Shim Jaehee V, Rehberg Markus, Wagenhuber Britta, van der Graaf Piet H, Chung Douglas W
Certara Applied BioSimulation, Sheffield, United Kingdom.
Sanofi R&D, Translational Disease Modeling, Frankfurt amMain, Germany.
Front Pharmacol. 2025 Feb 25;16:1479666. doi: 10.3389/fphar.2025.1479666. eCollection 2025.
Disease activity scores are efficacy endpoints in clinical trials of inflammatory bowel disease (IBD) therapies. Crohn's disease activity index (CDAI), Mayo endoscopic score (MES) and Mayo score are frequently used in clinical trials. They rely on either the physician's observation of the inflammatory state of the patient's gastrointestinal tissue alone or combined with the patient's subjective evaluation of general wellbeing. Given the importance of these scores in evaluating the efficacy of drug treatment and disease severity, there has been interest in developing a computational approach to reliably predict these scores. A promising approach is using mechanistic models such as quantitative systems pharmacology (QSP) which simulate the mechanisms of the disease and its modulation by the drug pharmacology. However, extending QSP model simulations to clinical score predictions has been challenging due to the limited availability of gut biopsy measurements and the subjective nature of some of the evaluation criteria for these scores that cannot be described using mechanistic relationships. In this perspective, we examine details of IBD disease activity scores and current progress in building predictive models for these scores (such as biomarkers for disease activity). Then, we propose a method to leverage simulated markers of inflammation from a QSP model to predict IBD clinical scores using a machine learning algorithm. We will demonstrate how this combined approach can be used to (1) explore mechanistic insights underlying clinical observations; and (2) simulate novel therapeutic strategies that could potentially improve clinical outcomes.
疾病活动评分是炎症性肠病(IBD)治疗临床试验中的疗效终点。克罗恩病活动指数(CDAI)、梅奥内镜评分(MES)和梅奥评分在临床试验中经常被使用。它们要么仅依赖于医生对患者胃肠道组织炎症状态的观察,要么结合患者对总体健康状况的主观评估。鉴于这些评分在评估药物治疗疗效和疾病严重程度方面的重要性,人们一直对开发一种计算方法来可靠地预测这些评分感兴趣。一种有前景的方法是使用诸如定量系统药理学(QSP)之类的机制模型,该模型模拟疾病机制及其受药物药理学的调节。然而,由于肠道活检测量的可用性有限以及这些评分的一些评估标准具有主观性,无法用机制关系来描述,因此将QSP模型模拟扩展到临床评分预测一直具有挑战性。从这个角度出发,我们研究了IBD疾病活动评分的细节以及构建这些评分预测模型(如疾病活动生物标志物)的当前进展。然后,我们提出一种方法,利用来自QSP模型的炎症模拟标志物,使用机器学习算法来预测IBD临床评分。我们将展示这种组合方法如何用于(1)探索临床观察背后的机制见解;以及(2)模拟可能改善临床结果的新型治疗策略。