Autologous CD19-directed chimeric antigen receptor-T cell is an effective and safe treatment to refractory or relapsed diffuse large B-cell lymphoma

嵌合抗原受体 医学 弥漫性大B细胞淋巴瘤 癌症研究 淋巴瘤 受体 CD19 免疫学 耐火材料(行星科学) 抗原 内科学 免疫疗法 免疫系统 生物 天体生物学
作者
Fang Bao,Wei Wan,Ting He,Feifei Qi,Guanghua Liu,Kai Hu,Xin‐an Lu,Ping Yang,Fei Dong,Jing Wang,Hongmei Jing
出处
期刊:Cancer Gene Therapy [Springer Nature]
卷期号:26 (7-8): 248-255 被引量:23
标识
DOI:10.1038/s41417-018-0073-7
摘要

Patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) have a poor prognosis. Chimeric antigen receptor (CAR) modified T cells targeting CD19 hold great promise to improve the complete response rates of DLBCL patients compared with conventional therapies. Here, we conducted a clinical trial to evaluate the efficacy and safety of CAR-T cells. Five patients with relapsed or refractory DLBCL were treated with autologous T cells expressing the 19-41BBz chimeric antigen receptor (CAR) specifically targeted the CD19 antigen (IM19 CAR-T). The development of cytokine release syndrome (CRS) was observed. And the efficacy of IM19 CAR-T cell treatment was measured with positron emission tomography (PET)-computed tomography (CT). Of the four patients evaluable for response, two obtained complete responses (CRs), one obtained partial response (PR), and one had stable disease (SD). Remarkably, among the five patients, only one developed grade 2 CRS while the others only elicited grade 1 CRS. Additionally, the efficacy and safety of IM19 CAR-T cells were correlated with the peak blood level and persistence of CAR-T cells, as well as the immunophenotype of T-cell subsets. Overall, this study indicates the feasibility and effectiveness of IM19 CAR-T cells in the treatment of refractory or relapsed diffuse large B-cell lymphoma.
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