Koppitz Martin, Eschenburg Charlotte, Salzmann Emilia, Rosewich Martin, Schubert Ralf, Zielen Stefan
Department for Children and Adolescents, Division for Allergology, Pneumology and Cystic Fibrosis, University Hospital Goethe University, Frankfurt am Main, Germany.
Department for Children and Adolescents, Division for Stem Cell Transplantation and Immunology, University Hospital Goethe University, Frankfurt am Main, Germany.
PLoS One. 2016 Jun 16;11(6):e0156999. doi: 10.1371/journal.pone.0156999. eCollection 2016.
Mucoactive drugs should increase the ability to expectorate sputum and, ideally, have anti-inflammatory properties. The aim of the study was to evaluate the mucolytic activity of Tyloxapol compared to saline (0.9%) in COPD.
A randomized, placebo-controlled, double-blinded crossover, clinical trial was carried out. Patients were randomly assigned to either inhale 5 ml Tyloxapol 1% or saline 0.9% solution three times daily for 3 weeks and vice versa for another 3 weeks. 28 patients (18 male, 10 female, 47 to 73 years old, median age 63.50) were screened, 21 were treated and 19 patients completed the study per protocol.
A comparison of the two treatment phases showed that the primary endpoint sputum weight was statistically significant higher when patients inhaled Tyloxapol (mean 4.03 g, 95% CI: 2.34-5.73 g at week 3) compared to saline (mean 2.63 g, 95% CI: 1.73-3.53 g at week 3). The p-value at three weeks of treatment was 0.041 between treatment arms. Sputum cells decreased during the Tyloxapol treatment after 3 weeks, indicating that Tyloxapol might have some anti-neutrophilic properties. Lung function parameters (FVC, FEV1, RV, and RV/TLC) remained stable during the study, and no treatment effect was shown. Interestingly, there was a mean increase in all inflammatory cytokines (IL-1β, IL-6, and IL-8) during the saline treatment from day 1 to week 3, whereas during the Tyloxapol treatment, all cytokines decreased. Due to the small sample size and the large individual variation in sputum cytokines, these differences were not significant. However, analyses confirmed that Tyloxapol has significant anti-inflammatory properties in vitro. Despite the high number of inhalations (more than 1000), only 27 adverse events (20 during the Tyloxapol and seven during saline) were recorded. Eleven patients experienced AEs under Tyloxapol and six under saline treatment, which indicates that inhalation of saline or Tyloxapol is a very safe procedure.
Our study demonstrated that inhalation of Tyloxapol by patients with COPD is safe and superior to saline and has some anti-inflammatory effects.
ClinicalTrials.gov NCT02515799.
黏液活性药物应提高痰液咳出能力,理想情况下还应具有抗炎特性。本研究旨在评估泰洛沙泊与生理盐水(0.9%)相比在慢性阻塞性肺疾病(COPD)中的黏液溶解活性。
进行了一项随机、安慰剂对照、双盲交叉临床试验。患者被随机分配,每日三次吸入5毫升1%的泰洛沙泊溶液或0.9%的生理盐水溶液,为期3周,然后交换治疗3周。共筛选了28例患者(18例男性,10例女性,年龄47至73岁,中位年龄63.50岁),21例接受治疗,19例按方案完成研究。
两个治疗阶段的比较显示,与生理盐水(第3周时平均2.63克,95%置信区间:1.73 - 3.53克)相比,患者吸入泰洛沙泊时主要终点指标痰液重量在统计学上显著更高(第3周时平均4.03克,95%置信区间:2.34 - 5.73克)。治疗3周时治疗组间的p值为0.041。泰洛沙泊治疗3周后痰液细胞减少,表明泰洛沙泊可能具有一些抗中性粒细胞特性。研究期间肺功能参数(用力肺活量(FVC)、第1秒用力呼气容积(FEV1)、残气量(RV)和残气量/肺总量(RV/TLC))保持稳定,未显示出治疗效果。有趣的是,从第1天到第3周的生理盐水治疗期间,所有炎症细胞因子(白细胞介素 - 1β(IL - 1β)、白细胞介素 - 6(IL - 6)和白细胞介素 - 8(IL - 8))均有平均升高,而在泰洛沙泊治疗期间,所有细胞因子均下降。由于样本量小且痰液细胞因子个体差异大,这些差异不显著。然而,分析证实泰洛沙泊在体外具有显著的抗炎特性。尽管吸入次数众多(超过1000次),仅记录到27例不良事件(泰洛沙泊治疗期间20例,生理盐水治疗期间7例)。11例患者在泰洛沙泊治疗下出现不良事件,6例在生理盐水治疗下出现不良事件,这表明吸入生理盐水或泰洛沙泊是非常安全的操作。
我们的研究表明,COPD患者吸入泰洛沙泊是安全的,优于生理盐水,且具有一定的抗炎作用。
ClinicalTrials.gov NCT02515799