The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer Discov. 2023 Sep 6;13(9):1961-1963. doi: 10.1158/2159-8290.CD-23-0735.
In this issue of Cancer Discovery, Dickinson and colleagues present clinical data from a first-in-human study of YTB323, a novel autologous CD19-directed chimeric antigen receptor T-cell therapy generated on the T-Charge platform with preserved naive state and stemness phenotypes. Treatment with YTB323 achieved high overall response rates, durable complete remissions, and good overall safety. Their cell doses are up to 25-fold lower than with tisagenlecleucel. See related article by Dickinson et al., p. 1982 (10).
在本期《癌症发现》中,Dickinson 及其同事报告了 YTB323 的首次人体研究的临床数据,YTB323 是一种新型的自体 CD19 导向嵌合抗原受体 T 细胞疗法,在 T-Charge 平台上生成,保留了幼稚状态和干性表型。YTB323 的治疗实现了高总缓解率、持久的完全缓解和良好的总体安全性。他们的细胞剂量比 tisagenlecleucel 低 25 倍。参见 Dickinson 等人的相关文章,第 1982 页(10)。