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早期 vedolizumab 谷浓度可预测炎症性肠病患者第一年的治疗持续时间。

Early vedolizumab trough levels predict treatment persistence over the first year in inflammatory bowel disease.

机构信息

UOC Medicina Interna e Gastroenterologia Columbus, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Università Cattolica del Sacro Cuore, Rome, Italy.

出版信息

United European Gastroenterol J. 2019 Nov;7(9):1189-1197. doi: 10.1177/2050640619873784. Epub 2019 Sep 3.

Abstract

BACKGROUND

Data from trials of vedolizumab for inflammatory bowel disease and from real-world studies suggest an exposure-response relationship, such that vedolizumab trough levels may predict clinical and endoscopic outcomes.

OBJECTIVE

The purpose of this study was to evaluate in a prospective observational study the utility of an early vedolizumab trough level assay for predicting the first-year vedolizumab therapy outcome.

METHODS

This prospective observational study included consecutive inflammatory bowel disease patients. We measured vedolizumab trough levels and anti-vedolizumab antibodies at weeks 6 and 14. Clinical outcome was assessed at weeks 6, 14, 22 and 54. The primary endpoint was the correlation between early vedolizumab trough levels and vedolizumab persistence over the first year of treatment, defined as the maintenance of vedolizumab therapy due to sustained clinical benefit.

RESULTS

We included 101 patients initiating vedolizumab. A cut-off vedolizumab trough level of 16.55 µg/ml at week 14 predicted vedolizumab persistence within the first year of therapy, with 73.3% sensitivity and 59.4% specificity ( = 0.0009). Week 14 vedolizumab trough level was significantly higher in patients with clinical remission at weeks 14, 22 and 54; and in patients achieving mucosal healing within 54 weeks.

CONCLUSION

High vedolizumab trough level at week 14 was associated with a higher probability of maintaining vedolizumab therapy over the first year due to sustained clinical benefit.

摘要

背景

来自于 vedolizumab 治疗炎症性肠病的临床试验和真实世界研究的数据表明,存在暴露-反应关系,即 vedolizumab 谷浓度可能预测临床和内镜结局。

目的

本研究旨在通过前瞻性观察性研究,评估 vedolizumab 早期谷浓度检测在预测 vedolizumab 治疗第一年结局中的作用。

方法

本前瞻性观察性研究纳入了连续的炎症性肠病患者。我们在第 6 周和第 14 周检测了 vedolizumab 谷浓度和抗 vedolizumab 抗体。在第 6 周、第 14 周、第 22 周和第 54 周评估临床结局。主要终点是 vedolizumab 早期谷浓度与第一年 vedolizumab 治疗持续性之间的相关性,治疗持续性定义为由于持续的临床获益而维持 vedolizumab 治疗。

结果

我们纳入了 101 例开始使用 vedolizumab 的患者。第 14 周时 vedolizumab 谷浓度的截断值为 16.55 µg/ml,预测了第一年治疗中的 vedolizumab 持续性,敏感性为 73.3%,特异性为 59.4%( = 0.0009)。第 14 周时临床缓解的患者、第 14 周、第 22 周和第 54 周时临床缓解的患者、第 54 周时实现黏膜愈合的患者,其 vedolizumab 谷浓度显著更高。

结论

第 14 周时 vedolizumab 谷浓度较高与由于持续的临床获益而更有可能在第一年维持 vedolizumab 治疗相关。

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