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人源化 CD19 CAR-T 细胞用于鼠源 CD19 CAR-T 治疗后复发或失败的复发/难治性 B-ALL 患者

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.

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Humanized CD19 CAR-T cells in relapsed/refractory B-ALL patients who relapsed after or failed murine CD19 CAR-T therapy.

PubMed 2022/04/12(内容时间) BMC Cancer Q2 · IF 4.1(JCR 2025)

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研究概要

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。

研究思路结论见上方概要

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。

展开英文摘要原文

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.

论文信息

作者
An L、Lin Y、Deng B、Yin Z、Zhao D、Ling Z、Wu T、Zhao Y
第一作者单位
Department of Hematology, Beijing Boren Hospital, No.6 South Zhengwangfen, Fengtai District, Beijing, 100070, China.China
通讯作者单位
Department of Hematology, Beijing Boren Hospital, No.6 South Zhengwangfen, Fengtai District, Beijing, 100070, China. liusy@borenhospital.com.China
期刊
BMC cancer2022 Apr 12
原文标识
PubMed 35410148 · DOI 10.1186/s12885-022-09489-1