Frey Noelle
Hospital of the University of Pennsylvania Philadelphia, PA, United States.
Best Pract Res Clin Haematol. 2017 Sep;30(3):275-281. doi: 10.1016/j.beha.2017.07.009. Epub 2017 Aug 3.
Chimeric Antigen Receptor (CAR) T cells that have been engineered to target CD19 have shown great promise in patients with relapsed and refractory B cell acute lymphocytic leukemia with remission rates of 70-90%. Some remissions have successfully bridged patients to a curable allogeneic stem cell transplant, some responses have been durable without further treatment, and some patients have achieved durable remissions for relapsed ALL after allogeneic stem cell transplant. Cytokine release syndrome, correlating with the in vivo activation and expansion of T cells, and neurologic toxicity are the most significant side effects and approaches to better understand and manage these events are the subject of ongoing clinical trials. The decision to intervene with CARTs requires an individualized approach taking into consideration patient, disease and therapy related factors.
经过基因工程改造以靶向CD19的嵌合抗原受体(CAR)T细胞,在复发难治性B细胞急性淋巴细胞白血病患者中显示出巨大潜力,缓解率达70%-90%。一些缓解成功地使患者过渡到可治愈的异基因干细胞移植,一些反应在无需进一步治疗的情况下持久存在,还有一些患者在异基因干细胞移植后复发的急性淋巴细胞白血病中实现了持久缓解。与T细胞在体内的激活和扩增相关的细胞因子释放综合征和神经毒性是最显著的副作用,更好地理解和管理这些事件的方法是正在进行的临床试验的主题。决定是否使用CAR T细胞进行干预需要采取个体化方法,同时考虑患者、疾病和治疗相关因素。