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Comparative efficacy of mepolizumab, benralizumab, and dupilumab in eosinophilic asthma: A Bayesian network meta-analysis
被引:46
|作者:
Akenroye, Ayobami
[1
,2
,3
,4
]
Lassiter, Grace
[5
]
Jackson, John W.
[4
,6
,7
]
Keet, Corinne
[8
]
Segal, Jodi
[4
,6
,9
]
Alexander, G. Caleb
[4
,6
,9
]
Hong, Hwanhee
[10
]
机构:
[1] Brigham & Womens Hosp, Div Allergy & Clin Immunol, 60 Fenwood Rd, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Channing Div Network Med, Boston, MA 02115 USA
[3] Harvard Med Sch, Boston, MA 02115 USA
[4] Johns Hopkins Bloomberg Sch Pub Hlth, Dept Epidemiol, Baltimore, MD USA
[5] Georgetown Coll Med, Washington, DC USA
[6] Johns Hopkins Bloomberg Sch Publ Hlth, Ctr Drug Safety & Effectiveness, Baltimore, MD USA
[7] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Mental Hlth, Baltimore, MD USA
[8] Univ N Carolina, Div Pediat Allergy & Immunol, Chapel Hill, NC 27515 USA
[9] Johns Hopkins Univ, Div Gen Internal Med, Sch Med, Baltimore, MD USA
[10] Duke Univ, Dept Biostat & Bioinformat, Durham, NC USA
基金:
美国国家卫生研究院;
关键词:
Asthma;
eosinophilic;
mepolizumab;
benralizumab;
dupilumab;
network meta-analysis;
Bayesian;
monoclonal antibody;
comparative effectiveness;
QUALITY-OF-LIFE;
DOUBLE-BLIND;
INHALED CORTICOSTEROIDS;
MULTICENTER;
RANKING;
SIROCCO;
DISEASE;
SAFETY;
DREAM;
D O I:
10.1016/j.jaci.2022.05.024
中图分类号:
R392 [医学免疫学];
学科分类号:
100102 ;
摘要:
Background: The comparative safety and efficacy of the biologics currently approved for asthma are unclear. Objective: We compared the safety and efficacy of mepolizumab, benralizumab, and dupilumab in individuals with severe eosinophilic asthma. Methods: We performed a systematic review of peer-reviewed literature published 2000 to 2021. We studied Bayesian network meta-analyses of exacerbation rates, prebronchodilator FEV1, the Asthma Control Questionnaire, and serious adverse events in individuals with eosinophilic asthma. Results: Eight randomized clinical trials (n = 6461) were identified. We found in individuals with eosinophils >= 300 cells/mu L the following: in reducing exacerbation rates compared to placebo: dupilumab (risk ratio [RR], 0.32; 95% credible interval [CI], 0.23 to 0.45), mepolizumab (RR, 0.37; 95% CI, 0.30 to 0.45), and benralizmnab (RR, 0.49; 95% CI, 0.43 to 0.55); in improving FEV1: dupilumab (mean difference in milliliters [MD] 230; 95% CI, 160 to 300), benralizumab (MD, 150; 95% CI, 100 to 200), and mepolizumab (MD, 150; 95% CI, 66 to 220); and in reducing Asthma Control Questionnaire scores: mepolizumab (MD, -0.63; 95% CI, -0.81 to -0.45), dupilumab (MD, -0.48; 95% CI, -0.83 to - 0.14), and benralizumab (MD, -0.32; 95% CI, -0.43 to - 0.21). In individuals with eosinophils 150-299 cells/mu L, benralizmnab (RR, 0.62; 95% CI, 0.52 to 0.73) and dupilumab (RR, 0.60; 95% CI, 0.38 to 0.95) were associated with lower exacerbation rates; and only benralizumab (MD, 81; 95% CI, 8 to 150) significantly improved FEV1. These differences were minimal compared to clinically important thresholds. For serious adverse events in the overall population, mepolizumab (odds ratio, 0.67; 95% CI, 0.48 to 0.92) and benralizumab (odds ratio, 0.74; 95% CI, 0.59 to 0.93) were associated with lower odds of a serious adverse event, while dupilumab was not different from placebo (odds ratio, 1.0; 95% CI, 0.74 to 1.4). Conclusion: There are minimal differences in the efficacy and safety of mepolizumab, benralizumab, and dupilumab in eosinophilic asthma.
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页码:1097 / +
页数:21
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