Ustekinumab与其他生物制剂治疗中重度斑块性银屑病的比较:贝叶斯网络荟萃分析

Vincent W Lin, Sarah Ringold, Emily Beth Devine
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引用次数: 7

摘要

目的通过银屑病面积和严重程度指数(PASI)比较ustekinumab与其他生物制剂在中重度斑块型银屑病成人患者中的疗效。我们使用MEDLINE (PubMed)、Embase、Cochrane图书馆和clinicaltrials.gov对1992年1月31日至2012年2月1日这段时间进行了系统检索。研究选择我们纳入了随机对照试验,将生物制剂与安慰剂或其他生物制剂在中度至重度斑块性银屑病患者中使用PASI进行比较。数据提取研究数据由我们两人独立提取,分歧以共识解决。提取的数据包括试验的规模、随访期、患者年龄范围、病程、体表面积累及、基线PASI、PASI反应和既往生物制剂治疗。采用贝叶斯网络进行meta分析,拟合3个回归模型:固定效应模型、随机效应模型和带元回归系数的随机效应模型。随机效应模型对这些数据的拟合效果最好。在两两比较中,与使用阿达木单抗相比,使用乌斯特金单抗与实现PASI减少75%的统计学上显著更高的几率相关(优势比[OR], 1.84;95%可信区间[CrI], 1.01-3.54),阿facept使用(OR, 10.38;CrI, 3.44-27.62)和依那西普使用(OR, 2.07;95% CrI, 1.42-3.06),但与使用英夫利昔单抗相比,相关几率较低(OR, 0.36;95% CrI, 0.14-0.82)。在治疗组比较中,与安慰剂相比,白细胞介素-12/23抑制剂实现PASI减少75%的几率最高(OR, 69.48;95% CrI, 36.89-136.46),其次是肿瘤坏死因子抑制剂(OR, 42.22;95% CrI, 27.94-69.34)和t细胞抑制剂(OR, 5.63;95% CrI, 1.35-24.24)。结论对于中重度斑块型银屑病的治疗,ustekinumab可能比阿达木单抗、依那西普和阿法西普更有效,但不优于英夫利昔单抗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of Ustekinumab With Other Biological Agents for the Treatment of Moderate to Severe Plaque Psoriasis: A Bayesian Network Meta-analysis.

OBJECTIVE To compare the efficacy of ustekinumab with that of other biological agents using the Psoriasis Area and Severity Index (PASI) among adult patients with moderate to severe plaque psoriasis. DATA SOURCES We conducted a systematic search of the period January 31, 1992, to February 1, 2012, using MEDLINE (PubMed), Embase, the Cochrane Library, and clinicaltrials.gov. STUDY SELECTION We included randomized controlled trials of biological agents compared with placebo or other biological agents using the PASI in patients who had moderate to severe plaque psoriasis. DATA EXTRACTION Study data were extracted independently by 2 of us, with disagreement resolved by consensus. Data extracted included the size of the trial, follow-up period, age range of patients, disease duration, body surface area involvement, baseline PASI, PASI response, and previous treatment with biological agents. DATA SYNTHESIS A Bayesian network meta-analysis was performed by fitting 3 regression models: a fixed-effects model, a random-effects model, and a random-effects model with meta-regression coefficients. The random-effects model achieved the best fit for these data. In pairwise comparisons, ustekinumab use was associated with statistically significantly higher odds for achieving a 75% reduction in the PASI compared with adalimumab use (odds ratio [OR], 1.84; 95% credible interval [CrI], 1.01-3.54), alefacept use (OR, 10.38; CrI, 3.44-27.62), and etanercept use (OR, 2.07; 95% CrI, 1.42-3.06) but was associated with lower odds compared with infliximab use (OR, 0.36; 95% CrI, 0.14-0.82) . In the therapeutic class comparison, the interleukin-12/23 inhibitor had the highest odds for achieving a 75% reduction in the PASI compared with placebo (OR, 69.48; 95% CrI, 36.89-136.46), followed by tumor necrosis factor inhibitors (OR, 42.22; 95% CrI, 27.94-69.34) and the T-cell inhibitor (OR, 5.63; 95% CrI, 1.35-24.24). CONCLUSION For the treatment of moderate to severe plaque psoriasis, ustekinumab may be more efficacious than adalimumab, etanercept, and alefacept but not infliximab.

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来源期刊
Archives of dermatology
Archives of dermatology 医学-皮肤病学
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