Locoregional infusion of HER2-specific CAR T cells in children and young adults with recurrent or refractory CNS tumors: an interim analysis

耐受性 医学 嵌合抗原受体 加药 中期分析 免疫系统 毒性 髓母细胞瘤 临床试验 肿瘤科 内科学 免疫疗法 不利影响 免疫学 病理
作者
Nicholas A. Vitanza,Adam Johnson,Ashley Wilson,Christopher Brown,Jason K. Yokoyama,Annette Künkele,Cindy A. Chang,Stephanie D. Rawlings‐Rhea,Wenjun Huang,Kristy Seidel,Catherine M. Albert,Navin Pinto,Juliane Gust,Laura S. Finn,Jeffrey G. Ojemann,Jason N. Wright,Rimas J. Orentas,Michael Baldwin,Rebecca Gardner,Michael C. Jensen,Julie R. Park
出处
期刊:Nature Medicine [Springer Nature]
卷期号:27 (9): 1544-1552 被引量:142
标识
DOI:10.1038/s41591-021-01404-8
摘要

Locoregional delivery of chimeric antigen receptor (CAR) T cells has resulted in objective responses in adults with glioblastoma, but the feasibility and tolerability of this approach is yet to be evaluated for pediatric central nervous system (CNS) tumors. Here we show that engineering of a medium-length CAR spacer enhances the therapeutic efficacy of human erb-b2 receptor tyrosine kinase 2 (HER2)-specific CAR T cells in an orthotopic xenograft medulloblastoma model. We translated these findings into BrainChild-01 ( NCT03500991 ), an ongoing phase 1 clinical trial at Seattle Children’s evaluating repetitive locoregional dosing of these HER2-specific CAR T cells to children and young adults with recurrent/refractory CNS tumors, including diffuse midline glioma. Primary objectives are assessing feasibility, safety and tolerability; secondary objectives include assessing CAR T cell distribution and disease response. In the outpatient setting, patients receive infusions via CNS catheter into either the tumor cavity or the ventricular system. The initial three patients experienced no dose-limiting toxicity and exhibited clinical, as well as correlative laboratory, evidence of local CNS immune activation, including high concentrations of CXCL10 and CCL2 in the cerebrospinal fluid. This interim report supports the feasibility of generating HER2-specific CAR T cells for repeated dosing regimens and suggests that their repeated intra-CNS delivery might be well tolerated and activate a localized immune response in pediatric and young adult patients. In an interim analysis of a phase 1 trial, repeated intracranial infusions of HER2-specific CAR T cells were well tolerated with no observed dose-limiting toxicities in three young adult patients with CNS tumors.
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