Minichmayr I K, Dreesen E, Centanni M, Wang Z, Hoffert Y, Friberg L E, Wicha S G
Dept. of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
Clinical Pharmacology and Pharmacotherapy Unit, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
Adv Drug Deliv Rev. 2024 Dec;215:115421. doi: 10.1016/j.addr.2024.115421. Epub 2024 Aug 17.
Model-informed precision dosing (MIPD) stands as a significant development in personalized medicine to tailor drug dosing to individual patient characteristics. MIPD moves beyond traditional therapeutic drug monitoring (TDM) by integrating mathematical predictions of dosing and considering patient-specific factors (patient characteristics, drug measurements) as well as different sources of variability. For this purpose, rigorous model qualification is required for the application of MIPD in patients. This review delves into new methods in model selection and validation, also highlighting the role of machine learning in improving MIPD, the utilization of biosensors for real-time monitoring, as well as the potential of models integrating biomarkers for efficacy or toxicity for precision dosing. The clinical evidence of TDM and MIPD is discussed for various medical fields including infection medicine, oncology, transplant medicine, and inflammatory bowel diseases, thereby underscoring the role of pharmacokinetics/pharmacodynamics and specific biomarkers. Further research, particularly randomized clinical trials, is warranted to corroborate the value of MIPD in enhancing patient outcomes and advancing personalized medicine.
模型引导的精准给药(MIPD)是个性化医疗领域的一项重大进展,旨在根据个体患者特征调整药物剂量。MIPD超越了传统的治疗药物监测(TDM),它整合了剂量的数学预测,并考虑了患者特定因素(患者特征、药物测量值)以及不同的变异来源。为此,MIPD在患者中的应用需要严格的模型验证。本综述深入探讨了模型选择和验证的新方法,还强调了机器学习在改进MIPD中的作用、生物传感器用于实时监测的应用,以及整合生物标志物以实现疗效或毒性精准给药的模型的潜力。讨论了TDM和MIPD在包括感染医学、肿瘤学、移植医学和炎症性肠病在内的各个医学领域的临床证据,从而强调了药代动力学/药效学和特定生物标志物的作用。有必要进行进一步的研究,尤其是随机临床试验,以证实MIPD在改善患者预后和推进个性化医疗方面的价值。