Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States.
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States; Department of Medicine, University of Washington, Seattle, United States.
Curr Res Transl Med. 2018 May;66(2):50-52. doi: 10.1016/j.retram.2018.03.003. Epub 2018 Apr 3.
T-cells engineered to express CD19-specific chimeric antigen receptors (CD19 CAR-T cells) can achieve high response rates in patients with refractory/relapsed (R/R) CD19+ hematologic malignancies. Nonetheless, the efficacy of CD19-specific CAR-T cell therapy can be offset by significant toxicities, such as cytokine release syndrome (CRS) and neurotoxicity. In this report of our presentation at the 2018 Second French International Symposium on CAR-T cells (CAR-T day), we describe the clinical presentations of CRS and neurotoxicity in a cohort of 133 adults treated with CD19 CAR-T cells at the Fred Hutchinson Cancer Research Center, and provide insights into the mechanisms contributing to these toxicities.
经基因工程改造表达 CD19 特异性嵌合抗原受体(CD19 CAR-T 细胞)的 T 细胞可使难治/复发(R/R)CD19+血液系统恶性肿瘤患者获得高缓解率。然而,CD19 特异性 CAR-T 细胞治疗的疗效可能会因细胞因子释放综合征(CRS)和神经毒性等显著毒性而受到影响。在我们于 2018 年第二届法国国际 CAR-T 细胞研讨会上的演讲报告中,我们描述了在 Fred Hutchinson 癌症研究中心接受 CD19 CAR-T 细胞治疗的 133 例成人患者的 CRS 和神经毒性的临床表现,并深入探讨了导致这些毒性的机制。