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贝那鲁肽治疗 6 个月的真实体验。

Real-life experience with benralizumab during 6 months.

机构信息

Pneumology Unit, 4th floor. Agencia Sanitaria Costa del Sol. Carretera Nacional 340, Km 187, 29603, Marbella, Málaga, Spain.

Yeshiva University, New York, USA.

出版信息

BMC Pulm Med. 2020 Jun 29;20(1):184. doi: 10.1186/s12890-020-01220-9.

Abstract

BACKGROUND

Benralizumab is a monoclonal antibody that binds to the human interleukin-5 (IL-5) receptor (IL-5R), thereby preventing IL-5 from binding to its receptor and inhibiting differentiation and maturation of eosinophils in the bone marrow. Because of its recent marketing approval, sufficient real-life evidence is lacking to confirm the efficacy and safety data from clinical trials. The purpose of this study was to evaluate the efficacy and safety of benralizumab for the treatment of severe refractory eosinophilic asthma in a real-world cohort of patients.

METHODS

This was a cross-sectional multicentre study of consecutive patients with severe refractory eosinophilic asthma who received treatment with benralizumab during at least 6 months. Patient follow-up was performed in specialised severe asthma units.

RESULTS

A total of 42 patients were enrolled and treated with benralizumab. Asthma control, as measured by the asthma control test (ACT), improved in all patients both at 3 months of treatment compared with baseline (13.9 ± 4 vs 20.1 ± 3.7, p < 0.001) and at 6 months of treatment compared with the results obtained at 3 months (20.1 ± 3.7 vs 21 ± 2.7, p = 0.037). Similarly, the number of emergency department visits decreased both at 3 months compared with baseline (1 [IR:0.7] vs 0 [IR:0.75], p < 0.001) and at 6 months compared with the results at 3 months (0 [IR:0.75] vs 0 [IR:0], p = 0.012). Reductions in the number of oral corticosteroid cycles, percentage of corticosteroid-dependent patients, and mean daily dose of oral or inhaled corticosteroid were also evidenced. Finally, mean lung function improvement was 291 mL (p < 0.001), and FEV1% improved both at 3 months compared with baseline (64.4 ± 9.3 vs 73.1 ± 9.1, p < 0.001) and at 6 months compared to 3 months (73.1 ± 9.1 vs 76.1 ± 12, p = 0.002). Side effects were mild and did not lead to treatment discontinuation.

CONCLUSIONS

This study confirms the efficacy and safety of benralizumab in a real-life setting with improved asthma control and lung function, and a reduced oral and inhaled corticosteroid use as well as fewer emergency department visits. In addition to a rapid initial improvement, it appears that patients continue to improve during the first 6 months of treatment.

摘要

背景

贝那鲁肽是一种单克隆抗体,可与人类白细胞介素-5(IL-5)受体(IL-5R)结合,从而阻止 IL-5 与其受体结合,并抑制骨髓中嗜酸性粒细胞的分化和成熟。由于其最近获得批准上市,因此缺乏足够的真实世界证据来证实临床试验中的疗效和安全性数据。本研究的目的是评估贝那鲁肽在真实世界的重度难治性嗜酸性粒细胞性哮喘患者队列中的疗效和安全性。

方法

这是一项多中心、横断面研究,连续纳入了至少接受贝那鲁肽治疗 6 个月的重度难治性嗜酸性粒细胞性哮喘患者。在专门的重度哮喘中心对患者进行随访。

结果

共纳入 42 例患者接受贝那鲁肽治疗。与基线相比,所有患者的哮喘控制均得到改善,采用哮喘控制测试(ACT)评估,在治疗 3 个月时(13.9±4 分比 20.1±3.7 分,p<0.001)和治疗 6 个月时(20.1±3.7 分比 3 个月时,21±2.7 分,p=0.037)均得到改善。同样,与基线相比,3 个月时急诊就诊次数减少(1 [IR:0.7] 次比 0 [IR:0.75] 次,p<0.001),与 3 个月时相比,6 个月时急诊就诊次数减少(0 [IR:0.75] 次比 0 [IR:0] 次,p=0.012)。还观察到口服皮质类固醇周期、依赖皮质类固醇患者的比例和口服或吸入皮质类固醇的平均日剂量减少。最后,平均肺功能改善 291 mL(p<0.001),与基线相比,治疗 3 个月时(64.4±9.3 分比 73.1±9.1 分,p<0.001)和治疗 6 个月时(73.1±9.1 分比 76.1±12 分,p=0.002)FEV1%均得到改善。不良反应轻微,未导致治疗中断。

结论

本研究在真实环境中证实了贝那鲁肽的疗效和安全性,可改善哮喘控制和肺功能,减少口服和吸入皮质类固醇的使用,并减少急诊就诊次数。除了初始快速改善外,患者在治疗的前 6 个月似乎仍在持续改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a16/7325276/45e261585a96/12890_2020_1220_Fig1_HTML.jpg

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