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英夫利昔单抗作为类风湿关节炎一线治疗的长期疗效和成本效益:系统评价和荟萃分析。

Long-term efficacy and cost-effectiveness of infliximab as first-line treatment in rheumatoid arthritis: systematic review and meta-analysis.

机构信息

Department of Health Economics, Corvinus University of Budapest , Budapest , Hungary.

Doctoral School of Business and Management, Corvinus University of Budapest , Budapest , Hungary.

出版信息

Expert Rev Pharmacoecon Outcomes Res. 2019 Oct;19(5):537-549. doi: 10.1080/14737167.2019.1647104. Epub 2019 Aug 1.

Abstract

: Early biological treatment of rheumatoid arthritis (RA) may reverse the autoimmune response in some patients resulting in favorable long-term outcomes. Although the cost-effectiveness of this strategy has been questioned, biosimilar entries warrant the revision of clinical and pharmaco-economic evidence. : We conducted a systematic review of randomized controlled trials (RCTs) published up to 24 May 2018 in Pubmed, EMBASE and Cochrane CENTRAL, comparing infliximab with non-biological therapy in patients with RA naïve to methotrexate. We performed meta-analyses for efficacy outcomes at month 6 and years 1 and 2. Six RCTs were identified, involving 1832 patients. At month 6 ACR70 response and remission, and at year 1 ACR20/ACR70 responses and remission were improved significantly with first-line infliximab versus control. The differences were not significant at year 2. We reviewed cost-utility studies, up to 31 October 2018 in PubMed, Cochrane CENTRAL and the CRD HTA databases. Four studies indicated that first-line use of originator infliximab calculated at 2005-2008 prices was not cost-effective. : We demonstrated the efficacy benefits of first-line infliximab therapy up to 1 year in methotrexate-naïve RA. We highlighted the need for standardized reporting of outcomes and conducting cost-effectiveness analyses of first-line biosimilar therapy in RA.

摘要

早期类风湿关节炎(RA)的生物治疗可能会使一些患者的自身免疫反应逆转,从而产生有利的长期结果。尽管这种策略的成本效益受到质疑,但生物类似药的出现需要对临床和药物经济学证据进行修订。

我们对截至 2018 年 5 月 24 日在 Pubmed、EMBASE 和 Cochrane CENTRAL 上发表的随机对照试验(RCTs)进行了系统评价,比较了甲氨蝶呤初治的 RA 患者中使用英夫利昔单抗与非生物疗法的疗效。我们对第 6 个月和第 1 年和第 2 年的疗效结果进行了荟萃分析。共确定了 6 项 RCT,涉及 1832 名患者。在第 6 个月时,ACR70 缓解和缓解率,以及在第 1 年时 ACR20/ACR70 缓解率和缓解率均明显优于一线英夫利昔单抗与对照组。在第 2 年时,差异无统计学意义。我们在 PubMed、Cochrane CENTRAL 和 CRD HTA 数据库中检索了截至 2018 年 10 月 31 日的成本效用研究。四项研究表明,以 2005-2008 年的价格计算,一线使用原研英夫利昔单抗是不具有成本效益的。

我们证明了在甲氨蝶呤初治的 RA 中,一线英夫利昔单抗治疗在 1 年内具有疗效优势。我们强调需要标准化报告结果,并对 RA 一线生物类似药治疗进行成本效益分析。

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