Efficacy and Safety of Rituximab for the Treatment of Graves' Orbitopathy: A Meta-analysis of Randomized Controlled Trials

被引:31
作者
Shen, Wan-Chen [1 ,2 ]
Lee, Chia-Hwa [3 ,4 ,5 ]
Loh, El-Wui [6 ]
Hsieh, An-Tsz [7 ,8 ]
Chen, Lawrence [9 ]
Tam, Ka-Wai [6 ,10 ,11 ,12 ]
机构
[1] Taipei Med Univ, Shuang Ho Hosp, Dept Pharm, New Taipei, Taiwan
[2] Taipei Med Univ, Coll Pharm, Taipei, Taiwan
[3] Taipei Med Univ, Coll Med Sci & Technol, Sch Med Lab Sci & Biotechnol, Taipei, Taiwan
[4] Taipei Med Univ, Ctr Comprehens Canc, Taipei, Taiwan
[5] Taipei Med Univ, Shuang Ho Hosp, Dept Lab Med, Taipei, Taiwan
[6] Taipei Med Univ, Shuang Ho Hosp, Dept Med Res, Ctr Evidence Based Hlth Care, New Taipei, Taiwan
[7] Taipei Med Univ, Shuang Ho Hosp, Dept Internal Med, Div Endocrinol & Metab, New Taipei, Taiwan
[8] Taipei Med Univ, Coll Med, Sch Med, Dept Internal Med, Taipei, Taiwan
[9] Lake Erie Coll Osteopath Med, Bradenton, FL 34211 USA
[10] Taipei Med Univ, Shuang Ho Hosp, Dept Surg, Div Gen Surg, New Taipei, Taiwan
[11] Taipei Med Univ, Coll Med, Sch Med, Dept Surg, Taipei, Taiwan
[12] Taipei Med Univ, Cochrane Taiwan, Taipei, Taiwan
来源
PHARMACOTHERAPY | 2018年 / 38卷 / 05期
关键词
Graves' orbitopathy; Graves' ophthalmopathy; thyroid eye disease; glucocorticoids; rituximab; CELL-TARGETED THERAPY; OPHTHALMOPATHY; DEPLETION; MODERATE;
D O I
10.1002/phar.2111
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Study ObjectiveTo investigate the efficacy and safety of rituximab in patients with Graves' orbitopathy (GO). DesignSystematic review and meta-analysis of four randomized controlled trials. PatientsA total of 293 patients with GO who received rituximab or control (either glucocorticoids, the established first-line therapy [three trials], or saline [one trial]). Measurements and ResultsRelevant studies published before February 2018 were identified from the PubMed, EMBASE, Cochrane Library, and Scopus databases and the ClinicalTrials.gov registry. Individual effect sizes were standardized, and a meta-analysis was conducted to calculate the pooled effect size by using a random-effects model. Treatment efficacy was assessed by measuring the following outcomes: clinical activity score (CAS), sight visual acuity reduction (NOSPECS) score, proptosis, diplopia, changes in eye volume, quality of life, and adverse events. In the four included trials, 113 patients in the rituximab group and 108 patients in the control group were evaluated. Compared with the control group, CAS (weighted mean difference 0.57, 95% confidence interval 0.25-0.89) was significantly reduced at 24weeks in the rituximab group. Compared with the control group, considerable proptosis reduction was also observed in the rituximab group; however, the difference was not significant. The proportion of adverse events in the rituximab group was not significantly higher than that in the glucocorticoid control group, but one of the included trials indicated that the rituximab group had more serious adverse events than the saline control group. ConclusionRituximab is a relatively safe and viable treatment that is superior to glucocorticoids or saline for patients with moderate to severe GO. However, the incidence of serious adverse events was disparate among the included trials. Additional studies involving a larger sample size and investigating the optimal rituximab dosage, frequency, and method of administration are warranted.
引用
收藏
页码:503 / 510
页数:8
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