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GATA3 特异性 DNA 酶可减轻嗜酸性 COPD 患者痰中嗜酸性粒细胞增多:一项可行性随机临床试验。

A GATA3-specific DNAzyme attenuates sputum eosinophilia in eosinophilic COPD patients: a feasibility randomized clinical trial.

机构信息

Department of Medicine, Pulmonary and Critical Care Medicine, University Medical Centre Giessen and Marburg, Philipps-University, Member of the German Centre for Lung Research (DZL), Marburg, Germany.

Department of Respiratory Medicine, Hannover Medical School, Fraunhofer Institute for Toxicology and Experimental Medicine, Member of the German Centre for Lung Research (DZL), Hannover, Germany.

出版信息

Respir Res. 2018 Apr 4;19(1):55. doi: 10.1186/s12931-018-0751-x.

Abstract

BACKGROUND

A subset of COPD-patients presents with eosinophilic airway inflammation. While treatment of asthmatic patients with the GATA3-specific DNAzyme SB010 attenuated sputum eosinophilia after allergen challenge, this specific treatment has not been evaluated in patients with COPD. Our objective was to evaluate the feasibility and safety of inhaled SB010 in COPD patients with sputum eosinophilia.

METHODS

We conducted a randomized, double-blind, placebo-controlled, multicentre clinical trial in COPD-patients with sputum eosinophilia (≥2.5% non-squamous cells). Patients inhaled 10 mg SB010 bid or matching placebo via the controlled inhalation system AKITA2 APIXNEB for 28 days. Endpoints included the feasibility of the study (primary), patient's safety, sputum eosinophils, FNO, lung function, symptoms, and biomarkers. The study was registered in the German Clinical Trials Register: DRKS00006087.

RESULTS

One hundred thirty patients were screened, 23 patients were randomized (FEV 49.4 ± 11.5%; sputum eosinophils 8.0 ± 8.4%) and 19 patients completed the study (10 placebo, 9 SB010. After 28 days, SB010 decreased the relative sputum eosinophil count (p = 0.004) as compared to no changes in placebo-treated patients. FNO, lung function, and symptoms were not affected significantly. We found an increase in blood IFN-γ (p = 0.02) and a trend to lower IL-5 levels in patients treated with SB010. SB010 was safe and well tolerated. Thirty five AEs (22 SB010, 13 placebo including 1 SAE) were observed with 3 AEs in each group judged to be possibly treatment-related.

CONCLUSION

In patients with eosinophilic COPD, sputum eosinophils could be reduced by inhalation of SB010. Long-term studies are needed to demonstrate clinical efficacy.

摘要

背景

一部分 COPD 患者表现出嗜酸性气道炎症。虽然用 GATA3 特异性 DNA 酶 SB010 治疗哮喘患者可减轻过敏原激发后痰中嗜酸性粒细胞增多,但尚未在 COPD 患者中评估这种特异性治疗。我们的目的是评估吸入 SB010 在 COPD 患者中痰嗜酸性粒细胞增多的可行性和安全性。

方法

我们进行了一项随机、双盲、安慰剂对照、多中心临床试验,纳入了痰嗜酸性粒细胞增多(≥2.5%非鳞状细胞)的 COPD 患者。患者通过 AKITA2 APIXNEB 控制吸入系统每天吸入 10mg SB010 两次或匹配的安慰剂,共 28 天。主要终点包括研究的可行性(首要终点)、患者安全性、痰嗜酸性粒细胞、FENO、肺功能、症状和生物标志物。该研究在德国临床试验注册中心(DRKS00006087)进行了注册。

结果

共筛选了 130 名患者,23 名患者被随机分组(FEV1 为 49.4±11.5%;痰嗜酸性粒细胞为 8.0±8.4%),19 名患者完成了研究(10 名安慰剂,9 名 SB010)。28 天后,SB010 降低了相对痰嗜酸性粒细胞计数(p=0.004),而安慰剂组患者无变化。FENO、肺功能和症状无明显变化。我们发现,与安慰剂相比,SB010 治疗患者的血液 IFN-γ水平升高(p=0.02),IL-5 水平呈下降趋势。SB010 安全且耐受良好。共观察到 35 例不良事件(22 例 SB010,13 例安慰剂,包括 1 例严重不良事件),其中每组各有 3 例不良事件被判断为可能与治疗相关。

结论

在嗜酸性 COPD 患者中,SB010 吸入可降低痰嗜酸性粒细胞。需要进行长期研究以证明临床疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d491/5883532/622b7fa74ec9/12931_2018_751_Fig1_HTML.jpg

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