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A comparison of the effectiveness of biologic therapies for asthma: A systematic review and network meta-analysis

机译:哮喘生物疗法有效性的比较:系统评价和网状荟萃分析

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? 2022 American College of Allergy, Asthma ImmunologyBackground: Trials have not directly compared biologics for the treatment of asthma. Objective: To compare the relative efficacy of biologics in asthma. Methods: We searched MEDLINE, EMBASE, CENTRAL, and clinicaltrials.gov from inception to May 31, 2022 for randomized trials addressing biologic therapies for asthma. Reviewers worked independently and in duplicate to screen references, extract data, and assess risk of bias. We performed a frequentist network meta-analysis and assessed the certainty of evidence using the Grading of Recommendations, Assessment, Development, and Evaluations approach. We present dichotomous outcomes as absolute risk differences per 1000 patients and relative risk with 95 confidence intervals (95 CI) and continuous outcomes as mean difference (MD) and 95 CI. Results: We identified 64 trials, including 26,630 patients. For patients with eosinophilic asthma, tezepelumab (329 fewer exacerbations per 1000 95 CI, 272.6-366.6 fewer) and dupilumab (319.6 fewer exacerbations per 1000 95 CI, 272.6-357.2 fewer) reduce exacerbations compared with placebo (high certainty). Tezepelumab (MD, 0.24 L 95 CI, 0.16-0.32) and dupilumab (0.25 L 95 CI, 0.21-0.29) improve lung function compared with placebo (high certainty). Both tezepelumab (110.97 fewer hospital admissions per 1000 95 CI, 94.53-120.56 fewer) and dupilumab (97.27 fewer hospitalizations 4.11-124.67 fewer) probably reduce hospital admissions compared with placebo (moderate certainty). For patients with low eosinophils, biologics probably do not improve asthma outcomes. For these patients, tezepelumab (MD, 0.1 L 95 CI, 0-0.19) and dupilumab (MD, 0.1 L 95 CI, 0-0.20) may improve lung function (low certainty). Conclusion: Tezepelumab and dupilumab are effective at reducing exacerbations. For patients with low eosinophils, however, clinicians should probably be more judicious in using biologics, including tezepelumab, because they probably do not confer substantial benefit.
机译:?2022 年美国过敏、哮喘和免疫学会背景:试验尚未直接比较治疗哮喘的生物制剂。目的:比较生物制剂治疗哮喘的相对疗效。方法:我们检索了从建库到2022年5月31日的MEDLINE、EMBASE、CENTRAL和 clinicaltrials.gov,以寻找关于哮喘生物疗法的随机试验。评价员独立工作,重复工作,以筛选参考文献、提取资料和评估偏倚风险。我们进行了频繁的网络meta分析,并使用推荐、评估、发展和评价方法评估证据质量。我们将二分类结局表示为每1000名患者的绝对风险差和相对风险(95%置信区间(95% CI),连续结局表示为平均差(MD)和95%CI。结果:我们纳入了64项试验,包括26630名患者。对于嗜酸性粒细胞性哮喘患者,与安慰剂相比,tezepelumab(每1000例急性发作减少329例[95%CI,减少272.6-366.6例])和度普利尤单抗(每1000例减少319.6例[95%CI,减少272.6-357.2例])可减少急性发作(高质量证据)。与安慰剂相比,Tezepelumab(MD,0.24 L [95% CI,0.16-0.32])和度普利尤单抗(0.25 L [95% CI,0.21-0.29])改善肺功能(高质量证据)。tezepelumab(每1000人减少110.97例住院[95%CI,减少94.53-120.56])和度普利尤单抗(减少97.27例住院[4.11-124。与安慰剂相比,67例更少])可能会减少住院率(中等质量证据)。对于嗜酸性粒细胞低的患者,生物制剂可能不会改善哮喘的结局。对于这些患者,tezepelumab(MD,0.1 L [95% CI,0-0.19])和度普利尤单抗(MD,0.1 L [95% CI,0-0.20])可以改善肺功能(低质量证据)。结论:替司柳单抗和度普利尤单抗可有效减少急性加重。然而,对于嗜酸性粒细胞低的患者,临床医生在使用生物制剂(包括 tezepelumab)时可能应该更明智,因为它们可能不会带来实质性的益处。

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