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               <dc:title>Rituximab in the treatment of progressive interstitial lung disease associated with the antisynthetase syndrome</dc:title>
               <dc:creator>Narváez, Javier</dc:creator>
               <dc:creator>Cañadillas, Elena</dc:creator>
               <dc:creator>Castellví, Ivan</dc:creator>
               <dc:creator>Alegre, Juan José</dc:creator>
               <dc:creator>Vincens Zygmunt, Vanesa</dc:creator>
               <dc:creator>Bermudo, Guadalupe</dc:creator>
               <dc:creator>Vidal Montal, Paola</dc:creator>
               <dc:creator>Molina Molina, María</dc:creator>
               <dc:creator>Nolla Solé, Joan Miquel</dc:creator>
               <dc:subject>Malalties del pulmó</dc:subject>
               <dc:subject>Miositis</dc:subject>
               <dc:subject>Pulmonary diseases</dc:subject>
               <dc:subject>Myositis</dc:subject>
               <dc:description>Objective To assess the real-world, long-term effectiveness of rituximab (RTX) as a rescue therapy in patients with antisynthetase syndrome and progressive interstitial lung disease (ASS-ILD). Methods Multicentre observational retrospective longitudinal study of a cohort of patients with ASS-ILD that started treatment with RTX due to recurrent or ongoing progressive ILD despite therapy with glucocorticoids and immunosuppressants. Results Twenty-eight patients were analyzed. Examining the entire study population, before treatment with RTX the mean decline in %pFVC and %pDLCO from the ASS-ILD diagnosis to the initiation of RTX treatment (T0) was -6.44% and -14.85%, respectively. After six months of treatment, RTX reversed the decline in pulmonary function test (PFT) parameters: triangle%pFVC +6.29% (95% CI: -10.07 to 2.51; p=0.002 compared to T0) and triangle%pDLCO +6.15% (95% CI: -10.86 to -1.43; p=0.013). Twenty-four patients completed one year of therapy and 22 two years, maintaining the response in PFT: triangle%pFVC: +9.93% (95% CI: -15.61 to -4.25; p=0.002) and triangle%pDLCO: +7.66% (95% CI: -11.67 to -3.65; p&lt;0.001). In addition, there was a significant reduction in the median dose of prednisone, and it could be suspended in 18% of cases. In 33% of patients who required oxygen therapy at the start of treatment, it could be discontinued. The frequency of adverse events reached 28.5% of cases. Results Twenty-eight patients were analyzed. Examining the entire study population, before treatment with RTX the mean decline in %pFVC and %pDLCO from the ASS-ILD diagnosis to the initiation of RTX treatment (T0) was -6.44% and -14.85%, respectively. After six months of treatment, RTX reversed the decline in pulmonary function test (PFT) parameters: triangle%pFVC +6.29% (95% CI: -10.07 to 2.51; p=0.002 compared to T0) and triangle%pDLCO +6.15% (95% CI: -10.86 to -1.43; p=0.013). Twenty-four patients completed one year of therapy and 22 two years, maintaining the response in PFT: triangle%pFVC: +9.93% (95% CI: -15.61 to -4.25; p=0.002) and triangle%pDLCO: +7.66% (95% CI: -11.67 to -3.65; p&lt;0.001). In addition, there was a significant reduction in the median dose of prednisone, and it could be suspended in 18% of cases. In 33% of patients who required oxygen therapy at the start of treatment, it could be discontinued. The frequency of adverse events reached 28.5% of cases. Conclusion Based on our results, RTX appears to be effective as rescue therapy in most patients with recurrent or progressive ASS-ILD unresponsive to conventional treatment. The use of RTX was well tolerated in the majority of patients.</dc:description>
               <dc:date>2024-08-30T11:15:28Z</dc:date>
               <dc:date>2024-08-30T11:15:28Z</dc:date>
               <dc:date>2024-06-18</dc:date>
               <dc:date>2024-07-02T09:18:10Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:relation>Reproducció del document publicat a: https://doi.org/10.1186/s13075-024-03353-2</dc:relation>
               <dc:relation>Arthritis Research &amp; Therapy, 2024, vol. 26, num. 1</dc:relation>
               <dc:relation>https://doi.org/10.1186/s13075-024-03353-2</dc:relation>
               <dc:rights>cc by (c) Narváez, Javier et al, 2024</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Springer Science and Business Media LLC</dc:publisher>
               <dc:source>Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))</dc:source>
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