SERENE ER Analysis Part 2 SERENE-UC: Exposure-response Analysis of Higher Versus Standard Adalimumab Dosing Regimens for Patients with Moderately to Severely Active Ulcerative Colitis

IF 1.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Sven Stodtmann, Mong-Jen Chen, Ana Victoria Ponce-Bobadilla, Tricia K. Finney-Hayward, Jasmina Kalabic, Nael M. Mostafa
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Abstract

SERENE UC (NCT02065622) evaluated whether a higher adalimumab induction regimen improved patients with ulcerative colitis (UC) response, but a flat dose-response relationship was found in the induction study. We investigated exposure-response (ER) relationships in induction and maintenance studies considering patients’ baseline characteristics. Adalimumab exposures were simulated using the established population pharmacokinetic model. Multivariable logistic regressions were used to assess the efficacy endpoints (clinical remission, endoscopic remission, endoscopic improvement) at weeks 8 and 52. In the induction study, an increasing ER trend with heterogeneity between induction regimens was shown, suggesting average concentration (Cavg) had a significant impact on primary efficacy endpoints within each group. However, data were not described by a single ER curve. Using inverse effective clearance as the exposure metric described trends across induction regimens with a single curve. Patients with inherently lower effective adalimumab clearance responded better. The patient response rates at week 52 showed no heterogeneity. A short-term increase in adalimumab dose did not drive better responses for induction, and apparent ER relationships were better explained by patient-inherent lower clearance. Conversely, during maintenance up to week 52, increasing the concentration via dose translated to better responses more robustly. The ER findings for SERENE UC were consistent with SERENE CD.

SERENE ER 分析第 2 部分 SERENE-UC:针对中度至重度活动性溃疡性结肠炎患者的阿达木单抗高剂量与标准剂量方案的暴露-反应分析。
SERENE UC(NCT02065622)评估了较高的阿达木单抗诱导方案是否能改善溃疡性结肠炎(UC)患者的反应,但在诱导研究中发现剂量-反应关系平淡。考虑到患者的基线特征,我们调查了诱导和维持研究中的暴露-反应(ER)关系。我们使用已建立的群体药代动力学模型模拟了阿达木单抗的暴露量。使用多变量逻辑回归评估第8周和第52周的疗效终点(临床缓解、内镜缓解、内镜改善)。在诱导研究中,ER呈上升趋势,诱导方案之间存在异质性,表明平均浓度(Cavg)对各组的主要疗效终点有显著影响。然而,数据并不能用单一的ER曲线来描述。使用逆有效清除率作为暴露指标,可以用一条曲线描述不同诱导方案的趋势。阿达木单抗有效清除率较低的患者反应较好。第52周时的患者反应率没有显示出异质性。阿达木单抗剂量的短期增加并不能改善诱导治疗的反应,患者固有的较低清除率更能解释明显的ER关系。相反,在第52周之前的维持治疗期间,通过剂量增加阿达木单抗浓度能更有效地改善反应。SERENE UC的ER结果与SERENE CD一致。
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来源期刊
CiteScore
3.70
自引率
10.00%
发文量
154
期刊介绍: Clinical Pharmacology in Drug Development is an international, peer-reviewed, online publication focused on publishing high-quality clinical pharmacology studies in drug development which are primarily (but not exclusively) performed in early development phases in healthy subjects.
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