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A Real-World Study on the Effect of Imrecoxib for Patients with Axial Spondyloarthritis
PURPOSE: Non-steroidal anti-inflammatory drugs (NSAIDs) have generally been viewed as first-line therapy for axial spondyloarthritis (axSpA). Imrecoxib is a selective COX-2 inhibitor developed independently in China. At present, only one single-center RCT trial has shown that imrecoxib is equally ef...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416422/ https://www.ncbi.nlm.nih.gov/pubmed/36033132 http://dx.doi.org/10.2147/DDDT.S376406 |
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author | Zong, He-xiang Xu, Sheng-qian Wang, Jian-xiong Chu, Yi-ran Chen, Ke-ming Wang, Cong Tong, Wan-qiu Wang, Xi-le |
author_facet | Zong, He-xiang Xu, Sheng-qian Wang, Jian-xiong Chu, Yi-ran Chen, Ke-ming Wang, Cong Tong, Wan-qiu Wang, Xi-le |
author_sort | Zong, He-xiang |
collection | PubMed |
description | PURPOSE: Non-steroidal anti-inflammatory drugs (NSAIDs) have generally been viewed as first-line therapy for axial spondyloarthritis (axSpA). Imrecoxib is a selective COX-2 inhibitor developed independently in China. At present, only one single-center RCT trial has shown that imrecoxib is equally effective as celecoxib in treating axSpA. Based on real-world data, our study aims to explore the efficiency of imrecoxib and TNF inhibitor (TNFi) combined with imrecoxib in treating axSpA. PATIENTS AND METHODS: A total of 163 patients with axSpA who had more than two follow-up records in 6 months and treated with imrecoxib/celecoxib/TNFi combined with imrecoxib/TNFi combined with celecoxib from the First Affiliated Hospital of Anhui Medical University SpA Real World Database (AHSpA) were selected for analysis of our study. The linear mixed model was used to compare efficacy indexes before and after treatment and between different groups, adjust baseline measurement value and follow-up time. The Kaplan–Meier survival analysis was used to identify the differences in cumulative clinical remission rates between groups with different treatment at the follow-up period. RESULTS: Results showed that after treatment ASDAScrp was slightly improved in imrecoxib group and celecoxib group within 6 months (p < 0.05). CRP, ESR, BASDAI, ASDAScrp, BASFI, occiput to wall distance and finger floor distance all significantly improved in TNFi combined with imrecoxib group and TNFi combined with celecoxib group within 6 months (all p < 0.05). According to the Kaplan–Meier survival curve and Log rank test analysis, the clinical remission rate was not significantly different between different treatment during 24-month follow-up (all p > 0.05). CONCLUSION: ASDAScrp improved slightly within 6 months after treatment with imrecoxib, and TNFi combined with imrecoxib significantly improved multiple effect indexes in axSpA patients. The efficacy of imrecoxib and celecoxib in the treatment of axSpA is equivalent. Also, they have the same efficacy after being combined with TNFi. |
format | Online Article Text |
id | pubmed-9416422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-94164222022-08-27 A Real-World Study on the Effect of Imrecoxib for Patients with Axial Spondyloarthritis Zong, He-xiang Xu, Sheng-qian Wang, Jian-xiong Chu, Yi-ran Chen, Ke-ming Wang, Cong Tong, Wan-qiu Wang, Xi-le Drug Des Devel Ther Original Research PURPOSE: Non-steroidal anti-inflammatory drugs (NSAIDs) have generally been viewed as first-line therapy for axial spondyloarthritis (axSpA). Imrecoxib is a selective COX-2 inhibitor developed independently in China. At present, only one single-center RCT trial has shown that imrecoxib is equally effective as celecoxib in treating axSpA. Based on real-world data, our study aims to explore the efficiency of imrecoxib and TNF inhibitor (TNFi) combined with imrecoxib in treating axSpA. PATIENTS AND METHODS: A total of 163 patients with axSpA who had more than two follow-up records in 6 months and treated with imrecoxib/celecoxib/TNFi combined with imrecoxib/TNFi combined with celecoxib from the First Affiliated Hospital of Anhui Medical University SpA Real World Database (AHSpA) were selected for analysis of our study. The linear mixed model was used to compare efficacy indexes before and after treatment and between different groups, adjust baseline measurement value and follow-up time. The Kaplan–Meier survival analysis was used to identify the differences in cumulative clinical remission rates between groups with different treatment at the follow-up period. RESULTS: Results showed that after treatment ASDAScrp was slightly improved in imrecoxib group and celecoxib group within 6 months (p < 0.05). CRP, ESR, BASDAI, ASDAScrp, BASFI, occiput to wall distance and finger floor distance all significantly improved in TNFi combined with imrecoxib group and TNFi combined with celecoxib group within 6 months (all p < 0.05). According to the Kaplan–Meier survival curve and Log rank test analysis, the clinical remission rate was not significantly different between different treatment during 24-month follow-up (all p > 0.05). CONCLUSION: ASDAScrp improved slightly within 6 months after treatment with imrecoxib, and TNFi combined with imrecoxib significantly improved multiple effect indexes in axSpA patients. The efficacy of imrecoxib and celecoxib in the treatment of axSpA is equivalent. Also, they have the same efficacy after being combined with TNFi. Dove 2022-08-22 /pmc/articles/PMC9416422/ /pubmed/36033132 http://dx.doi.org/10.2147/DDDT.S376406 Text en © 2022 Zong et al. https://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/ (https://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 | Original Research Zong, He-xiang Xu, Sheng-qian Wang, Jian-xiong Chu, Yi-ran Chen, Ke-ming Wang, Cong Tong, Wan-qiu Wang, Xi-le A Real-World Study on the Effect of Imrecoxib for Patients with Axial Spondyloarthritis |
title | A Real-World Study on the Effect of Imrecoxib for Patients with Axial Spondyloarthritis |
title_full | A Real-World Study on the Effect of Imrecoxib for Patients with Axial Spondyloarthritis |
title_fullStr | A Real-World Study on the Effect of Imrecoxib for Patients with Axial Spondyloarthritis |
title_full_unstemmed | A Real-World Study on the Effect of Imrecoxib for Patients with Axial Spondyloarthritis |
title_short | A Real-World Study on the Effect of Imrecoxib for Patients with Axial Spondyloarthritis |
title_sort | real-world study on the effect of imrecoxib for patients with axial spondyloarthritis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416422/ https://www.ncbi.nlm.nih.gov/pubmed/36033132 http://dx.doi.org/10.2147/DDDT.S376406 |
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