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患者接受 benralizumab 治疗长达 5 年的安全性和疗效综合评估。

Integrated Safety and Efficacy Among Patients Receiving Benralizumab for Up to 5 Years.

机构信息

Thoraxklinik Heidelberg and IKF Pneumologie, Heidelberg and Mainz, Germany.

PhyMedExp, Université de Montpellier, INSERM, CNRS, Département de Pneumologie et Addictologie, CHU de Montpellier, Montpellier, France.

出版信息

J Allergy Clin Immunol Pract. 2021 Dec;9(12):4381-4392.e4. doi: 10.1016/j.jaip.2021.07.058. Epub 2021 Sep 4.

Abstract

BACKGROUND

Benralizumab is an IL-5Rα-directed monoclonal antibody indicated for patients with severe, uncontrolled eosinophilic asthma.

OBJECTIVE

To evaluate the long-term safety and tolerability of benralizumab among adults treated for up to 5 years.

METHODS

This analysis included adults treated with placebo or subcutaneous benralizumab 30 mg every 4 or 8 weeks in the 48-week SIROCCO, 56-week CALIMA, and 28-week ZONDA pivotal trials, who were subsequently enrolled in the 56-week double-blind BORA extension and continued assigned regimens or initiated benralizumab (if previously on placebo) for 16 to 40 weeks, before entering the open-label MELTEMI extension. Safety was measured by adverse and serious adverse event rates. Exacerbations were evaluated in patients with blood eosinophils greater than or equal to 300 cells/μL receiving high-dose inhaled corticosteroids at baseline.

RESULTS

Overall, 446 received treatment and 384 (86.1%) completed the study; 157 (35.2%) received benralizumab for 4 or more years. Adverse and serious adverse event rates (28.5-32.4 and 6.3-8.4 per 100 patient-years, respectively) were low, stable over time, and did not increase with exposure; few (n = 8) discontinued because of adverse events. Serious infections and hypersensitivity event rates were consistent with those in previous studies. Among patients with blood eosinophils greater than or equal to 300 cells/μL-high-dosage inhaled corticosteroids receiving benralizumab every 8 weeks, at least 75% had zero exacerbations annually during the integrated analysis period.

CONCLUSIONS

In patients with severe, uncontrolled eosinophilic asthma, long-term benralizumab was safe and well tolerated for up to 5 years. There were no new safety signals, and exacerbations were eliminated in similar percentages of patients as in predecessor studies.

摘要

背景

本那鲁单抗是一种靶向 IL-5Rα 的单克隆抗体,适用于治疗严重、未得到控制的嗜酸性粒细胞性哮喘患者。

目的

评估本那鲁单抗在长达 5 年的治疗期间成人患者中的长期安全性和耐受性。

方法

本分析纳入了在 48 周 SIROCCO、56 周 CALIMA 和 28 周 ZONDA 关键性试验中接受安慰剂或皮下注射本那鲁单抗 30mg、每 4 或 8 周一次治疗的成人患者,随后入组了 56 周双盲 BORA 扩展期,并继续接受之前的方案治疗或接受本那鲁单抗(如果之前接受安慰剂治疗)治疗 16 至 40 周,之后进入开放标签 MELTEMI 扩展期。通过不良反应和严重不良反应发生率来评估安全性。在基线时接受高剂量吸入性皮质类固醇治疗且血液嗜酸性粒细胞计数大于或等于 300 个/μL 的患者中评估加重事件。

结果

共有 446 例患者接受了治疗,384 例(86.1%)完成了研究;157 例(35.2%)接受本那鲁单抗治疗超过 4 年。不良反应和严重不良反应发生率(分别为 28.5-32.4 和 6.3-8.4/100 患者-年)较低,随时间保持稳定,且未随暴露增加而增加;少数(n=8)患者因不良反应而停药。严重感染和过敏事件发生率与之前的研究一致。在基线时接受高剂量吸入性皮质类固醇治疗且血液嗜酸性粒细胞计数大于或等于 300 个/μL 的患者中,接受本那鲁单抗每 8 周一次治疗的患者,在整合分析期间至少有 75%的患者每年的加重次数为 0。

结论

在严重、未得到控制的嗜酸性粒细胞性哮喘患者中,本那鲁单抗长期治疗长达 5 年是安全且耐受良好的。未出现新的安全性信号,且在类似比例的患者中消除了加重。

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