医学
套细胞淋巴瘤
嵌合抗原受体
细胞因子释放综合征
淋巴瘤
弥漫性大B细胞淋巴瘤
癌症研究
CD19
T细胞
耐火材料(行星科学)
肿瘤科
内科学
抗原
免疫学
免疫系统
物理
天体生物学
作者
Patrick M. Reagan,Jonathan W. Friedberg
出处
期刊:Future Oncology
[Future Medicine]
日期:2021-01-15
卷期号:17 (11): 1269-1283
被引量:20
标识
DOI:10.2217/fon-2020-0291
摘要
Axicabtagene ciloleucel and brexucabtagene autoleucel are anti-CD19 T-cell therapies that utilize the same second-generation chimeric antigen receptor with a CD28 costimulatory subunit. They have demonstrated high rates of response in high-risk patients with relapsed and refractory B-cell malignancies in multicenter clinical trials, including diffuse large B-cell and mantle cell lymphomas. The high clinical activity has led to the US FDA approval of axicabtagene ciloleucel for diffuse large B-cell lymphoma, and brexucabtagene autoleucel for mantle cell lymphoma. While they are highly effective, they have significant toxicities, including cytokine release syndrome and neurologic toxicities, which can be severe and require specialized management. This review will discuss the development, efficacy and safety of axicabtagene ciloleucel and brexucabtagene autoleucel in B-cell lymphomas.
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