Blinatumoab公司
医学
免疫疗法
肿瘤科
淋巴瘤
细胞因子释放综合征
滤泡性淋巴瘤
内科学
耐火材料(行星科学)
临床试验
嵌合抗原受体
免疫学
重症监护医学
白血病
淋巴细胞白血病
癌症
生物
天体生物学
作者
Rakesh Awasthi,Harald J. Maier,Jie Zhang,Stephen Lim
标识
DOI:10.1080/21645515.2023.2210046
摘要
The emergence of cell and gene therapies has dramatically changed the treatment paradigm in oncology and other therapeutic areas. Kymriah® (tisagenlecleucel), a CD19-directed genetically modified autologous T-cell immunotherapy, is currently approved in major markets for the treatment of relapsed/refractory (r/r) pediatric and young adult acute lymphoblastic leukemia, r/r diffuse large B-cell lymphoma, and r/r follicular lymphoma. This article presents a high-level overview of the clinical development journey of tisagenlecleucel, including its efficacy outcomes and safety considerations.
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