人源 CART22.19 治疗难治性儿童 B-ALL:指定患者队列的启示
Human CART22.19 therapy in refractory pediatric B-ALL: insights from a named-patient cohort.
CART22.19 疗法在高危儿科人群中显示出良好的安全性特征和有前景的临床活性,其双靶向设计使 CD19 阴性白血病获得疾病控制。
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Human CART22.19 therapy in refractory pediatric B-ALL: insights from a named-patient cohort.
CART22.19 疗法在高危儿科人群中显示出良好的安全性特征和有前景的临床活性,其双靶向设计使 CD19 阴性白血病获得疾病控制。
A phase 1 clinical trial of NKTR-255 with CD19-22 CAR T-cell therapy for refractory B-cell acute lymphoblastic leukemia.
我们观察到良好的疗效,9例患者中有8例(89%)达到可测量残留病灶阴性缓解。
Bispecific CAR-T cells targeting CD19/20 in patients with relapsed or refractory B cell non-Hodgkin lymphoma: a phase I/II trial.
非霍奇金淋巴瘤(NHL)是血液系统常见的恶性肿瘤,传统治疗对复发/难治性NHL(R/R NHL)患者疗效有限,尤其是弥漫大B细胞淋巴瘤(DLBCL)患者。
CD19/CD22 targeting with cotransduced CAR T cells to prevent antigen-negative relapse after CAR T-cell therapy for B-cell ALL.
这些数据提示,通过共转导实现双靶向可能预防 CAR-T 细胞治疗后的抗原阴性复发。
Correction: CD19/CD22 bispecific CAR-T cells for MRD-positive adult B cell acute lymphoblastic leukemia: a phase I clinical study.
CD19/CD22 bispecific CAR-T cells for MRD-positive adult B cell acute lymphoblastic leukemia: a phase I clinical study.
Dual targeting of CD19 and CD22 against B-ALL using a novel high-sensitivity aCD22 CAR.
识别 CD19 的 CAR T 细胞可有效治疗复发/难治性 B-ALL 和 DLBCL。
CD34+CD19-CD22+ B-cell progenitors may underlie phenotypic escape in patients treated with CD19-directed therapies.
我们的数据表明,白血病前期的 CD34+CD19-CD22+ 祖细胞是 CD19 靶向免疫治疗后表型逃逸的基础,并支持正在进行的旨在将 CD19/CD22 双靶向作为减少 CD19- 复发策略的临床研究。
CAR T cells with dual targeting of CD19 and CD22 in pediatric and young adult patients with relapsed or refractory B cell acute lymphoblastic leukemia
我们开展了一项针对复发或难治性B-ALL儿童及年轻成人患者(n = 15)的1期试验,以测试AUTO3——表达抗CD19和抗CD22 CAR的自体转导T细胞(AMELIA试验,EUDRA CT 2016-004680-39)。
Exploring current evidence on bispecific CAR-T cell therapy for acute leukemias: a systematic review.
双特异性CAR-T细胞疗法在管理急性白血病方面比传统CAR-T细胞更有效。未来的研究应侧重于开发多样化的靶点并推进至临床试验。
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