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Rituximab for rheumatoid arthritis-related interstitial lung disease: A systematic review and meta-analysis

Volume: 39 Issue: 2, June 2024 Publish Date: June 30, 2024
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Tarun Krishna Boppana ORCID
All India Institute of Medical Sciences, Pulmonary, Critical Care and Sleep Medicine, Delhi, India image/svg+xml
Saurabh Mittal ORCID
All India Institute of Medical Sciences, Pulmonary, Critical Care and Sleep Medicine, Delhi, India image/svg+xml
Karan Madan ORCID
All India Institute of Medical Sciences, Pulmonary, Critical Care and Sleep Medicine, Delhi, India image/svg+xml
Anant Mohan ORCID
All India Institute of Medical Sciences, Pulmonary, Critical Care and Sleep Medicine, Delhi, India image/svg+xml
Vijay Hadda ORCID
All India Institute of Medical Sciences, Pulmonary, Critical Care and Sleep Medicine, Delhi, India image/svg+xml
Randeep Guleria ORCID
All India Institute of Medical Sciences, Pulmonary, Critical Care and Sleep Medicine, Delhi, India image/svg+xml
Tarun Krishna Boppana, Saurabh Mittal, Karan Madan, Anant Mohan, Vijay Hadda, & Randeep Guleria. (2024). Rituximab for rheumatoid arthritis-related interstitial lung disease: A systematic review and meta-analysis. Archives of Rheumatology, 39(2), 317–329. https://doi.org/10.46497/ArchRheumatol.2024.10199
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Abstract

Objectives: This systematic review and meta-analysis aimed at summarizing the evidence of efficacy and safety of rituximab in rheumatoid arthritis-related interstitial lung disease (RA-ILD).

Materials and methods: PubMed and Embase databases were searched until June 22, 2022, to identify studies on RA-ILD treated with rituximab, confined to predefined inclusion and exclusion criteria. A systematic review and meta-analysis were performed on the included studies to assess the overall stabilization or improvement in ILD, changes in percent-predicted (%-predicted) forced vital capacity (FVC), and %-predicted diffusion capacity of lungs for carbon monoxide (DLCO) following rituximab therapy.

Results: A total of 15 studies (4 prospective and 11 retrospective studies) were included, with a total of 314 patients. There were 105 (60.7%) females out of 173 subjects for whom sex details were available from seven studies. The overall pooled proportion of patients with stabilization or improvement in ILD was 0.88 [95% confidence interval (CI): 0.76-0.96, p=0.02]. Rituximab improved FVC from baseline by 7.50% (95% CI: 1.35-13.65; p=0.02, fixed effect). Similarly, rituximab improved DLCO by 6.39% (95% CI: 1.366-14.43; p=0.12, random-effect). Two retrospective studies reported reduced mortality with rituximab therapy compared to tumor necrosis factor-alpha inhibitors.

Conclusion: Treatment with rituximab in RA-ILD was associated with a significant improvement in %-predicted FVC, as well as stabilization or improvement in ILD after one year of treatment.

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Article Info
Published In
Journal Archives of Rheumatology
Volume / Issue Vol. 39 No. 2 (2024): The Archives of Rheumatology
Pages 317-329
History
Published Online June 30, 2024
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Affiliations
1
Tarun Krishna Boppana ORCID
All India Institute of Medical Sciences, Pulmonary, Critical Care and Sleep Medicine, Delhi, India
2
Saurabh Mittal ORCID
All India Institute of Medical Sciences, Pulmonary, Critical Care and Sleep Medicine, Delhi, India
3
Karan Madan ORCID
All India Institute of Medical Sciences, Pulmonary, Critical Care and Sleep Medicine, Delhi, India
4
Anant Mohan ORCID
All India Institute of Medical Sciences, Pulmonary, Critical Care and Sleep Medicine, Delhi, India
5
Vijay Hadda ORCID
All India Institute of Medical Sciences, Pulmonary, Critical Care and Sleep Medicine, Delhi, India
6
Randeep Guleria ORCID
All India Institute of Medical Sciences, Pulmonary, Critical Care and Sleep Medicine, Delhi, India
Cite this Article
Tarun Krishna Boppana, Saurabh Mittal, Karan Madan, Anant Mohan, Vijay Hadda, & Randeep Guleria. (2024). Rituximab for rheumatoid arthritis-related interstitial lung disease: A systematic review and meta-analysis. Archives of Rheumatology, 39(2), 317–329. https://doi.org/10.46497/ArchRheumatol.2024.10199
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