Intravenous cyclophosphamidevsrituximab for the treatment of early diffuse scleroderma lung disease: open label, randomized, controlled trial

医学 美罗华 硬皮病(真菌) 环磷酰胺 间质性肺病 打开标签 随机对照试验 内科学 病理 化疗 淋巴瘤 接种
作者
Geetabali Sircar,Rudra Prosad Goswami,Dipankar Sircar,Alakendu Ghosh,Parasar Ghosh
出处
期刊:Rheumatology [Oxford University Press]
卷期号:57 (12): 2106-2113 被引量:195
标识
DOI:10.1093/rheumatology/key213
摘要

SSc is characterized by fibrotic changes in the skin and lung, and the mainstay of treatment has been CYC. B cell involvement suggests that rituximab (RTX) may also be of therapeutic benefit. The aim of the study was to compare the efficacy and safety of RTX compared with CYC in retarding the progression of interstitial lung disease and skin manifestations of primary SSc.We randomly assigned 60 patients of dcSSc, age 18-60 years with skin and lung involvement, to monthly pulses of CYC 500 mg/m2 or RTX 1000 mg × 2 doses at 0, 15 days. Primary outcomes were forced vital capacity (FVC) percent predicted at 6 months. Secondary outcomes were: absolute change in litres (FVC-l) at 6 months; modified Rodnan skin scores at 6 months, 6-min walk test, Medsgers score and new onset or worsening of existing pulmonary hypertension by echocardiographic criteria.The FVC [%mean (s.d.)] in the RTX group improved from 61.30 (11.28) to 67.52 (13.59), while in the CYC group it declined from 59.25 (12.96) to 58.06 (11.23) at 6 months (P = 0.003). The change of FVC was 1.51 (0.45) l to 1.65 (0.47) l in the RTX group, compared with 1.42 (0.49) to 1.42 (0.46) l in the CYC group. The mRSS changed from 21.77 (9.86) to 12.10 (10.14) in the RTX group and 23.83 (9.28) to 18.33 (7.69) in the CYC group after 6 months. Serious adverse events were more common in the CYC group.RTX is a safe and effective alternative to CYC in the primary therapy of skin and lung manifestations of scleroderma.Clinical Trials Registry - India, www.ctri.nic.in, CTRI/2017/07/009152.
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