College of Pharmacy, University of Kentucky, Lexington, Kentucky, USA.
Clin Transl Sci. 2019 Jul;12(4):343-349. doi: 10.1111/cts.12636. Epub 2019 Apr 20.
Chimeric antigen receptor T-cell (CART) therapy is a new and promising cancer therapy. However, severe toxicity due to cytokine release syndrome (CRS) in CART-treated patients highlighted the possible danger of this new therapy. Disease burden and CART doses are the potential factors associated with CRS but the detail relationships between these factors and the severity of the CRS remain largely unknown. In this study, the quantitative systems pharmacology (QSP) approach is used to quantify the complex relationships among CART doses, disease burden, and pro inflammatory cytokines in human subjects and to gain relevant insights into the determinant of clinical toxicity/efficacy in development of CART therapy. The expansion of CART and elimination of B cells are more highly correlated with disease burden than the administered CART doses. To our best knowledge, this is the first QSP model that can describe the observed clinical data from CART-treated patients with cancer. This QSP model is a valuable tool for deepening our understanding of how the mechanism of action connects to the clinical outcomes and, therefore, may serve as an important model-based platform to guide the development and personalized dosing of the CART therapy.
嵌合抗原受体 T 细胞(CART)疗法是一种新的有前途的癌症疗法。然而,在接受 CART 治疗的患者中,由于细胞因子释放综合征(CRS)而出现严重毒性,突显了这种新疗法的潜在危险。疾病负担和 CART 剂量是与 CRS 相关的潜在因素,但这些因素与 CRS 严重程度之间的详细关系在很大程度上尚不清楚。在这项研究中,定量系统药理学(QSP)方法用于量化人类受试者中 CART 剂量、疾病负担和促炎细胞因子之间的复杂关系,并深入了解 CART 治疗开发过程中临床毒性/疗效的决定因素。CART 的扩增和 B 细胞的消除与疾病负担比给予的 CART 剂量更密切相关。据我们所知,这是第一个可以描述癌症患者接受 CART 治疗的观察性临床数据的 QSP 模型。该 QSP 模型是深入了解作用机制如何与临床结果相关联的有价值的工具,因此,它可以作为一个重要的基于模型的平台,指导 CART 治疗的开发和个性化给药。