JCC:维持治疗期间较高的Vedolizumab谷浓度与炎症性肠病的无皮质类固醇缓解相关

2019-08-18 不详 MedSci原创

Vedolizumab是一种抗-α4β7生物制剂,目前已被批准用于治疗溃疡性结肠炎[UC]和克罗恩病[CD]。本项研究的目的是探究维多珠单抗浓度与炎症性肠病患者无激素缓解期的关系。

背景和目的
Vedolizumab是一种抗-α4β7生物制剂,目前已被批准用于治疗溃疡性结肠炎[UC]和克罗恩病[CD]。本项研究的目的是探究维多珠单抗浓度与炎症性肠病患者无激素缓解期的关系。

方法
研究人员对使用维多珠单抗治疗的炎症性肠病[IBD]患者进行了横断面多中心研究。均相迁移率变动分析[HMSA]用于确定维多珠单抗和抗药物抗体[ATVs]的血清浓度。主要观察结果是无皮质类固醇的临床缓解时间、C-反应蛋白[CRP]水平。次要结果包括无皮质类固醇内镜下缓解和粘膜深度缓解。

结果
本项研究总共纳入258名IBD患者[55%CD和45%UC]。临床和生化缓解期患者的维多珠单抗浓度显着较高[12.7μg/ mL vs10.1μg/ mL,p = 0.002]。内镜和深度缓解患者的浓度也较高[14.2μg/ mL vs 8.5μg/ mL,p = 0.003和14.8μg/ mL vs10.1μg/ mL,p = 0.01]。在控制潜在的混杂因素后,维多珠单抗浓度>11.5μg/ mL的IBD患者获得无皮质类固醇临床和生化缓解是低于11.5μg/ mL 的2.4倍。

结论
本项研究发现维持治疗期间较高的Vedolizumab谷浓度与炎症性肠病的长期无皮质类固醇缓解相关。

原始出处:

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    2020-05-13 snf701207
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    2020-02-22 jyzxjiangqin

    维持治疗新疗法!。

    0

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