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Long-term effect of azithromycin in bronchiolitis obliterans syndrome
INTRODUCTION: Azithromycin stabilises and improves lung function forced expiratory volume in one second (FEV(1)) in lung transplantation patients with bronchiolitis obliterans syndrome (BOS). A post hoc analysis was performed to assess the long-term effect of azithromycin on FEV(1), BOS progression...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797396/ https://www.ncbi.nlm.nih.gov/pubmed/31673366 http://dx.doi.org/10.1136/bmjresp-2019-000465 |
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author | Gan, C.Tji-Joong Ward, Chris Meachery, Gerard Lordan, James Laurence Fisher, Andrew J Corris, Paul A |
author_facet | Gan, C.Tji-Joong Ward, Chris Meachery, Gerard Lordan, James Laurence Fisher, Andrew J Corris, Paul A |
author_sort | Gan, C.Tji-Joong |
collection | PubMed |
description | INTRODUCTION: Azithromycin stabilises and improves lung function forced expiratory volume in one second (FEV(1)) in lung transplantation patients with bronchiolitis obliterans syndrome (BOS). A post hoc analysis was performed to assess the long-term effect of azithromycin on FEV(1), BOS progression and survival . METHODS: Eligible patients recruited for the initial randomised placebo-controlled trial received open-label azithromycin after 3 months and were followed up until 6 years after inclusion (n=45) to assess FEV(1), BOS free progression and overall survival. RESULTS: FEV(1) in the placebo group improved after open-label azithromycin and was comparable with the treatment group by 6 months. FEV(1) decreased after 1 and 5 years and was not different between groups. Patients (n=18) with rapid progression of BOS underwent total lymphoid irradiation (TLI). Progression-free survival (log-rank test p=0.40) and overall survival (log-rank test p=0.28) were comparable. Survival of patients with early BOS was similar to late-onset BOS (log-rank test p=0.74). DISCUSSION: Long-term treatment with azithromycin slows down the progression of BOS, although the effect of TLI may affect the observed attenuation of FEV(1) decline. BOS progression and long-term survival were not affected by randomisation to the placebo group, given the early cross-over to azithromycin and possibly due to TLI in case of further progression. Performing randomised placebo-controlled trials in lung transplantation patients with BOS with a blinded trial duration is feasible, effective and safe. |
format | Online Article Text |
id | pubmed-6797396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-67973962019-10-31 Long-term effect of azithromycin in bronchiolitis obliterans syndrome Gan, C.Tji-Joong Ward, Chris Meachery, Gerard Lordan, James Laurence Fisher, Andrew J Corris, Paul A BMJ Open Respir Res Lung Transplantation INTRODUCTION: Azithromycin stabilises and improves lung function forced expiratory volume in one second (FEV(1)) in lung transplantation patients with bronchiolitis obliterans syndrome (BOS). A post hoc analysis was performed to assess the long-term effect of azithromycin on FEV(1), BOS progression and survival . METHODS: Eligible patients recruited for the initial randomised placebo-controlled trial received open-label azithromycin after 3 months and were followed up until 6 years after inclusion (n=45) to assess FEV(1), BOS free progression and overall survival. RESULTS: FEV(1) in the placebo group improved after open-label azithromycin and was comparable with the treatment group by 6 months. FEV(1) decreased after 1 and 5 years and was not different between groups. Patients (n=18) with rapid progression of BOS underwent total lymphoid irradiation (TLI). Progression-free survival (log-rank test p=0.40) and overall survival (log-rank test p=0.28) were comparable. Survival of patients with early BOS was similar to late-onset BOS (log-rank test p=0.74). DISCUSSION: Long-term treatment with azithromycin slows down the progression of BOS, although the effect of TLI may affect the observed attenuation of FEV(1) decline. BOS progression and long-term survival were not affected by randomisation to the placebo group, given the early cross-over to azithromycin and possibly due to TLI in case of further progression. Performing randomised placebo-controlled trials in lung transplantation patients with BOS with a blinded trial duration is feasible, effective and safe. BMJ Publishing Group 2019-10-15 /pmc/articles/PMC6797396/ /pubmed/31673366 http://dx.doi.org/10.1136/bmjresp-2019-000465 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Lung Transplantation Gan, C.Tji-Joong Ward, Chris Meachery, Gerard Lordan, James Laurence Fisher, Andrew J Corris, Paul A Long-term effect of azithromycin in bronchiolitis obliterans syndrome |
title | Long-term effect of azithromycin in bronchiolitis obliterans syndrome |
title_full | Long-term effect of azithromycin in bronchiolitis obliterans syndrome |
title_fullStr | Long-term effect of azithromycin in bronchiolitis obliterans syndrome |
title_full_unstemmed | Long-term effect of azithromycin in bronchiolitis obliterans syndrome |
title_short | Long-term effect of azithromycin in bronchiolitis obliterans syndrome |
title_sort | long-term effect of azithromycin in bronchiolitis obliterans syndrome |
topic | Lung Transplantation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797396/ https://www.ncbi.nlm.nih.gov/pubmed/31673366 http://dx.doi.org/10.1136/bmjresp-2019-000465 |
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