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Effect of Erdosteine on COPD Exacerbations in COPD Patients with Moderate Airflow Limitation
BACKGROUND: The RESTORE study, a multi-national randomized, placebo-controlled study, showed that erdosteine – a muco-active antioxidant that modulates bacterial adhesiveness – reduced the rate and duration of exacerbations in moderate and severe COPD with a history of exacerbations. How much benefi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896911/ https://www.ncbi.nlm.nih.gov/pubmed/31819405 http://dx.doi.org/10.2147/COPD.S221852 |
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author | Calverley, Peter MA Page, Clive Dal Negro, Roberto W Fontana, Giovanni Cazzola, Mario Cicero, Arrigo F Pozzi, Edoardo Wedzicha, Jadwiga A |
author_facet | Calverley, Peter MA Page, Clive Dal Negro, Roberto W Fontana, Giovanni Cazzola, Mario Cicero, Arrigo F Pozzi, Edoardo Wedzicha, Jadwiga A |
author_sort | Calverley, Peter MA |
collection | PubMed |
description | BACKGROUND: The RESTORE study, a multi-national randomized, placebo-controlled study, showed that erdosteine – a muco-active antioxidant that modulates bacterial adhesiveness – reduced the rate and duration of exacerbations in moderate and severe COPD with a history of exacerbations. How much benefit patients with less severe disease experience when taking this drug remains unclear. METHODS: This post hoc analysis of the 254 RESTORE participants with spirometrically-defined moderate COPD (post-bronchodilator forced expiratory volume in 1 second [FEV(1)] 50‒79% predicted) examined exacerbation rate and duration, time to first exacerbation, and exacerbation-free time. Data were analyzed using descriptive statistics and comparisons between treatment groups used Wilcoxon rank-sum tests, Mann–Whitney U-tests, or log rank tests. RESULTS: Patients with moderate COPD received erdosteine 300 mg twice daily (n=126) or placebo (n=128) added to usual COPD therapy for 12 months. During this time, there were 53 exacerbations in the erdosteine group and 74 in the placebo group, with 42.1% and 57.8% of patients, respectively, experiencing an exacerbation. There was a 47% reduction in the mean exacerbation rate with erdosteine compared to placebo (0.27 vs 0.51 exacerbations per-patient per-year, respectively, P=0.003), and a 58.3% reduction in the mild exacerbation rate (0.23 vs 0.53 mild exacerbations per-patient per-year, P=0.001). Mean duration of exacerbations was 26% shorter in erdosteine-treated patients (9.1 vs 12.3 days for placebo, P=0.022), with significant reductions in the duration of mild and moderate-to-severe exacerbations. Mean time to first exacerbation was prolonged by 7.7% (182 days for erdosteine vs 169 days for placebo, P<0.001) and the mean exacerbation-free time was increased by 51 days (279 days for erdosteine vs 228 days for placebo; P<0.001). CONCLUSION: These results indicate that adding erdosteine to usual COPD maintenance therapy reduces the number of mild, and duration of all, exacerbations in patients with moderate COPD and a history of exacerbations. |
format | Online Article Text |
id | pubmed-6896911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-68969112019-12-09 Effect of Erdosteine on COPD Exacerbations in COPD Patients with Moderate Airflow Limitation Calverley, Peter MA Page, Clive Dal Negro, Roberto W Fontana, Giovanni Cazzola, Mario Cicero, Arrigo F Pozzi, Edoardo Wedzicha, Jadwiga A Int J Chron Obstruct Pulmon Dis Clinical Trial Report BACKGROUND: The RESTORE study, a multi-national randomized, placebo-controlled study, showed that erdosteine – a muco-active antioxidant that modulates bacterial adhesiveness – reduced the rate and duration of exacerbations in moderate and severe COPD with a history of exacerbations. How much benefit patients with less severe disease experience when taking this drug remains unclear. METHODS: This post hoc analysis of the 254 RESTORE participants with spirometrically-defined moderate COPD (post-bronchodilator forced expiratory volume in 1 second [FEV(1)] 50‒79% predicted) examined exacerbation rate and duration, time to first exacerbation, and exacerbation-free time. Data were analyzed using descriptive statistics and comparisons between treatment groups used Wilcoxon rank-sum tests, Mann–Whitney U-tests, or log rank tests. RESULTS: Patients with moderate COPD received erdosteine 300 mg twice daily (n=126) or placebo (n=128) added to usual COPD therapy for 12 months. During this time, there were 53 exacerbations in the erdosteine group and 74 in the placebo group, with 42.1% and 57.8% of patients, respectively, experiencing an exacerbation. There was a 47% reduction in the mean exacerbation rate with erdosteine compared to placebo (0.27 vs 0.51 exacerbations per-patient per-year, respectively, P=0.003), and a 58.3% reduction in the mild exacerbation rate (0.23 vs 0.53 mild exacerbations per-patient per-year, P=0.001). Mean duration of exacerbations was 26% shorter in erdosteine-treated patients (9.1 vs 12.3 days for placebo, P=0.022), with significant reductions in the duration of mild and moderate-to-severe exacerbations. Mean time to first exacerbation was prolonged by 7.7% (182 days for erdosteine vs 169 days for placebo, P<0.001) and the mean exacerbation-free time was increased by 51 days (279 days for erdosteine vs 228 days for placebo; P<0.001). CONCLUSION: These results indicate that adding erdosteine to usual COPD maintenance therapy reduces the number of mild, and duration of all, exacerbations in patients with moderate COPD and a history of exacerbations. Dove 2019-12-02 /pmc/articles/PMC6896911/ /pubmed/31819405 http://dx.doi.org/10.2147/COPD.S221852 Text en © 2019 Calverley et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Clinical Trial Report Calverley, Peter MA Page, Clive Dal Negro, Roberto W Fontana, Giovanni Cazzola, Mario Cicero, Arrigo F Pozzi, Edoardo Wedzicha, Jadwiga A Effect of Erdosteine on COPD Exacerbations in COPD Patients with Moderate Airflow Limitation |
title | Effect of Erdosteine on COPD Exacerbations in COPD Patients with Moderate Airflow Limitation |
title_full | Effect of Erdosteine on COPD Exacerbations in COPD Patients with Moderate Airflow Limitation |
title_fullStr | Effect of Erdosteine on COPD Exacerbations in COPD Patients with Moderate Airflow Limitation |
title_full_unstemmed | Effect of Erdosteine on COPD Exacerbations in COPD Patients with Moderate Airflow Limitation |
title_short | Effect of Erdosteine on COPD Exacerbations in COPD Patients with Moderate Airflow Limitation |
title_sort | effect of erdosteine on copd exacerbations in copd patients with moderate airflow limitation |
topic | Clinical Trial Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896911/ https://www.ncbi.nlm.nih.gov/pubmed/31819405 http://dx.doi.org/10.2147/COPD.S221852 |
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