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学术性即时抗 CD19CAR-T 细胞产品 varnimcabtagene autoleucel(ARI-0001 细胞)在治疗复发/难治性 B 细胞非霍奇金淋巴瘤中显示出疗效和安全性

英文原题:The academic point-of-care anti-CD19 chimeric antigen receptor T-cell product varnimcabtagene autoleucel (ARI-0001 cells) shows efficacy and safety in the treatment of relapsed/refractory B-cell non-Hodgkin lymphoma.

查看英文原题

The academic point-of-care anti-CD19 chimeric antigen receptor T-cell product varnimcabtagene autoleucel (ARI-0001 cells) shows efficacy and safety in the treatment of relapsed/refractory B-cell non-Hodgkin lymphoma.

PubMed 2023/10/31(内容时间) Br J Haematol Q2 · IF 3.6(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

Varnimcabtagene autoleucel(var-cel)是一种学术性抗CD19嵌合抗原受体(CAR)产品,用于在CAR-T19-BE-01试验中治疗非霍奇金淋巴瘤(NHL)。在此,我们报告接受var-cel治疗的NHL患者的更新结局。将B细胞恢复情况与急性淋巴细胞白血病(ALL)患者进行比较。共45例NHL患者接受治疗。细胞因子释放综合征(任何级别)发生于84%的患者(4%为≥3级),神经毒性发生于7%(2%为≥3级)。第+100天的客观缓解率为73%,3年缓解持续率为56%。3年无进展生存率和总生存率分别为40%和52%。高乳酸脱氢酶是唯一对无进展生存率有影响的协变量。与ALL相比,NHL患者3年B细胞恢复发生率较低(25% vs. 60%)。总之,在NHL患者中,var-cel的毒性可控,而B细胞恢复较ALL显著延长。该试验注册号为NCT03144583。

展开英文摘要原文

Varnimcabtagene autoleucel (var-cel) is an academic anti-CD19 chimeric antigen receptor (CAR) product used for the treatment of non-Hodgkin lymphoma (NHL) in the CART19-BE-01 trial.

Here we report updated outcomes of patients with NHL treated with var-cel. B-cell recovery was compared with patients with acute lymphoblastic leukaemia (ALL). Forty-five patients with NHL were treated. Cytokine release syndrome (any grade) occurred in 84% of patients (4% grade ≥3) and neurotoxicity in 7% (2% grade ≥3).

The objective response rate was 73% at Day +100, and the 3-year duration of response was 56%. The 3-year progression-free and overall survival were 40% and 52% respectively. High lactate dehydrogenase was the only covariate with an impact on progression-free survival. The 3-year incidence of B-cell recovery was lower in patients with NHL compared to ALL (25% vs. 60%).

In conclusion, in patients with NHL, the toxicity of var-cel was manageable, while B-cell recovery was significantly prolonged compared to ALL. This trial was registered as NCT03144583.

论文信息

作者
Martínez-Cibrián N、Ortiz-Maldonado V、Español-Rego M、Blázquez A、Cid J、Lozano M、Magnano L、Giné E
单位
Department of Hematology, Hospital Clínic, Barcelona, Spain.Spain
文献类型
非美国政府资助研究
期刊
British journal of haematology2024 Feb
原文标识
PubMed 37905734 · DOI 10.1111/bjh.19170