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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...

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Detalles Bibliográficos
Autores principales: Gan, C.Tji-Joong, Ward, Chris, Meachery, Gerard, Lordan, James Laurence, Fisher, Andrew J, Corris, Paul A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
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
Descripción
Sumario: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.