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基于嵌合抗原受体 T 细胞的模型的细胞动力学分析。

Tisagenlecleucel Model-Based Cellular Kinetic Analysis of Chimeric Antigen Receptor-T Cells.

机构信息

Novartis Institutes for BioMedical Research, Cambridge, Massachusetts, USA.

Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

出版信息

CPT Pharmacometrics Syst Pharmacol. 2019 May;8(5):285-295. doi: 10.1002/psp4.12388. Epub 2019 Mar 7.

Abstract

Tisagenlecleucel is a chimeric antigen receptor-T cell therapy that facilitates the killing of CD19 B cells. A model was developed for the kinetics of tisagenlecleucel and the impact of therapies for treating cytokine release syndrome (tocilizumab and corticosteroids) on expansion. Data from two phase II studies in pediatric and young adult relapsed/refractory B cell acute lymphoblastic leukemia were pooled to evaluate this model and evaluate extrinsic and intrinsic factors that may impact the extent of tisagenlecleucel expansion. The doubling time, initial decline half-life, and terminal half-life for tisagenlecleucel were 0.78, 4.3, and 220 days, respectively. No impact of tocilizumab or corticosteroids on the expansion rate was observed. This work represents the first mixed-effect model-based analysis of chimeric antigen receptor-T cell therapy and may be clinically impactful as future studies examine prophylactic interventions in patients at risk of higher grade cytokine release syndrome and the effects of these interventions on chimeric antigen receptor-T cell expansion.

摘要

tisagenlecleucel 是一种嵌合抗原受体-T 细胞疗法,可促进 CD19 B 细胞的杀伤。我们建立了一个模型来描述 tisagenlecleucel 的动力学以及治疗细胞因子释放综合征(托珠单抗和皮质类固醇)对其扩增的影响。对来自儿科和年轻成人复发/难治性 B 细胞急性淋巴细胞白血病的两项 II 期研究的数据进行了汇总,以评估该模型,并评估可能影响 tisagenlecleucel 扩增程度的外在和内在因素。tisagenlecleucel 的倍增时间、初始下降半衰期和终末半衰期分别为 0.78、4.3 和 220 天。未观察到托珠单抗或皮质类固醇对扩增率的影响。这是对嵌合抗原受体-T 细胞疗法的首次基于混合效应模型的分析,可能具有临床意义,因为未来的研究将检查有发生更高等级细胞因子释放综合征风险的患者的预防性干预措施,以及这些干预措施对嵌合抗原受体-T 细胞扩增的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a55/6539725/8f49d8c6341b/PSP4-8-285-g001.jpg

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