医学
造血干细胞移植
化疗
Blinatumoab公司
微小残留病
挽救疗法
肝静脉闭塞性疾病
肿瘤科
耐火材料(行星科学)
嵌合抗原受体
奥佐美星
内科学
疾病
干细胞
淋巴细胞白血病
白血病
重症监护医学
癌症
免疫疗法
川地34
CD33
遗传学
物理
天体生物学
生物
作者
Hagop M. Kantarjian,Nicolas Boissel,Cristina Papayannidis,Marlise R. Luskin,Matthias Stelljes,Anjali S. Advani,Elias Jabbour,Josep‐María Ribera,David I. Marks
出处
期刊:Cancer
[Wiley]
日期:2024-08-02
被引量:2
摘要
Abstract Inotuzumab ozogamicin (InO) is an antibody‐drug conjugate approved for the treatment of relapsed/refractory B‐cell acute lymphoblastic leukemia (ALL). Several clinical trials are investigating InO in combination with low‐intensity chemotherapy or other anti‐ALL–targeted therapies in the salvage and frontline settings, notably in older adults who often cannot tolerate intensive chemotherapy and tend to have higher‐risk disease. InO is also increasingly used to bridge patients to hematopoietic stem cell transplantation (HSCT), in sequence with chimeric antigen receptor T‐cell therapy, to eliminate measurable residual disease and to prevent post‐HSCT relapse. Veno‐occlusive disease/sinusoidal obstruction syndrome is a potential complication of InO treatment, particularly when followed by HSCT. Herein, the authors review the historical development and current status of InO, strategies for mitigating the risk of InO‐related veno‐occlusive disease/sinusoidal obstruction syndrome, and future directions for InO research and clinical use.
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