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生物制剂(包括乌司奴单抗)治疗难治性大动脉炎患者的长期结局。

Long-term outcomes of refractory Takayasu arteritis patients treated with biologics including ustekinumab.

机构信息

Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Ijinkai Takeda General Hospital, Kyoto, Japan.

出版信息

Mod Rheumatol. 2021 May;31(3):678-683. doi: 10.1080/14397595.2020.1800560. Epub 2020 Aug 19.

Abstract

OBJECTIVES

Biologics have been used to treat refractory Takayasu arteritis (TAK), but their efficacy and safety have not been sufficiently evaluated.

METHODS

We extracted clinical information from medical records for TAK patients who were treated with biologics including ustekinumab (UST) at Kyoto University Hospital. We also analysed the patient's genetic backgrounds.

RESULTS

Of 163 cases, 12 (7.4%) were treated with infliximab, tocilizumab, or UST (n = 3). Erythrocyte sedimentation rate (ESR), C-reactive protein levels (CRP), and prednisolone (PSL) dose were significantly decreased 12 months after the initiation of biologics. When compared with the 15 patients who were only treated with immunosuppressants (IS group), the change in ESR from baseline was significantly lower in the biologics group than in the IS group (-2 mm/h,  = .005). The proportion of patients with HLA-B*52 and the risk-type alleles of the SNP were similar in both groups. Among the biologics, TCZ showed the highest continuation rate. UST exhibited marginal effects on reducing ESR, CRP levels, and PSL dose. No adverse events were observed in patients with UST for approximately 3 years.

CONCLUSIONS

Biological treatments resulted in a reduction in inflammatory markers and PSL dose in refractory TAK patients.

摘要

目的

生物制剂已被用于治疗难治性 Takayasu 动脉炎(TAK),但其疗效和安全性尚未得到充分评估。

方法

我们从京都大学医院接受生物制剂治疗的 TAK 患者的病历中提取了临床信息。我们还分析了患者的遗传背景。

结果

在 163 例患者中,有 12 例(7.4%)接受了英夫利昔单抗、托珠单抗或乌司奴单抗(UST)治疗(n=3)。生物制剂治疗 12 个月后,红细胞沉降率(ESR)、C 反应蛋白(CRP)水平和泼尼松龙(PSL)剂量均显著降低。与仅接受免疫抑制剂(IS 组)治疗的 15 例患者相比,生物制剂组 ESR 从基线的变化明显低于 IS 组(-2mm/h,=0.005)。两组患者的 HLA-B*52 比例和 SNP 风险等位基因相似。在生物制剂中,TCZ 的续贯率最高。UST 对降低 ESR、CRP 水平和 PSL 剂量有一定作用。接受 UST 治疗约 3 年的患者未出现不良事件。

结论

生物治疗可降低难治性 TAK 患者的炎症标志物和 PSL 剂量。

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