Effect of Carbocysteine on Exacerbations and Lung Function in Patients With Mild-to-Moderate Chronic Obstructive Pulmonary Disease: A Multicentre, Double-Blind, Randomized, Placebo-Controlled Trial
Yumin Zhou , Fan Wu , Haiqing Li , Zhishan Deng , Li Lin , Hong Huang , Haiyan Zhao , Yiran Wang , Lingwei Wang , Qijian Cheng , Shan Cai , Zhiyi He , Yinghua Ying , Peiyu Huang , Heshen Tian , Jieqi Peng , Shan Xiao , Xiang Wen , Huajing Yang , Youlan Zhen , Pixin Ran
{"title":"Effect of Carbocysteine on Exacerbations and Lung Function in Patients With Mild-to-Moderate Chronic Obstructive Pulmonary Disease: A Multicentre, Double-Blind, Randomized, Placebo-Controlled Trial","authors":"Yumin Zhou , Fan Wu , Haiqing Li , Zhishan Deng , Li Lin , Hong Huang , Haiyan Zhao , Yiran Wang , Lingwei Wang , Qijian Cheng , Shan Cai , Zhiyi He , Yinghua Ying , Peiyu Huang , Heshen Tian , Jieqi Peng , Shan Xiao , Xiang Wen , Huajing Yang , Youlan Zhen , Pixin Ran","doi":"10.1016/j.arbres.2025.01.004","DOIUrl":null,"url":null,"abstract":"<div><h3>Objectives</h3><div><span>Carbocysteine can reduce the frequency of acute exacerbations and improve respiratory symptoms to a certain extent in severe to very severe </span>chronic obstructive pulmonary disease<span> (COPD) patients. The objective of the study was to evaluate the efficacy of carbocysteine on the rate of exacerbations and pulmonary function for mild-to-moderate COPD patients.</span></div></div><div><h3>Methods</h3><div>In this phase 4, multicenter, double-blind, randomized, placebo-controlled, parallel-group trial, we randomly assigned mild-to-moderate COPD patients in a 2:1 ratio to treatment with carbocysteine (500<!--> <!-->mg, thrice daily) or matched placebo for 12 months. Eligible participants were 40–80 years of age. The coprimary outcomes were the annual rate of exacerbations of COPD (mild, moderate or severe) during the 12-month trial period or the difference in the FEV<sub>1</sub><span> before bronchodilator use at 12-month from baseline.</span></div></div><div><h3>Results</h3><div><span><span><span><span>Owing to slower-than-anticipated recruitment caused by the COVID-19 pandemic, recruitment of an estimated sample size of 732 patients stopped after 539 patients. The sample size was indeed reached for the annual rate of exacerbations but not for </span>pulmonary function. Among 539 patients, </span>362 were randomized to receive carbocysteine and </span>177 to receive matched placebo. There was no significant difference in the annual rate of exacerbations of COPD between carbocysteine group and placebo group (0.39 vs. 0.46 per patient year; relative risk [RR], 0.85; 95% confidence interval [CI], 0.64–1.13; </span><em>P</em> <!-->=<!--> <!-->0.273). Based on the available sample size, the difference in the change of FEV<sub>1</sub><span> before bronchodilator use at 12 months between carbocysteine group and placebo group has not been observed (46</span> <!-->±<!--> <!-->12 vs. 50<!--> <!-->±<!--> <!-->17<!--> <!-->ml; mean difference, 6 ml; 95% CI, −24 to 36; adjusted <em>P</em> <!-->=<!--> <!-->0.700).</div></div><div><h3>Conclusions</h3><div>Our findings suggested that carbocysteine might not significantly reduce the annual rate of total exacerbations in patients with mild-to-moderate COPD. The findings may have been compromised by an overestimation of the efficacy of carbocysteine on reducing exacerbations in mild-to-moderate COPD and potential confounding by baseline imbalances. The efficacy on lung function could not be adequately evaluated.</div><div>Clinical trial registered with Chictr.org.cn (ChiCTR1800016712).</div></div>","PeriodicalId":8339,"journal":{"name":"Archivos De Bronconeumologia","volume":"61 9","pages":"Pages 528-535"},"PeriodicalIF":9.2000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archivos De Bronconeumologia","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0300289625000109","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RESPIRATORY SYSTEM","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives
Carbocysteine can reduce the frequency of acute exacerbations and improve respiratory symptoms to a certain extent in severe to very severe chronic obstructive pulmonary disease (COPD) patients. The objective of the study was to evaluate the efficacy of carbocysteine on the rate of exacerbations and pulmonary function for mild-to-moderate COPD patients.
Methods
In this phase 4, multicenter, double-blind, randomized, placebo-controlled, parallel-group trial, we randomly assigned mild-to-moderate COPD patients in a 2:1 ratio to treatment with carbocysteine (500 mg, thrice daily) or matched placebo for 12 months. Eligible participants were 40–80 years of age. The coprimary outcomes were the annual rate of exacerbations of COPD (mild, moderate or severe) during the 12-month trial period or the difference in the FEV1 before bronchodilator use at 12-month from baseline.
Results
Owing to slower-than-anticipated recruitment caused by the COVID-19 pandemic, recruitment of an estimated sample size of 732 patients stopped after 539 patients. The sample size was indeed reached for the annual rate of exacerbations but not for pulmonary function. Among 539 patients, 362 were randomized to receive carbocysteine and 177 to receive matched placebo. There was no significant difference in the annual rate of exacerbations of COPD between carbocysteine group and placebo group (0.39 vs. 0.46 per patient year; relative risk [RR], 0.85; 95% confidence interval [CI], 0.64–1.13; P = 0.273). Based on the available sample size, the difference in the change of FEV1 before bronchodilator use at 12 months between carbocysteine group and placebo group has not been observed (46 ± 12 vs. 50 ± 17 ml; mean difference, 6 ml; 95% CI, −24 to 36; adjusted P = 0.700).
Conclusions
Our findings suggested that carbocysteine might not significantly reduce the annual rate of total exacerbations in patients with mild-to-moderate COPD. The findings may have been compromised by an overestimation of the efficacy of carbocysteine on reducing exacerbations in mild-to-moderate COPD and potential confounding by baseline imbalances. The efficacy on lung function could not be adequately evaluated.
Clinical trial registered with Chictr.org.cn (ChiCTR1800016712).
期刊介绍:
Archivos de Bronconeumologia is a scientific journal that specializes in publishing prospective original research articles focusing on various aspects of respiratory diseases, including epidemiology, pathophysiology, clinical practice, surgery, and basic investigation. Additionally, the journal features other types of articles such as reviews, editorials, special articles of interest to the society and editorial board, scientific letters, letters to the editor, and clinical images. Published monthly, the journal comprises 12 regular issues along with occasional supplements containing articles from different sections.
All manuscripts submitted to the journal undergo rigorous evaluation by the editors and are subjected to expert peer review. The editorial team, led by the Editor and/or an Associate Editor, manages the peer-review process. Archivos de Bronconeumologia is published monthly in English, facilitating broad dissemination of the latest research findings in the field.