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The efficacy and safety of rituximab in treating childhood refractory nephrotic syndrome: A meta-analysis

机译:利妥昔单抗治疗儿童难治性肾病综合征的疗效和安全性的荟萃分析

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Rituximab is considered to be a promising drug for treating childhood refractory nephrotic syndrome. However, the efficacy and safety of rituximab in treating childhood refractory nephrotic syndrome remain inconclusive. This meta-analysis aimed to investigate the efficacy and safety of rituximab treatment compared with other immunosuppressive agents in children with refractory nephrotic syndrome. Three randomized controlled trials and two comparative control studies were included in our analysis. The included studies were of moderately high quality. Compared with other immunotherapies, rituximab therapy significantly improved relapse-free survival (hazard ratio = 0.49, 95% confidence interval [CI], 0.26–0.92, P = 0.03). Rituximab also achieved a higher rate of complete remission (risk ratio,1.62; 95% CI, 0.92 to 2.84, P = 0.09) and reduced the occurrence of proteinuria (mean difference = ?0.25, 95% CI = ?0.29 to ?0.21, P
机译:利妥昔单抗被认为是治疗儿童难治性肾病综合征的有前途的药物。然而,利妥昔单抗治疗儿童难治性肾病综合征的疗效和安全性尚无定论。这项荟萃分析旨在研究与难治性肾病综合征儿童相比,利妥昔单抗治疗与其他免疫抑制剂相比的疗效和安全性。我们的分析包括三项随机对照试验和两项比较性对照研究。纳入的研究质量中等。与其他免疫疗法相比,利妥昔单抗疗法显着改善了无复发生存率(危险比= 0.49,95%置信区间[CI],0.26-0.92,P = 0.03)。利妥昔单抗的完全缓解率更高(风险比为1.62; 95%CI为0.92至2.84,P = 0.09),并减少了蛋白尿的发生(平均差异= 0.25,95%CI = 0.29至0.21, P

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