A multicenter, open-label, comparative study of B-cell depletion therapy with Rituximab for systemic sclerosis-associated interstitial lung disease

被引:163
作者
Daoussis, Dimitrios [1 ]
Melissaropoulos, Konstantinos [1 ]
Sakellaropoulos, Georgios [5 ]
Antonopoulos, Ioannis [1 ]
Markatseli, Theodora E. [2 ]
Simopoulou, Theodora [3 ]
Georgiou, Panagiotis [4 ]
Andonopoulos, Andrew P. [1 ]
Drosos, Alexandros A. [2 ]
Sakkas, Lazaros [3 ]
Liossis, Stamatis-Nick [1 ]
机构
[1] Univ Patras, Med Sch, Div Rheumatol, Patras Univ Hosp,Dept Internal Med, Patras 26504, Greece
[2] Univ Ioannina, Med Sch, Ioannina Univ Hosp, Dept Rheumatol, Ioannina, Greece
[3] Univ Thessaly, Med Sch, Larissa Univ Hosp, Dept Rheumatol, Larisa, Greece
[4] Agios Andreas Dist Hosp, Dept Rheumatol, Patras, Greece
[5] Univ Patras, Dept Med Phys, Patras, Greece
关键词
Scleroderma; Systemic sclerosis; Rituximab; Interstitial lung disease; Fibrosis; B cells; MYCOPHENOLATE-MOFETIL; SKIN INVOLVEMENT; GENE-EXPRESSION; AUTOIMMUNITY; PATHOGENESIS; FIBROBLASTS; CYCLOPHOSPHAMIDE; LYMPHOCYTES; MECHANISMS; EXPERIENCE;
D O I
10.1016/j.semarthrit.2016.10.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Rituximab (RTX) may favorably affect lung function and skin fibrosis in patients with systemic sclerosis (SSc). We aimed to assess long-term efficacy and safety of RTX in SSc compared to standard treatment. Methods: A total of 51 patients with SSc-associated interstitial lung disease were recruited and treated with RTX (n = 33) or conventional treatment (n = 18). Median follow-up was 4 years (range: 1-7). Conventional treatment consisted of azathioprine (n = 2), methotrexate (n = 6), and mycophenolate mofetil (n = 10). Results: Patients in the RTX group showed an increase in FVC at 2 years (mean +/- SD of FVC: 80.60 +/- 21.21 vs 86.90 +/- 20.56 at baseline vs 2 years, respectively, p = 0.041 compared to baseline). In sharp contrast, patients in the control group had no change in FVC during the first 2 years of follow-up. At the 7 year time point the remaining patients in the RTX group (n = 5) had higher FVC compared to baseline (mean +/- SD of FVC: 91.60 +/- 14.81, p = 0.158 compared to baseline) in contrast to patients in the control group (n = 9) where FVC deteriorated (p < 0.01, compared to baseline). Direct comparison between the 2 groups showed a significant benefit for the RTX group in FVC (p = 0.013). Improvement of skin thickening was found in both the RTX and the standard treatment group; however, direct comparison between groups strongly favored RTX at all-time points. Adverse events were comparable between groups. Conclusions: Our data indicate that RTX has a beneficial effect on lung function and skin fibrosis in patients with SSc. Randomized controlled studies are highly needed. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:625 / 631
页数:7
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