Possible Protective Effect of Omalizumab on Lung Function Decline in Patients Experiencing Asthma Exacerbations

被引:13
作者
Busse, William W. [1 ]
Szefler, Stanley J. [2 ,3 ]
Haselkorn, Tmirah [4 ]
Iqbal, Ahmar [5 ]
Ortiz, Benjamin [6 ]
Lanier, Bobby Q. [7 ]
Chipps, Bradley E. [8 ]
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Madison, WI 53792 USA
[2] Childrens Hosp Colorado, Aurora, CO USA
[3] Univ Colorado, Sch Med, Aurora, CO USA
[4] EpiMetrix Inc, Los Altos, CA USA
[5] Genentech Inc, San Francisco, CA 94080 USA
[6] Novartis Pharmaceut, E Hanover, NJ USA
[7] Univ North Texas, Hlth Sci Ctr, Ft Worth, TX USA
[8] Capital Allergy & Resp Dis Ctr, Sacramento, CA USA
关键词
Asthma; Lung function; Airway remodeling; Inflammation; Lung function decline; Obstructive airway disease; FUTURE EXACERBATION; CHILDHOOD; INFLAMMATION; FREQUENCY; THERAPY; RISK;
D O I
10.1016/j.jaip.2020.10.027
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
BACKGROUND: Frequent exacerbations are associated with greater FEV1 decline in patients with asthma. The effect of omalizumab versus placebo on lung function in patients experiencing asthma exacerbations has not been previously examined. OBJECTIVE: To evaluate the relationship between post-baseline (treatment phase) exacerbation status and lung function decline in children, adolescents, and adults treated with omalizumab versus placebo using data from 3 pediatric and adolescent/adult studies. METHODS: Changes in percent predicted FEV1 (ppFEV(1)) and FEV1 by treatment (omalizumab/placebo) and postbaseline exacerbation status (exacerbators/nonexacerbators) were assessed in patients aged 6 to 11 years (IA05, n = 576) and 12 to 75 years (EXTRA/INNOVATE pooled, n = 1202). Pediatric patients were examined at treatment weeks 12, 24, 28, 40, and 52, and adolescent/adult data at weeks 4, 12, 20, and 28. RESULTS: Omalizumab-treated patients experienced larger increases in ppFEV(1) and FEV1 compared with placebo-treated patients in the pediatric and pooled adolescent/adult populations. The response was observed in pediatric exacerbators, with significantly larger increases in ppFEV(1) and FEV1 at week 12 (mean difference [95% CI], 4.11% [0.93%-7.30%], P = .011 for ppFEV(1); 80 [10-140] mL, P = .017 for FEV1) and week 28 (mean difference [95% CI], 3.65% [0.11%-7.19%], P = .043 for ppFEV(1); 100 [30-170] mL, P = .007 for FEV1). In the adolescent/adult population, both exacerbators and nonexacerbators derived similar benefit with omalizumab compared with placebo. CONCLUSIONS: Findings from this post hoc analysis suggest that omalizumab may confer some protection against lung function decline among patients who experienced exacerbations during treatment. (C) 2020 Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology
引用
收藏
页码:1201 / 1211
页数:11
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