Translational Research in Gastrointestinal Disorders, Department of Chronic Disease and Metabolism, KU Leuven, Leuven, Belgium.
Laboratory of Morphology and Molecular Pathology, University Hospitals Leuven, Leuven, Belgium.
J Crohns Colitis. 2022 Nov 1;16(10):1562-1570. doi: 10.1093/ecco-jcc/jjac067.
Histo-endoscopic outcomes are being proposed as new treatment targets in ulcerative colitis [UC]. Little is known about the pharmacokinetic-pharmacodynnamic [PK-PD] relationship of ustekinumab [UST] in UC patients or whether serum UST concentrations reflect tissue drug exposure. We aimed to study UST serum concentrations and their relation to tissue exposure and drug effectiveness in a real-world setting.
A total of 42 UC patients starting UST were prospectively followed by clinical, endoscopic and histological assessments at Week 16. Histological remission was defined as Nancy Histology Index of 0. Analogous to the UNIFI programme, histo-endoscopic mucosal improvement was defined as a combination of histological improvement [Geboes ≤3.1] and endoscopic improvement [MES ≤1]. Paired trough serum samples and colonic mucosal biopsies were collected for UST levels measurement.
After 16 weeks [IQR 15.8-16.4] of therapy, histological remission and histo-endoscopic mucosal improvement were observed in 19 [45%] and 18 [43%] patients, respectively. Patients who achieved these outcomes had higher serum UST levels than those who did not. Patients with shorter disease duration and clinical response at Week 8 had higher odds to achieve histological remission. UST concentrations from paired serum and biopsy samples revealed a strong positive correlation [r = 0.88, p < 0.001], in both inflamed and uninflamed tissue.
In this real-world cohort of refractory UC patients initiating UST, more than a third of the patients achieved histological remission. A drug exposure-response relationship was observed for histo-endoscopic outcomes, with no added value of measuring tissue exposure given the strong correlation with serum exposure.
组织学内镜结果被认为是溃疡性结肠炎[UC]的新治疗目标。关于 UC 患者乌司奴单抗[UST]的药代动力学-药效学[PK-PD]关系知之甚少,也不知道血清 UST 浓度是否反映组织药物暴露情况。我们旨在研究真实环境中 UST 血清浓度及其与组织暴露和药物疗效的关系。
总共 42 名开始使用 UST 的 UC 患者前瞻性地进行了临床、内镜和组织学评估,时间为 16 周。组织学缓解定义为 Nancy 组织学指数为 0。类似于 UNIFI 项目,组织学内镜黏膜改善定义为组织学改善[Geboes≤3.1]和内镜改善[MES≤1]的组合。采集配对的血清样本和结肠黏膜活检标本,用于 UST 水平的测量。
经过 16 周[IQR 15.8-16.4]的治疗,19 名[45%]和 18 名[43%]患者分别达到了组织学缓解和组织学内镜黏膜改善。达到这些结果的患者血清 UST 水平高于未达到的患者。在第 8 周具有较短疾病病程和临床反应的患者,有更高的机会达到组织学缓解。来自配对血清和活检样本的 UST 浓度显示出强烈的正相关[r=0.88,p<0.001],在炎症和非炎症组织中均如此。
在本研究中,难治性 UC 患者开始使用 UST,超过三分之一的患者达到了组织学缓解。观察到组织学内镜结果的药物暴露反应关系,鉴于血清暴露与组织暴露之间的强相关性,测量组织暴露没有额外的价值。