肿瘤细胞治疗研究
英文原题:Humanized CD19 CAR-T cells in relapsed/refractory B-ALL patients who relapsed after or failed murine CD19 CAR-T therapy.
Humanized CD19 CAR-T cells in relapsed/refractory B-ALL patients who relapsed after or failed murine CD19 CAR-T therapy.
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人源化 CD19 CAR-T 细胞疗法可能是对既往鼠源 CD19 CAR-T 治疗后复发或耐药的 CD19 阳性 B-ALL 患者的一种治疗选择,hCD19 CAR-T 后桥接 allo-HCT 使 CR 患者获得了更长的缓解期。然而,对 hCD19 CAR-T 无应答者的预后仍然很差。
对于鼠源 CD19 (mCD19) CAR-T 治疗后的 CD19 阳性复发/难治性 B 细胞急性淋巴细胞白血病 (r/r B-ALL),由于 mCD19 CAR 引起的抗鼠单链可变区片段 (scFv) 抗体,再次输注 mCD19 CAR-T 细胞可能无效。为克服这种免疫原性,我们应用人源化 CD19 (hCD19) CAR-T 细胞治疗既往接受过 mCD19 CAR-T 治疗的 r/r B-ALL 患者。
纳入19例儿童和成人患者,其中16例在mCD19 CAR-T 后复发,3例原发耐药。所有患者骨髓和/或髓外病变中原始细胞均超过5%,且仍显示CD19抗原表达。人源化CD19-CAR为慢病毒载体,携带含4-1-BB共刺激域和CD3信号域的第二代CAR。采集患者来源细胞用于制备CAR-T 细胞,输注的hCD19 CAR-T 细胞中位剂量为2.4 10 5 /kg(范围,1.0-18.0 10 5 /kg)。
hCD19 CAR-T 的完全缓解(CR)率为 68%(13/19)。在 13 例缓解患者中,11 例接受了异基因造血细胞移植(allo-HCT)(3 例为第二次 HCT),10 例维持 CR;接受 allo-HCT 后随访的 11 例患者 12-18 个月无事件生存率为 91%,所有 CR 患者为 69%。6 例对 hCD19 CAR-T 无反应,3 例死于疾病进展;另有 3 例接受了挽救性第二次移植,其中 2 例再次复发(1 例死亡)。细胞因子释放综合征(CRS)发生于 95%(18/19)的患者,大多数 CRS 事件为 1 级和 2 级(n = 17),仅有 1 例 4 级 CRS。2 例出现 1 级神经毒性。
For CD19-positive relapsed/refractory B-cell acute lymphoblastic leukemia (r/r B-ALL) after treatment with murine CD19 (mCD19) CAR-T, the reinfusion of mCD19 CAR-T cells may be ineffective due to anti-mouse single-chain variable fragment (scFv) antibody caused by mCD19 CAR. To overcome this immunogenicity, we applied humanized CD19 (hCD19) CAR-T cells to treat r/r B-ALL patients with prior mCD19 CAR-T therapy.
Nineteen pediatric and adult patients were included, 16 relapsed after and 3 were primarily resistant to mCD19 CAR-T. All patients presented with more than 5% blasts in bone marrow and/or extramedullary disease, and still showed CD19 antigen expression. Humanized CD19-CARs were lentiviral vectors carrying a second generation CAR with 4-1-BB co-stimulatory and CD3 signaling domains. Patient-derived cells were collected for producing CAR-T cells, the median dose of infused hCD19 CAR-T cells was 2.4 10 5 /kg (range, 1.0-18.0 10 5 /kg).
hCD19 CAR-T resulted in a complete remission (CR) rate of 68% (13/19). Among 13 remission patients, 11 underwent allogeneic hematopoietic cell transplantation (allo-HCT) (3 were second HCT) and 10 remained in CR; the event-free survival rates at 12-18 months were 91% in 11 patients received following allo-HCT and 69% in all CR patients. Six cases had no response to hCD19 CAR-T, 3 died of disease progression; another 3 received salvage second transplantation, of them, 2 relapsed again (one died). Cytokine release syndrome (CRS) occurred in 95% (18/19) of patients, most CRS events were grade 1 and grade 2 (n = 17), there was only one grade 4 CRS. Two cases experienced grade 1 neurotoxicity.
Humanized CD19 CAR-T cell therapy could be a treatment option for CD19-positive B-ALL patients who relapsed after or resisted prior murine CD19 CAR-T, hCD19 CAR-T followed by allo-HCT provided a longer remission in CR patients. Nevertheless, the prognosis of non-responders to hCD19 CAR-T remained dismal. TRIAL REGISTRATION: Chinese Clinical Trial Registry/WHO International Clinical Trial Registry ( ChiCTR1900024456 , URL: www.chictr.org.cn ); registered on July 12, 2019.
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