One-year clinical experience on the use of Nintedanib in systemic sclerosis

被引:0
作者
Magnani, Luca [1 ]
Spinella, Amelia [2 ]
Testoni, Sofia [1 ,2 ]
Lumetti, Federica [2 ]
Scelfo, Chiara [3 ]
Dardani, Lucia [1 ]
Bajocchi, Gianluigi [1 ]
Clini, Enrico [4 ]
Salvarani, Carlo [1 ,2 ]
Giuggioli, Dilia [2 ,5 ]
机构
[1] AUSL IRCCS Reggio Emilia, Rheumatol Unit, Reggio Emilia, Italy
[2] Univ Modena & Reggio Emilia AOU Modena, Scleroderma Unit, Rheumatol, VIA POZZO 71, I-41100 Modena, Italy
[3] AUSL IRCSS Reggio Emilia, Pneumol Unit, Reggio Emilia, Italy
[4] Univ Modena & Reggio Emilia, Dept Med & Surg Sci Children & Adult, Resp Dis Unit, Pneumol, Reggio Emilia, Italy
[5] Univ Modena & Reggio E, Policlin Modena, Dept Med & Surg Sci Children & Adult, Rheumatol Unit, Via Pozzo 71, I-41100 Modena, Italy
来源
RESPIROLOGY CASE REPORTS | 2023年 / 11卷 / 06期
关键词
autoimmunity; fibrosis; interstitial lung disease; rare disease; systemic sclerosis; CLASSIFICATION; SCLERODERMA;
D O I
10.1002/rcr2.1120
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
We reviewed 11 patients with systemic sclerosis-related ILD who were referred to our Scleroderma Unit from January 2020 to January 2021 and started Nintedanib. Non-specific interstitial pneumonia (NSIP) was prevalent (45%), usual interstitial pneumonia (UIP) and UIP/NSIP pattern were both 27%. Only one patient had a history of smoking. Eight patients were on mycophenolate mofetil (MMF), eight were treated with corticosteroids (mean dose 5 mg/day of Prednisone or equivalent), and three were on Rituximab. The mean modified British Council Medical Questionnaire (mmRC) decreased from 3 to 2.5. Two patients had to reduce their daily dose to 200 mg/day for severe diarrhoea. Nintedanib was generally well tolerated.
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页数:4
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