Blinatumoab公司
嵌合抗原受体
医学
淋巴细胞白血病
靶向治疗
CD19
免疫学
肿瘤科
免疫疗法
移植
挽救疗法
白血病
内科学
抗原
化疗
癌症
免疫系统
作者
Sajad Khazal,Partow Kebriaei
标识
DOI:10.1016/j.clml.2020.06.011
摘要
Despite high complete remission (CR) rates, relapse remains a significant problem among subsets of patients with B acute lymphoblastic leukemia (ALL), and is associated with poor prognosis. The recent Food and Drug Administration approval of highly effective immunotherapies for B-lineage ALL (B-ALL), blinatumomab, inotuzumab ozogamicin, and tisagenlecleucel, a chimeric antigen receptor (CAR) modified T-cell therapy, targeting CD19, or CD22, have dramatically changed the therapeutic landscape for the treatment of B-ALL, resulting in high rates of deep and durable remissions. Therefore, there is now debate regarding the role of allogeneic hematopoietic cell transplantation (HCT) in this new landscape. Herein, we review these novel agents, and discuss the sequence of therapy, including allogeneic HCT in B-ALL.
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