首页> 美国卫生研究院文献>EBioMedicine >Calprotectin and the Magnitude of Antibodies to Infliximab in Clinically-stable Ulcerative Colitis Patients are More Relevant Than Infliximab Trough Levels and Pharmacokinetics for Therapeutic Escalation
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Calprotectin and the Magnitude of Antibodies to Infliximab in Clinically-stable Ulcerative Colitis Patients are More Relevant Than Infliximab Trough Levels and Pharmacokinetics for Therapeutic Escalation

机译:钙卫蛋白和临床稳定的溃疡性结肠炎患者中英夫利昔单抗抗体的数量比英夫利昔单糖谷水平和药物代谢动力学的治疗意义更大

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摘要

Although infliximab (IFX) is an efficient therapy for ulcerative colitis (UC) patients, a considerably high rate of therapeutic failures still occurs. This study aimed at a better understanding of IFX pharmacokinetics and pharmacodynamics among clinically-asymptomatic UC patients. This was a multicentric and prospective study involving 65 UC patients in the maintenance phase of IFX therapy. There were no significant differences between patients with positive and negative clinical, endoscopic and histological outcomes concerning their IFX trough levels (TLs), area under the IFX concentration vs. time curve (AUC), clearance and antibodies to infliximab (ATI) levels. However, the need to undergo therapeutic escalation later in disease development was significantly associated with higher ATI levels (2.62 μg/mL vs. 1.15 μg/mL, p = 0.028). Moreover, and after adjusting for disease severity, the HR (hazard ratio) for therapeutic escalation was significantly decreased for patients with an ATI concentration below 3 μg/mL (HR = 0.119, p = 0.010), and increased for patients with fecal calprotectin (FC) level above 250 μg/g (HR = 9.309, p = 0.018). In clinically-stable UC patients, IFX pharmacokinetic features cannot predict therapeutic response on a short-term basis. However, high levels of ATIs or FC may be indicative of a future therapeutic escalation.
机译:尽管英夫利昔单抗(IFX)对于溃疡性结肠炎(UC)患者是一种有效的治疗方法,但仍然有相当高的治疗失败率。这项研究旨在更好地了解临床无症状UC患者中的IFX药代动力学和药效学。这是一项多中心前瞻性研究,涉及IFX治疗维持阶段的65名UC患者。临床,内镜和组织学结果阳性和阴性的患者在其IFX谷水平(TLs),IFX浓度与时间曲线下的面积(AUC),清除率和英夫利昔单抗(ATI)水平之间均无显着差异。但是,疾病发展后期需要进行治疗升级与ATI较高水平显着相关(2.62μg/ mL与1.15μg/ mL,p = 0.028)。此外,在调整疾病严重程度后,对于ATI浓度低于3μg/ mL的患者(HR = 0.119,p = 0.010),用于治疗升级的HR(危险比)显着降低,而粪钙卫蛋白( FC)含量超过250μg/ g(HR = 9.309,p = 0.018)。在临床稳定的UC患者中,IFX的药代动力学特征无法短期预测治疗反应。但是,高水平的ATI或FC可能表明未来的治疗升级。

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