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A novel dominant-negative PD-1 armored anti-CD19 CAR T cell is safe and effective against refractory/relapsed B cell lymphoma

机译:一种新的主​​导阴性PD-1装甲抗CD19 Car T细胞对于难治性/复发的B细胞淋巴瘤是安全可有效的

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Refractory/relapsed B cell lymphoma patients who received the available anti-CD19 chimeric antigen receptor (CAR) T cells may still experience a short duration of remission. Here in this study, we evaluated the safety and efficacy of a novel dominant-negative programmed cell death-1 (PD-1) armored anti-CD19 CAR T cells. A total of 9 patients (including 4 diffuse large B cell lymphomas, DLBCL, 2 transformed follicular lymphomas, TFL, and 3 follicular lymphomas, FL) received the novel CAR T cells infusion at a dose of more than 1?×?106/kg. Grade ≥ 3 cytokine release syndrome (CRS) and neurotoxicity were observed in 11.1% (n?=?1/9) and 11.1% (n?=?1/9) of patients, respectively. The overall response rate (ORR) was 77.8% (n?=?7/9) and complete response (CR) rate was 55.6% (n?=?5/9). Two patients have ongoing CR (all at 20+ months). CAR T cells expanded after infusion and continued to be detectable at 12+ months in patients with ongoing CR. This novel CD19-CAR T cell was safe and effective with durable remissions in patients with refractory/relapsed B cell lymphoma.
机译:接受可用的抗CD19嵌合抗原受体(汽车)T细胞的难治性/复发的B细胞淋巴瘤患者可能仍然经历缓解持续时间。在本研究中,我们评估了一种新型优势阴性程序细胞死亡-1(PD-1)铠装抗CD19 Car T细胞的安全性和功效。共有9名患者(包括4个弥漫性大B细胞淋巴瘤,DLBCL,2种转化的滤泡淋巴瘤,TFL和3个滤泡淋巴瘤,FL)在超过1的剂量下输注新的汽车T细胞输注?×106 / kg 。 ≥3分细胞因子释放综合征(CRS)和神经毒性分别观察到患者的11.1%(n?= 1/9)和11.1%(n?= 1/9)。整体反应率(ORR)为77.8%(n?= 7/9),完全反应(Cr)率为55.6%(n?= 5/9)。两名患者持续了CR(均在20多个月内)。在进行CR患者的患者中,CAR T细胞扩增并继续在12个月内持续可检测。这种新型CD19-CAR T细胞对于耐火/复发的B细胞淋巴瘤患者的耐用剩余安全和有效。

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