Department of Pharmaceutics, Center for Pharmacometrics and Systems Pharmacology, College of Pharmacy, University of Florida, Orlando, Florida, USA.
Department of Physical Therapy, University of Florida, Gainesville, Florida, USA.
CPT Pharmacometrics Syst Pharmacol. 2023 Oct;12(10):1437-1449. doi: 10.1002/psp4.13021. Epub 2023 Aug 27.
Although regulatory agencies encourage inclusion of imaging biomarkers in clinical trials for Duchenne muscular dystrophy (DMD), industry receives minimal guidance on how to use these biomarkers most beneficially in trials. This study aims to identify the optimal use of muscle fat fraction biomarkers in DMD clinical trials through a quantitative disease-drug-trial modeling and simulation approach. We simultaneously developed two multivariate models quantifying the longitudinal associations between 6-minute walk distance (6MWD) and fat fraction measures from vastus lateralis and soleus muscles. We leveraged the longitudinal individual-level data collected for 10 years through the ImagingDMD study. Age of the individuals at assessment was chosen as the time metric. After the longitudinal dynamic of each measure was modeled separately, the selected univariate models were combined using correlation parameters. Covariates, including baseline scores of the measures and steroid use, were assessed using the full model approach. The nonlinear mixed-effects modeling was performed in Monolix. The final models showed reasonable precision of the parameter estimates. Simulation-based diagnostics and fivefold cross-validation further showed the model's adequacy. The multivariate models will guide drug developers on using fat fraction assessment most efficiently using available data, including the widely used 6MWD. The models will provide valuable information about how individual characteristics alter disease trajectories. We will extend the multivariate models to incorporate trial design parameters and hypothetical drug effects to inform better clinical trial designs through simulation, which will facilitate the design of clinical trials that are both more inclusive and more conclusive using fat fraction biomarkers.
尽管监管机构鼓励在杜氏肌营养不良症 (DMD) 的临床试验中纳入成像生物标志物,但业界在如何最有效地将这些生物标志物用于试验方面几乎没有得到指导。本研究旨在通过定量疾病-药物-试验建模和模拟方法确定肌肉脂肪分数生物标志物在 DMD 临床试验中的最佳用途。我们同时开发了两个多变量模型,定量评估了股外侧肌和比目鱼肌的 6 分钟步行距离 (6MWD) 和脂肪分数测量值之间的纵向相关性。我们利用通过 ImagingDMD 研究在 10 年内收集的个体水平的纵向数据。评估时个体的年龄被选为时间指标。对每个指标的纵向动态分别建模后,使用相关参数将选定的单变量模型组合在一起。使用全模型方法评估协变量,包括测量值的基线评分和类固醇的使用情况。非线性混合效应模型在 Monolix 中进行。最终模型显示参数估计值具有合理的精度。基于模拟的诊断和五倍交叉验证进一步表明了模型的充分性。多变量模型将指导药物开发者使用脂肪分数评估,最有效地利用现有数据,包括广泛使用的 6MWD。这些模型将提供有关个体特征如何改变疾病轨迹的有价值信息。我们将扩展多变量模型以纳入试验设计参数和假设的药物效应,通过模拟为更好的临床试验设计提供信息,这将有助于使用脂肪分数生物标志物设计更具包容性和更具结论性的临床试验。