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利妥昔单抗治疗系统性硬化病(SSc)患者的疗效和安全性:系统评价和荟萃分析。

Efficacy and safety of rituximab therapy in patients with systemic sclerosis disease (SSc): systematic review and meta-analysis.

机构信息

Golestan Rheumatology Research Center, Golestan University of Medical Sciences, Gorgan, Iran.

Department of Biostatistics, Faculty of Health, Hamadan University of Medical Sciences, Hamadan, Iran.

出版信息

Clin Rheumatol. 2021 Oct;40(10):3897-3918. doi: 10.1007/s10067-021-05698-4. Epub 2021 Apr 2.

Abstract

The clinical benefits of rituximab in systemic sclerosis (SSc) are still contentious. The present meta-analysis aimed to systematically assess rituximab's safety and efficacy profile in SSc patients. A systematic online query was performed in PubMed, Scopus, Web of Science, and Embase. The studies on the application of rituximab for patients with SSc were reviewed comprehensively for over two years. In terms of efficacy profile, mRSS, MS, LVEF, sPAP, FVC, DLCO, TLC, FEV, DAS, severity activity, HAQ-DI and SF36 were assessed for organ involvement and quality of life. The level of biological and immunological markers was also evaluated in SSc patients treated with RTX. In total, 24 studies met the criteria. Although they did not have a high quality, they were free from heterogeneity and publication bias. The pooled results revealed a long-term improvement in mRSS and MS. HAQ-DI was improved to 0.78 after 12 months, and DAS was significantly reduced to 0.33, 0.23, and 0.24 following 6, 12, and 24 months of treatment, respectively (p = 0.00 for both parameters). The rest of the parameters remained stable over time in patients with SSc. The pooled analysis of these patients demonstrated that the induction of death, cancer, infection, and infusion were 9, 5, 18 and 10%, respectively. Based on the pooled results of this meta-analysis, rituximab improves skin score and disease indices and stabilizes organ involvement in SSc patients. Rituximab seems to possess reasonable safety, similar to previous data from other autoimmune diseases.

摘要

利妥昔单抗在系统性硬化症(SSc)中的临床获益仍存在争议。本荟萃分析旨在系统评估利妥昔单抗在 SSc 患者中的安全性和疗效特征。在 PubMed、Scopus、Web of Science 和 Embase 上进行了系统的在线检索。对超过两年内应用利妥昔单抗治疗 SSc 患者的研究进行了全面综述。在疗效特征方面,评估了 mRSS、MS、LVEF、sPAP、FVC、DLCO、TLC、FEV、DAS、严重程度活动、HAQ-DI 和 SF36 等器官受累和生活质量指标。还评估了 SSc 患者接受 RTX 治疗后生物和免疫标志物的水平。共有 24 项研究符合标准。尽管它们的质量不高,但没有异质性和发表偏倚。汇总结果显示 mRSS 和 MS 长期改善。12 个月后 HAQ-DI 改善至 0.78,6、12 和 24 个月时 DAS 分别显著降低至 0.33、0.23 和 0.24(均为 p = 0.00)。在 SSc 患者中,其余参数随时间保持稳定。对这些患者的汇总分析表明,诱导死亡、癌症、感染和输注的发生率分别为 9%、5%、18%和 10%。基于这项荟萃分析的汇总结果,利妥昔单抗改善了 SSc 患者的皮肤评分和疾病指标,并稳定了器官受累。利妥昔单抗似乎具有合理的安全性,与其他自身免疫性疾病的先前数据相似。

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