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患者来源的胶质母细胞瘤类器官作为评估临床CAR-T细胞治疗反应的实时化身。

Patient-derived glioblastoma organoids as real-time avatars for assessing responses to clinical CAR-T cell therapy.

作者信息

Logun Meghan, Wang Xin, Sun Yusha, Bagley Stephen J, Li Nannan, Desai Arati, Zhang Daniel Y, Nasrallah MacLean P, Pai Emily Ling-Lin, Oner Bike Su, Plesa Gabriela, Siegel Donald, Binder Zev A, Ming Guo-Li, Song Hongjun, O'Rourke Donald M

机构信息

Glioblastoma Translational Center of Excellence, Abramson Cancer Center, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA; Department of Neurosurgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.

Department of Neuroscience and Mahoney Institute for Neurosciences, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.

出版信息

Cell Stem Cell. 2025 Feb 6;32(2):181-190.e4. doi: 10.1016/j.stem.2024.11.010. Epub 2024 Dec 9.

Abstract

Patient-derived tumor organoids have been leveraged for disease modeling and preclinical studies but rarely applied in real time to aid with interpretation of patient treatment responses in clinics. We recently demonstrated early efficacy signals in a first-in-human, phase 1 study of dual-targeting chimeric antigen receptor (CAR)-T cells (EGFR-IL13Rα2 CAR-T cells) in patients with recurrent glioblastoma. Here, we analyzed six sets of patient-derived glioblastoma organoids (GBOs) treated concurrently with the same autologous CAR-T cell products as patients in our phase 1 study. We found that CAR-T cell treatment led to target antigen reduction and cytolysis of tumor cells in GBOs, the degree of which correlated with CAR-T cell engraftment detected in patients' cerebrospinal fluid (CSF). Furthermore, cytokine release patterns in GBOs mirrored those in patient CSF samples over time. Our findings highlight a unique trial design and GBOs as a valuable platform for real-time assessment of CAR-T cell bioactivity and insights into immunotherapy efficacy.

摘要

患者来源的肿瘤类器官已被用于疾病建模和临床前研究,但很少实时应用于临床以辅助解读患者的治疗反应。我们最近在一项针对复发性胶质母细胞瘤患者的双靶点嵌合抗原受体(CAR)-T细胞(EGFR-IL13Rα2 CAR-T细胞)的首次人体1期研究中展示了早期疗效信号。在此,我们分析了六组患者来源的胶质母细胞瘤类器官(GBO),它们与我们1期研究中的患者同时接受相同的自体CAR-T细胞产品治疗。我们发现,CAR-T细胞治疗导致GBO中肿瘤细胞的靶抗原减少和细胞溶解,其程度与在患者脑脊液(CSF)中检测到的CAR-T细胞植入相关。此外,随着时间的推移,GBO中的细胞因子释放模式与患者CSF样本中的模式相似。我们的研究结果突出了一种独特的试验设计以及GBO作为实时评估CAR-T细胞生物活性和深入了解免疫治疗疗效的宝贵平台。

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