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在中重度银屑病患者中,临床应答与注射后 4 周的乌司奴单抗浓度相关。

Clinical response correlates with 4-week postinjection ustekinumab concentrations in patients with moderate-to-severe psoriasis.

机构信息

Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.

Department of Dermatology, Ghent University Hospital, Ghent, Belgium.

出版信息

Br J Dermatol. 2020 Feb;182(2):390-397. doi: 10.1111/bjd.18016. Epub 2019 Jul 24.

Abstract

BACKGROUND

Cost-effective use of biologicals is important. As drug concentrations have been linked to clinical outcomes, monitoring drug concentrations is a valuable tool to guide clinical decision-making. A concentration-response relationship for ustekinumab at trough is uncertain owing to the contradictory results reported.

OBJECTIVES

To investigate the relationship between 4-week postinjection ustekinumab concentrations and clinical response in patients with psoriasis.

METHODS

Forty-nine patients with moderate-to-severe psoriasis treated with 45 mg or 90 mg ustekinumab every 12 weeks for ≥ 16 weeks were included. Ustekinumab serum concentrations and anti-ustekinumab antibodies were measured at week 4 after injection and disease severity was assessed by Psoriasis Area and Severity Index (PASI).

RESULTS

At week 4 after injection, a significantly negative correlation was observed between ustekinumab concentrations and absolute PASI score up to 5·9 μg mL (ρ = -0·357, P = 0·032). Ustekinumab concentrations were higher in optimal responders (PASI ≤ 2) than in suboptimal responders (PASI > 2) (4·0 vs 2·8 μg mL , P = 0·036). The ustekinumab concentration threshold associated with optimal response was determined to be 3·6 μg mL (area under the curve 0·71, sensitivity 86%, specificity 63%). Only one patient (2%) had anti-ustekinumab antibodies. Psoriatic arthritis was identified as an independent predictor of higher PASI scores and higher ustekinumab concentrations (P = 0·003 and P = 0·048, respectively).

CONCLUSIONS

A concentration-response relationship at week 4 after injection was observed for patients with psoriasis treated with ustekinumab. Monitoring 4-week postinjection ustekinumab concentrations could timely identify underexposed patients who might benefit from treatment optimization. What's already known about this topic? Monitoring drug concentrations is a valuable tool that can guide clinical decision-making when drug concentrations are linked to clinical outcomes. The presence of a concentration-response relationship for ustekinumab at trough is still debated owing to the contradictory results reported. What does this study add? A concentration-response relationship at week 4 after injection for ustekinumab-treated patients with psoriasis was demonstrated. Monitoring 4-week postinjection ustekinumab concentrations could timely identify underexposed patients who might benefit from treatment optimization. Based on the findings of this study, a treatment algorithm for patients with a suboptimal response is proposed.

摘要

背景

生物制剂的成本效益利用很重要。由于药物浓度与临床结局相关,因此监测药物浓度是指导临床决策的有价值工具。由于报告的结果相互矛盾,乌司奴单抗在谷浓度时的浓度-反应关系尚不确定。

目的

研究银屑病患者注射后 4 周乌司奴单抗浓度与临床反应之间的关系。

方法

纳入 49 例接受每 12 周 45mg 或 90mg 乌司奴单抗治疗至少 16 周的中重度银屑病患者。在注射后 4 周时测量乌司奴单抗血清浓度和抗乌司奴单抗抗体,并用银屑病面积和严重程度指数(PASI)评估疾病严重程度。

结果

注射后 4 周时,乌司奴单抗浓度与绝对 PASI 评分呈显著负相关(ρ=-0.357,P=0.032)。与非最佳应答者(PASI>2)相比,最佳应答者(PASI≤2)的乌司奴单抗浓度更高(4.0 比 2.8μg/mL,P=0.036)。确定最佳应答的乌司奴单抗浓度阈值为 3.6μg/mL(曲线下面积 0.71,敏感性 86%,特异性 63%)。只有 1 例患者(2%)有抗乌司奴单抗抗体。银屑病关节炎是 PASI 评分较高和乌司奴单抗浓度较高的独立预测因素(P=0.003 和 P=0.048)。

结论

在接受乌司奴单抗治疗的银屑病患者中,观察到注射后 4 周时的浓度-反应关系。监测注射后 4 周时的乌司奴单抗浓度可以及时识别出药物暴露不足的患者,这些患者可能受益于治疗优化。

本研究的其他发现

在接受乌司奴单抗治疗的银屑病患者中,在注射后 4 周时,观察到了浓度-反应关系。监测注射后 4 周时的乌司奴单抗浓度可以及时识别出药物暴露不足的患者,这些患者可能受益于治疗优化。基于本研究的结果,提出了一种针对治疗反应不佳患者的治疗算法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99de/7028119/964bb7bbaeb3/BJD-182-390-g001.jpg

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