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Etanercept/celecoxib on improving MRI inflammation of active ankylosing spondylitis: A multicenter, open-label, randomized clinical trial

OBJECTIVE: To investigate the efficacy and safety of clinical, magnetic resonance imaging (MRI) changes in active ankylosing spondylitis (AS) patients with etanercept and celecoxib alone/combined treatment. METHODS: A randomized controlled trial was conducted in three medical centers in China. Adult...

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Autores principales: Tu, Liudan, Zhao, Minjing, Wang, Xiaohong, Kong, Qingcong, Chen, Zena, Wei, Qiujing, Li, Qiuxia, Yu, Qinghong, Ye, Zhizhong, Cao, Shuangyan, Lin, Zhimin, Liao, Zetao, Lv, Qing, Qi, Jun, Jin, Ou, Pan, Yunfeng, Gu, Jieruo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458864/
https://www.ncbi.nlm.nih.gov/pubmed/36091030
http://dx.doi.org/10.3389/fimmu.2022.967658
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author Tu, Liudan
Zhao, Minjing
Wang, Xiaohong
Kong, Qingcong
Chen, Zena
Wei, Qiujing
Li, Qiuxia
Yu, Qinghong
Ye, Zhizhong
Cao, Shuangyan
Lin, Zhimin
Liao, Zetao
Lv, Qing
Qi, Jun
Jin, Ou
Pan, Yunfeng
Gu, Jieruo
author_facet Tu, Liudan
Zhao, Minjing
Wang, Xiaohong
Kong, Qingcong
Chen, Zena
Wei, Qiujing
Li, Qiuxia
Yu, Qinghong
Ye, Zhizhong
Cao, Shuangyan
Lin, Zhimin
Liao, Zetao
Lv, Qing
Qi, Jun
Jin, Ou
Pan, Yunfeng
Gu, Jieruo
author_sort Tu, Liudan
collection PubMed
description OBJECTIVE: To investigate the efficacy and safety of clinical, magnetic resonance imaging (MRI) changes in active ankylosing spondylitis (AS) patients with etanercept and celecoxib alone/combined treatment. METHODS: A randomized controlled trial was conducted in three medical centers in China. Adult AS patients with BASDAI ≥4 or ASDAS ≥2.1, CRP >6 mg/L, or ESR 28 mm/1st hour were randomly assigned (1:1:1 ratio) to celecoxib 200 mg bid or etanercept 50 mg qw or combined therapy for 52 weeks. The primary outcomes were SPARCC change of the sacroiliac joint (SIJ) and spine and the proportion of patients achieving ASAS20 response at 52 weeks. RESULTS: Between September 2014 and January 2016, we randomly assigned 150 patients (mean age, 32.4 years; mean disease duration, 109 months), and 133 (88.6%) completed the study. SPARCC inflammation scores of the SIJ and spine decreased in the three groups, and significant differences were found between the combined group and the celecoxib group [between-group difference: −6.33, 95% CI (−10.56, −2.10) for SIJ; −9.53, 95% CI (−13.73, −5.33) for spine] and between the etanercept group and the celecoxib group [between-group difference: −5.02, 95% CI (−9.29, −0.76) for SIJ; −5.80, 95% CI (−10.04, −1.57) for spine]. The ASAS20 response rates were 44%, 58%, and 84% in the celecoxib, etanercept, and combined groups, respectively, and a significant difference was only found between the combined and the celecoxib groups. CONCLUSION: Etanercept with or without celecoxib decreases inflammation detected by MRI at 1 year compared to celecoxib alone in active AS patients. The combination of etanercept and celecoxib was superior to celecoxib alone for the primary clinical response. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov, identifier NCT01934933.
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spelling pubmed-94588642022-09-10 Etanercept/celecoxib on improving MRI inflammation of active ankylosing spondylitis: A multicenter, open-label, randomized clinical trial Tu, Liudan Zhao, Minjing Wang, Xiaohong Kong, Qingcong Chen, Zena Wei, Qiujing Li, Qiuxia Yu, Qinghong Ye, Zhizhong Cao, Shuangyan Lin, Zhimin Liao, Zetao Lv, Qing Qi, Jun Jin, Ou Pan, Yunfeng Gu, Jieruo Front Immunol Immunology OBJECTIVE: To investigate the efficacy and safety of clinical, magnetic resonance imaging (MRI) changes in active ankylosing spondylitis (AS) patients with etanercept and celecoxib alone/combined treatment. METHODS: A randomized controlled trial was conducted in three medical centers in China. Adult AS patients with BASDAI ≥4 or ASDAS ≥2.1, CRP >6 mg/L, or ESR 28 mm/1st hour were randomly assigned (1:1:1 ratio) to celecoxib 200 mg bid or etanercept 50 mg qw or combined therapy for 52 weeks. The primary outcomes were SPARCC change of the sacroiliac joint (SIJ) and spine and the proportion of patients achieving ASAS20 response at 52 weeks. RESULTS: Between September 2014 and January 2016, we randomly assigned 150 patients (mean age, 32.4 years; mean disease duration, 109 months), and 133 (88.6%) completed the study. SPARCC inflammation scores of the SIJ and spine decreased in the three groups, and significant differences were found between the combined group and the celecoxib group [between-group difference: −6.33, 95% CI (−10.56, −2.10) for SIJ; −9.53, 95% CI (−13.73, −5.33) for spine] and between the etanercept group and the celecoxib group [between-group difference: −5.02, 95% CI (−9.29, −0.76) for SIJ; −5.80, 95% CI (−10.04, −1.57) for spine]. The ASAS20 response rates were 44%, 58%, and 84% in the celecoxib, etanercept, and combined groups, respectively, and a significant difference was only found between the combined and the celecoxib groups. CONCLUSION: Etanercept with or without celecoxib decreases inflammation detected by MRI at 1 year compared to celecoxib alone in active AS patients. The combination of etanercept and celecoxib was superior to celecoxib alone for the primary clinical response. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov, identifier NCT01934933. Frontiers Media S.A. 2022-08-26 /pmc/articles/PMC9458864/ /pubmed/36091030 http://dx.doi.org/10.3389/fimmu.2022.967658 Text en Copyright © 2022 Tu, Zhao, Wang, Kong, Chen, Wei, Li, Yu, Ye, Cao, Lin, Liao, Lv, Qi, Jin, Pan and Gu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Tu, Liudan
Zhao, Minjing
Wang, Xiaohong
Kong, Qingcong
Chen, Zena
Wei, Qiujing
Li, Qiuxia
Yu, Qinghong
Ye, Zhizhong
Cao, Shuangyan
Lin, Zhimin
Liao, Zetao
Lv, Qing
Qi, Jun
Jin, Ou
Pan, Yunfeng
Gu, Jieruo
Etanercept/celecoxib on improving MRI inflammation of active ankylosing spondylitis: A multicenter, open-label, randomized clinical trial
title Etanercept/celecoxib on improving MRI inflammation of active ankylosing spondylitis: A multicenter, open-label, randomized clinical trial
title_full Etanercept/celecoxib on improving MRI inflammation of active ankylosing spondylitis: A multicenter, open-label, randomized clinical trial
title_fullStr Etanercept/celecoxib on improving MRI inflammation of active ankylosing spondylitis: A multicenter, open-label, randomized clinical trial
title_full_unstemmed Etanercept/celecoxib on improving MRI inflammation of active ankylosing spondylitis: A multicenter, open-label, randomized clinical trial
title_short Etanercept/celecoxib on improving MRI inflammation of active ankylosing spondylitis: A multicenter, open-label, randomized clinical trial
title_sort etanercept/celecoxib on improving mri inflammation of active ankylosing spondylitis: a multicenter, open-label, randomized clinical trial
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458864/
https://www.ncbi.nlm.nih.gov/pubmed/36091030
http://dx.doi.org/10.3389/fimmu.2022.967658
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