Department of Biomedicine, Unity of Pharmacology and Therapeutics, Faculty of Medicine, University of Porto, Porto, Portugal; MedInUP, Centre for Drug Discovery and Innovative Medicines, University of Porto, 4200 Porto, Portugal; Gastroenterology Department, Centro Hospitalar São João, Porto, Portugal.
MedInUP, Centre for Drug Discovery and Innovative Medicines, University of Porto, 4200 Porto, Portugal.
EBioMedicine. 2017 Jul;21:123-130. doi: 10.1016/j.ebiom.2017.06.004. Epub 2017 Jun 7.
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 (2.62μg/mL vs. 1.15μg/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 3μg/mL (HR=0.119, p=0.010), and increased for patients with fecal calprotectin (FC) level above 250μg/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.
虽然英夫利昔单抗(IFX)是治疗溃疡性结肠炎(UC)患者的有效疗法,但仍有相当高的治疗失败率。本研究旨在更好地了解临床无症状 UC 患者的 IFX 药代动力学和药效动力学。这是一项多中心前瞻性研究,涉及 65 例接受 IFX 维持治疗的 UC 患者。在 IFX 谷浓度(TLs)、IFX 浓度-时间曲线下面积(AUC)、清除率和抗英夫利昔单抗抗体(ATI)水平方面,临床、内镜和组织学结果阳性和阴性的患者之间没有显著差异。然而,在疾病进展过程中需要进行治疗升级的患者,其 ATI 水平显著较高(2.62μg/mL 与 1.15μg/mL,p=0.028)。此外,在调整疾病严重程度后,ATI 浓度低于 3μg/mL 的患者进行治疗升级的 HR(风险比)显著降低(HR=0.119,p=0.010),而粪便钙卫蛋白(FC)水平高于 250μg/g 的患者的 HR 显著升高(HR=9.309,p=0.018)。在临床稳定的 UC 患者中,IFX 药代动力学特征不能在短期内预测治疗反应。然而,高 ATI 或 FC 水平可能预示着未来需要进行治疗升级。