Translational Informatics, TMED, Sanofi, Bridgewater, New Jersey, USA.
Sanofi Genzyme, Cambridge, Massachusetts, USA.
CPT Pharmacometrics Syst Pharmacol. 2018 Jul;7(7):442-452. doi: 10.1002/psp4.12304. Epub 2018 Jun 19.
Acid sphingomyelinase deficiency (ASMD) is a rare lysosomal storage disorder with heterogeneous clinical manifestations, including hepatosplenomegaly and infiltrative pulmonary disease, and is associated with significant morbidity and mortality. Olipudase alfa (recombinant human acid sphingomyelinase) is an enzyme replacement therapy under development for the non-neurological manifestations of ASMD. We present a quantitative systems pharmacology (QSP) model supporting the clinical development of olipudase alfa. The model is multiscale and mechanistic, linking the enzymatic deficiency driving the disease to molecular-level, cellular-level, and organ-level effects. Model development was informed by natural history, and preclinical and clinical studies. By considering patient-specific pharmacokinetic (PK) profiles and indicators of disease severity, the model describes pharmacodynamic (PD) and clinical end points for individual patients. The ASMD QSP model provides a platform for quantitatively assessing systemic pharmacological effects in adult and pediatric patients, and explaining variability within and across these patient populations, thereby supporting the extrapolation of treatment response from adults to pediatrics.
酸性鞘磷脂酶缺乏症 (ASMD) 是一种罕见的溶酶体贮积症,具有异质性的临床表现,包括肝脾肿大和浸润性肺疾病,并与较高的发病率和死亡率相关。Olipudase alfa(重组人酸性鞘磷脂酶)是一种正在开发的用于治疗 ASMD 非神经表现的酶替代疗法。我们提出了一个支持olipudase alfa 临床开发的定量系统药理学 (QSP) 模型。该模型是多尺度和机制性的,将导致疾病的酶缺乏与分子水平、细胞水平和器官水平的效应联系起来。模型的开发得到了自然史、临床前和临床研究的信息支持。通过考虑患者特定的药代动力学 (PK) 特征和疾病严重程度的指标,该模型描述了个体患者的药效学 (PD) 和临床终点。ASMD 的 QSP 模型为定量评估成人和儿科患者的系统药理学效应提供了一个平台,并解释了这些患者群体内和群体间的可变性,从而支持从成人到儿科的治疗反应外推。