 86 publications were included. Global evaluation of treatment effectiveness (GETE) was good/excellent in 77% patients at 16 weeks (risk difference: 0.77; 95% confidence interval [CI]: 0.70-0.84; I = 96%) and in 82% patients at 12 months (0.82, 0.73-0.91; 97%). The mean improvement in forced expiratory volume in 1 second was 160, 220, and 250 mL at 16 weeks, 6 months, and 12 months, respectively. There was a decrease in Asthma Control Questionnaire score at 16 weeks (-1.14), 6 months (-1.56), and 12 months (-1.13) after omalizumab therapy. Omalizumab significantly reduced annualized rate of severe exacerbations (risk ratio [RR]: 0.41, 95% CI: 0.30-0.56; I = 96%), proportion of patients receiving OCS (RR: 0.59, 95% CI: 0.47-0.75; I = 96%), and number of unscheduled physician visits (mean difference: -2.34, 95% CI: -3.54 to -1.13; I = 98%) at 12 months versus baseline.

CONCLUSION

The consistent improvements in GETE, lung function, and PROs, and reductions in asthma exacerbations, OCS use, and HCRU with add-on omalizumab in real-life confirm and complement the efficacy data of RCTs.

摘要

背景

真实世界的临床结局评估与随机对照试验(RCT)的结果相符。

目的

本荟萃分析评估了奥马珠单抗治疗后 4、6 和 12 个月时治疗反应、肺功能、加重、口服皮质类固醇(OCS)使用、患者报告结局(PRO)、医疗资源利用(HCRU)和学校/工作缺勤的真实世界数据。

方法

从 2005 年 1 月至 2018 年 10 月,检索了发表在 PubMed、Embase 和 Cochrane 上的奥马珠单抗治疗≥16 周的重度过敏性哮喘(≥6 岁)患者的观察性研究。使用随机效应模型评估异质性。

结果

共纳入 86 篇文献。16 周时,77%的患者获得了良好/优秀的总体治疗效果评估(GETE)(风险差异:0.77;95%置信区间 [CI]:0.70-0.84;I=96%),12 个月时,82%的患者获得了良好/优秀的评估(0.82,0.73-0.91;97%)。16 周、6 个月和 12 个月时,用力呼气量(FEV1)的平均改善量分别为 160、220 和 250mL。奥马珠单抗治疗后,哮喘控制问卷评分在 16 周时下降了-1.14,在 6 个月时下降了-1.56,在 12 个月时下降了-1.13。奥马珠单抗显著降低了重度加重的年化发生率(风险比 [RR]:0.41,95%CI:0.30-0.56;I=96%)、OCS 使用率(RR:0.59,95%CI:0.47-0.75;I=96%)和未经计划的医生就诊次数(平均差异:-2.34,95%CI:-3.54 至-1.13;I=98%),12 个月时与基线相比。

结论

在真实世界中,奥马珠单抗治疗的 GTE、肺功能和 PRO 持续改善,哮喘加重、OCS 使用和 HCRU 减少,这证实并补充了 RCT 的疗效数据。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验