Yuraszeck T, Kasichayanula S, Benjamin J E
Clinical Pharmacology, Modeling, and Simulation, Amgen Inc., Thousand Oaks, California, USA.
Global Development, Oncology, Amgen Inc., Thousand Oaks, California, USA.
Clin Pharmacol Ther. 2017 May;101(5):634-645. doi: 10.1002/cpt.651.
Bispecific T-cell Engagers (BiTE®) antibody constructs enable a polyclonal T-cell response to cell-surface tumor-associated antigens, bypassing the narrow specificities of T-cell receptors and the need for antigen presentation through the major histocompatibility complex pathways. Blinatumomab, a CD19xCD3 BiTE® antibody construct, received accelerated approval for the treatment of relapsed/refractory Philadelphia chromosome negative acute lymphoblastic leukemia. Herein we review the pharmacology, safety, and efficacy observed in studies of blinatumomab and other BiTE® antibody constructs. Quantitative systems pharmacology is envisioned as a means to optimize dosing decisions for trials in which BiTE® antibody constructs are administered as monotherapy or in combination with other immunotherapies.
双特异性T细胞衔接器(BiTE®)抗体构建体能够引发针对细胞表面肿瘤相关抗原的多克隆T细胞反应,绕过T细胞受体的狭窄特异性以及通过主要组织相容性复合体途径进行抗原呈递的需求。blinatumomab是一种CD19xCD3 BiTE®抗体构建体,已获得加速批准用于治疗复发/难治性费城染色体阴性急性淋巴细胞白血病。在此,我们回顾了blinatumomab和其他BiTE®抗体构建体研究中观察到的药理学、安全性和疗效。定量系统药理学被设想为一种优化给药决策的方法,用于BiTE®抗体构建体作为单一疗法或与其他免疫疗法联合给药的试验。