Department of Gastroenterology and Hepatology, Leiden University Medical Centre, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
Division Gastroenterology-Hepatology, Maastricht University Medical Center+, Maastricht, The Netherlands.
Dig Dis Sci. 2023 Jun;68(6):2647-2657. doi: 10.1007/s10620-023-07822-7. Epub 2023 Mar 15.
It is unknown whether ustekinumab (UST) levels can predict clinical outcomes in Crohn's disease (CD) patients. We assessed the exposure-response relationship of UST trough concentrations with biochemical outcomes at week 24 in a prospective, real-world setting.
We performed a prospective study in patients with CD starting UST in four academic centres in the Netherlands. All patients received a weight-adjusted intravenous (IV) UST induction dose, followed by one subcutaneous (SC) dose of 90 mg UST at 8 weeks. Maintenance therapy consisted of 90 mg subcutaneous UST every 8 or 12 weeks. Individual UST concentration time course during treatment were estimated using a population pharmacokinetic (PK) model. Quartile analysis and logistic regression were performed to analyse if UST concentrations at week 8 were associated with biochemical remission rates at week 24 (C-reactive protein (CRP) ≤ 5 mg/L and / or faecal calprotectin (FC) ≤ 250 mg/kg).
In total, 124 patients with CD were included. Patients achieving biochemical remission at week 12 and 24 had significantly higher UST levels at week 8 compared to patients without biochemical remission (6.6 µg/mL versus 3.9 µg/mL, P < 0.01 and 6.3 µg/mL versus 3.9 µg/mL, P < 0.01, respectively). In quartile analysis, patients with UST levels in the highest quartile (≥ 6.3 µg/mL at week 8) had higher biochemical remission rates at week 12 and week 24. There was no association between UST levels at and corticosteroid-free clinical remission rates.
In this real-world cohort of patients with CD, UST levels in the highest quartile (≥ 6.3 µg/mL) at week 8 were associated with higher biochemical remission rates at week 24.
乌司奴单抗(UST)水平能否预测克罗恩病(CD)患者的临床结局尚不清楚。我们在荷兰的四个学术中心进行了一项前瞻性、真实世界研究,评估了 UST 谷浓度与第 24 周生化结局的暴露-反应关系。
我们对开始使用 UST 的 CD 患者进行了一项前瞻性研究,这些患者来自荷兰的四个学术中心。所有患者均接受了基于体重的静脉(IV)UST 诱导剂量,然后在第 8 周时接受 90mg 皮下(SC)UST 剂量。维持治疗包括每 8 或 12 周皮下给予 90mg UST。使用群体药代动力学(PK)模型估计治疗期间个体 UST 浓度时间曲线。进行四分位分析和逻辑回归,以分析第 8 周时的 UST 浓度是否与第 24 周的生化缓解率相关(C 反应蛋白(CRP)≤5mg/L 和/或粪便钙卫蛋白(FC)≤250mg/kg)。
共纳入 124 例 CD 患者。与生化缓解不良的患者相比,第 12 周和第 24 周生化缓解的患者在第 8 周时 UST 水平显著更高(6.6μg/mL 比 3.9μg/mL,P<0.01 和 6.3μg/mL 比 3.9μg/mL,P<0.01)。在四分位分析中,第 8 周 UST 水平处于最高四分位数(≥6.3μg/mL)的患者在第 12 周和第 24 周的生化缓解率更高。第 8 周时 UST 水平与无皮质类固醇的临床缓解率之间没有关联。
在这项 CD 真实世界队列研究中,第 8 周 UST 水平处于最高四分位数(≥6.3μg/mL)的患者在第 24 周时生化缓解率更高。