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Risk of malignancy including non-melanoma skin cancers with anti-tumour necrosis factor therapy in patients with rheumatoid arthritis: Meta-analysis of registries and systematic review of long-term extension studies

机译:类风湿关节炎患者使用抗肿瘤坏死因子治疗的包括非黑素瘤皮肤癌在内的恶性肿瘤风险:登记资料的荟萃分析和长期延伸研究的系统评价

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Objective: To assess the risk of malignancy in patients with rheumatoid arthritis (RA) receiving tumour necrosis factor (TNF) antagonists through a meta-analysis of data from registry studies and systematic review of long-term extension (LTE) studies. Methods: We systematically reviewed the literature up to January 2010 in the Embase and Medline databases, as well as abstracts from the 2008 and 2009 annual meetings of the EULAR and the ACR. The Mantel-Haenszel method was used to provide a common odds ratio (OR). Statistical heterogeneity was assessed by the chi-square Q test (%2). Standardised incidence ratio (SIR) was extracted for post-marketing studies and registries. Results: The literature search identified 634 articles and 110 abstracts, of which 12 and 5, respectively, were selected for analysis. We could perform a meta-analysis of data from 4 and 3 registries for risk of total malignancy and non-melanoma skin cancers (NMSC), respectively. The pooled OR for total malignancy and for NMSC was 0.81 [95% confidence interval (CI) 0.71-0.94] and 0.79 [0.62-1.02] in TNF antagonist group versus DMARD group, respectively. There was no significant heterogeneity. Among 4 LTE studies and 4 registries, no significant increase in the incidence of total malignancy was noted versus the general population. The only signal may be an increased risk of non-melanoma skin cancers. Conclusion: Our meta-analysis of data from registries and systematic review of LTE studies did not reveal an increased risk of total malignancy in RA patients receiving anti-TNF therapy.
机译:目的:通过对登记研究和长期延伸研究(LTE)研究的数据进行荟萃分析,评估接受肿瘤坏死因子(TNF)拮抗剂的类风湿关节炎(RA)患者的恶性风险。方法:我们系统地回顾了Embase和Medline数据库中截至2010年1月的文献以及EULAR和ACR的2008年和2009年年会的摘要。使用Mantel-Haenszel方法来提供公共比值比(OR)。统计异质性通过卡方Q检验(%2)进行评估。提取了标准化的发病率(SIR),用于上市后研究和注册。结果:文献检索确定了634篇文章和110篇摘要,分别选择了12篇和5篇进行分析。我们可以分别对来自4个和3个注册中心的数据进行荟萃分析,以分别评估总的恶性肿瘤和非黑色素瘤皮肤癌(NMSC)的风险。在TNF拮抗剂组与DMARD组中,总恶性肿瘤和NMSC的合并OR分别为0.81 [95%置信区间(CI)0.71-0.94]和0.79 [0.62-1.02]。没有明显的异质性。在4个LTE研究和4个注册中心中,与一般人群相比,总恶性肿瘤的发生率没有显着增加。唯一的信号可能是非黑素瘤皮肤癌风险增加。结论:我们对来自注册表的数据进行的荟萃分析以及对LTE研究的系统评价并未发现接受抗TNF治疗的RA患者的总恶性风险增加。

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