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比较治疗多关节型病程幼年特发性关节炎患者的第二种肿瘤坏死因子抑制剂与非肿瘤坏死因子生物制剂的疗效。

Comparative Effectiveness of a Second Tumor Necrosis Factor Inhibitor Versus a Non-Tumor Necrosis Factor Biologic in the Treatment of Patients With Polyarticular-Course Juvenile Idiopathic Arthritis.

机构信息

University of Alabama at Birmingham.

Childhood Arthritis and Rheumatology Research Alliance, Washington, DC.

出版信息

Arthritis Care Res (Hoboken). 2024 Aug;76(8):1090-1098. doi: 10.1002/acr.25339. Epub 2024 May 7.

Abstract

OBJECTIVE

The objective of this study was to compare the effectiveness of a second tumor necrosis factor inhibitor (TNFi) versus a non-TNFi biologic following discontinuation of a TNFi for patients with polyarticular-course juvenile idiopathic arthritis (pJIA).

METHODS

Using the Childhood Arthritis and Rheumatology Research Alliance Registry, patients with pJIA who started receiving a second biologic following a first TNFi were identified. Patients were required to have no active uveitis on the index date and a visit six months after the index date. Outcome measures included Clinical Juvenile Arthritis Disease Activity Score with a maximum of 10 active joints (cJADAS10), cJADAS10 inactive disease (ID; ≤2.5) and cJADAS10 minimal disease activity (MiDA; ≤5). Multiple imputation was used to account for missing data. Adjusted odds ratios (aORs) were calculated using propensity score quintiles to compare outcomes at six months following second biologic initiation.

RESULTS

There were 216 patients included, 84% initially received etanercept, and most patients stopped receiving it because of its ineffectiveness (74%). A total of 183 (85%) started receiving a second TNFi, and 33 (15%) started receiving a non-TNFi. Adalimumab was the most common second biologic received (71% overall, 84% of second TNFi), and tocilizumab was the most common non-TNFi second biologic received (9% overall, 58% of non-TNFi). There was no difference between receiving TNFi versus non-TNFi in cJADAS10 ID (29% vs 25%; aOR 1.23, 95% confidence interval [CI] 0.47-3.20) or at least MiDA (43% vs 39%; aOR 1.11, 95% CI 0.47-2.62) at six months.

CONCLUSION

Most patients with pJIA started receiving TNFi rather than non-TNFi as their second biologic, and there were no differences in disease activity at six months.

摘要

目的

本研究旨在比较多关节型幼年特发性关节炎(pJIA)患者停用肿瘤坏死因子抑制剂(TNFi)后,使用第二种 TNFi 与非 TNFi 生物制剂的疗效。

方法

本研究使用儿童关节炎和风湿病研究联盟(CARRA)登记处,确定了在开始使用第二种生物制剂后接受第一种 TNFi 的 pJIA 患者。患者需在索引日期无活动性葡萄膜炎,且在索引日期后六个月有一次就诊。结局指标包括最大 10 个活跃关节的临床幼年特发性关节炎疾病活动评分(cJADAS10)、cJADAS10 无疾病活动(ID;≤2.5)和 cJADAS10 微小疾病活动(MiDA;≤5)。采用多重插补法处理缺失数据。使用倾向评分五分位数计算调整后比值比(aOR),以比较第二种生物制剂起始后六个月的结局。

结果

共纳入 216 例患者,84%患者最初接受依那西普治疗,大多数患者因无效(74%)而停止使用该药。共有 183 例(85%)患者开始接受第二种 TNFi,33 例(15%)患者开始接受非 TNFi。阿达木单抗是最常用的第二种生物制剂(总体 71%,第二种 TNFi 中 84%),托珠单抗是最常用的非 TNFi 第二种生物制剂(总体 9%,非 TNFi 中 58%)。在 cJADAS10 ID(29%比 25%;aOR 1.23,95%置信区间 [CI] 0.47-3.20)或至少 MiDA(43%比 39%;aOR 1.11,95% CI 0.47-2.62)方面,接受 TNFi 与非 TNFi 之间没有差异。

结论

大多数 pJIA 患者开始接受 TNFi 作为他们的第二种生物制剂,而非非 TNFi,并且在六个月时疾病活动没有差异。

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