医学
Blinatumoab公司
淋巴细胞白血病
耐火材料(行星科学)
嵌合抗原受体
CD19
急性淋巴细胞白血病
肿瘤科
汽车T细胞治疗
细胞因子释放综合征
白血病
内科学
免疫学
免疫疗法
抗原
癌症
物理
天体生物学
作者
Yixin Zhai,Ju Hong,Jinhuan Wang,Yanan Jiang,Wenqi Wu,Yangyang Lv,Jing Guo,Linyan Tian,Huimeng Sun,Yuhang Li,Cheng Li,Hongjie Zhan,Zhigang Zhao
标识
DOI:10.1080/17474086.2023.2298732
摘要
The CAR T-cell therapy group exhibited a higher likelihood of CR rate than the blinatumomab group in every analysis regardless of adjustment subgroups. CAR T-cell therapy was associated with a significantly prolonged overall survival (OS) and relapse-free survival (RFS) compared with blinatumomab (2-year OS 55% vs 25%; 2-year RFS 40% vs 22%). CAR T-cell therapy was more effective for achieving CR and bridging to allogeneic hematopoietic stem cell transplantation (allo-SCT) than blinatumomab (2-year OS 75% vs. 57%). An emerging role for blinatumomab is as a bridging agent pre-SCT, and for patients who achieve an MRD-negative state pre-SCT, post-SCT outcomes are expected to be the same as CAR-T. For adverse effects (AEs), blinatumomab was associated with a lower rate of grade ≥3 hematological toxicity, CRS, and neurological events.
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