首页> 美国卫生研究院文献>Neuro-Oncology >RBTT-12. A PHASE I STUDY OF EGFRVIII-DIRECTED CAR T CELLS COMBINED WITH PD-1 INHIBITION IN PATIENTS WITH NEWLY DIAGNOSED MGMT-UNMETHYLATED GLIOBLASTOMA: TRIAL IN PROGRESS
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RBTT-12. A PHASE I STUDY OF EGFRVIII-DIRECTED CAR T CELLS COMBINED WITH PD-1 INHIBITION IN PATIENTS WITH NEWLY DIAGNOSED MGMT-UNMETHYLATED GLIOBLASTOMA: TRIAL IN PROGRESS

机译:RBTT-12。 I阶段研究EGFRVIII指导的CAR T细胞与新诊断的MGMT-未甲基化胶质母细胞瘤患者的PD-1抑制相结合:正在进行中的试验

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摘要

This study builds on the results of the University of Pennsylvania sponsored phase I study of a single peripheral infusion of chimeric antigen receptor (CAR) T cells targeting epidermal growth factor receptor variant III (EGFRvIII) in recurrent glioblastoma (GBM) ({"type":"clinical-trial","attrs":{"text":"NCT02209376","term_id":"NCT02209376"}}NCT02209376). A dose of 5x108 CART-EGFRvIII cells was safe, and the cells were able to expand in the host and reach the GBM tumor in the brain. In addition, there was no cross-reactivity of CART-EGFRvIII cells with wild-type EGFR normally expressed by human tissues. Some patients required tumor resection after CAR T cell infusion. In situ evaluation of the tumor microenvironment demonstrated increased and robust expression of inhibitory molecules, such as programmed death-ligand 1 (PD-L1), compared to pre–CART-EGFRvIII tumor specimens. Therefore, we hypothesized that using a combination of CART-EGFRvIII cells and a PD-1 inhibitor would improve the outcome of the treatment.
机译:本研究建立了宾夕法尼亚大学赞助阶段的结果,研究了嵌入表皮生长因子受体III(EGFRVIII)的嵌合抗原受体(轿厢)T细胞的单周输注在复发胶质细胞瘤(GBM)({“型” :“临床试验”,“attrs”:{“text”:“nct02209376”,“term_id”:“nct02209376”}} nct02209376)。剂量为5x108购物车 - EGFRVIII细胞是安全的,并且细胞能够在宿主中扩张并在大脑中达到GBM肿瘤。此外,没有人体组织通常表达的野生型EGFR的购物车-EGFRVIII细胞的交叉反应性。有些患者在汽车输注后需要肿瘤切除。与购物车前-EGFRVIII肿瘤标本相比,原位评估肿瘤微环境的抑制分子(例如编程死亡配体1(PD-L1)的增强和稳健的表达。因此,我们假设使用Cart-EGFRVIIII细胞和PD-1抑制剂的组合将改善治疗的结果。

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