Harvard T.H. Chan School of Public Health, Boston, Mass; Chung Shan Medical University, Taichung, Taiwan.
Division of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Mass; Chulalongkorn University, Bangkok, Thailand.
J Allergy Clin Immunol Pract. 2023 May;11(5):1475-1484.e20. doi: 10.1016/j.jaip.2022.12.046. Epub 2023 Jan 28.
Antidrug antibodies (ADAs) may worsen the efficacy and safety of biologics. However, little is known about the incidence of ADAs associated with the 6 biologics approved for the treatment of asthma in the United States.
To elucidate the incidence of ADAs and their impact on reported clinical outcomes.
Systematic review and meta-analyses of randomized controlled trials, open-label extension studies, and nonrandomized studies of biologics in patients with asthma indexed in PubMed, Embase, and CENTRAL between January 1, 2000, and July 9, 2022, were carried out. The primary outcomes were treatment-emergent ADAs (incidence) and ADA prevalence.
A total of 46 studies met the eligibility criteria. ADA incidence over follow-up was 2.91% (95% CI, 1.60-4.55) and was highest in the benralizumab studies (8.35%), with a risk ratio of 4.9 (2.69-8.92) when compared with placebo, and lowest in the omalizumab studies (0.00%). Incidence was 7.61% in the dupilumab studies, 4.39% in reslizumab, 3.63% in mepolizumab, and 1.12% in the tezepelumab studies. Incidence of neutralizing antibodies was 0.00% to 10.74% and was highest for benralizumab (7.12%). Incidence of neutralizing antibodies was higher in the benralizumab every 8 weeks (8.17%) versus every 4 weeks arms (5.81%). Results were consistent in subgroup analyses by study type and length of follow-up.
Approximately 2.9% of individuals in the included studies developed ADAs over study follow-up period. The incidence was highest in the benralizumab group and lowest in the omalizumab group. The subcutaneous route and longer dosing intervals were associated with higher ADA development.
抗体药物(ADAs)可能会降低生物制剂的疗效和安全性。然而,对于美国批准用于治疗哮喘的 6 种生物制剂相关 ADA 的发生率及其对报告的临床结局的影响,人们知之甚少。
阐明 ADA 的发生率及其对报告的临床结局的影响。
对 2000 年 1 月 1 日至 2022 年 7 月 9 日期间在 PubMed、Embase 和 CENTRAL 中索引的哮喘患者的生物制剂随机对照试验、开放标签扩展研究和非随机研究进行系统评价和荟萃分析。主要结局为治疗出现的 ADA(发生率)和 ADA 患病率。
共有 46 项研究符合入选标准。随访期间 ADA 的发生率为 2.91%(95%CI,1.60-4.55),在 benralizumab 研究中最高(8.35%),与安慰剂相比风险比为 4.9(2.69-8.92),而在 omalizumab 研究中最低(0.00%)。dupilumab 研究中的发生率为 7.61%,reslizumab 为 4.39%,mepolizumab 为 3.63%,tezepelumab 为 1.12%。中和抗体的发生率为 0.00%至 10.74%,benralizumab 最高(7.12%)。benralizumab 每 8 周(8.17%)与每 4 周(5.81%)治疗组的中和抗体发生率较高。按研究类型和随访时间的亚组分析结果一致。
在纳入研究的个体中,大约有 2.9%的个体在研究随访期间出现 ADA。发生率在 benralizumab 组最高,在 omalizumab 组最低。皮下给药途径和较长的给药间隔与 ADA 的发展有关。