Clinical progress in the development of CAR T cells to treat malignant glioma.

IF 3.2 2区 医学 Q2 CLINICAL NEUROLOGY
Journal of Neuro-Oncology Pub Date : 2025-02-01 Epub Date: 2024-12-18 DOI:10.1007/s11060-024-04909-7
Eric P Grewal, Brian V Nahed, Bob S Carter, Elizabeth R Gerstner, William T Curry, Marcela V Maus, Bryan D Choi
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引用次数: 0

Abstract

Context: Chimeric antigen receptor (CAR) T cell therapy is an exciting modality of immunotherapy that has revolutionized the treatment of hematologic malignancies. However, translating this success to malignant gliomas such as glioblastoma (GBM) and diffuse midline glioma (DMG) remains a formidable challenge due to multiple biologic, anatomic, and immunologic factors. Despite these hurdles, a number of clinical trials deployed over the last decade have increased optimism for the potential of CAR T cell therapy in glioma treatment.

Evidence synthesis: We highlight historical and ongoing clinical trials of CAR T cell therapy in glioma, with a focus on key tumor-associated antigens such as IL-13Rα2, HER2, EGFR, EGFRvIII, EphA2, GD2, and B7-H3. Early studies established proof-of-concept for antigen-specific CAR T cell targeting, yet immune evasion mechanisms such as antigen downregulation and limited CAR T cell persistence remain significant obstacles. Recent approaches, including multiantigen targeting, alternative cell sources, and innovations in delivery routes offer promising strategies to overcome these challenges.

Conclusions: The rapid evolution of investigational CAR T cell therapies portends great potential for the future of glioma treatment. Future studies will need to refine antigen targeting strategies, optimize CAR T cell persistence, and integrate combinatorial approaches to fully harness the therapeutic potential of this modality and improve the therapeutic window against brain tumors.

CAR - T细胞治疗恶性胶质瘤的临床进展。
背景:嵌合抗原受体(CAR) T细胞治疗是一种令人兴奋的免疫治疗方式,已经彻底改变了血液恶性肿瘤的治疗。然而,由于多种生物学、解剖学和免疫因素,将这种成功转化为恶性胶质瘤,如胶质母细胞瘤(GBM)和弥漫性中线胶质瘤(DMG)仍然是一个艰巨的挑战。尽管存在这些障碍,但在过去十年中开展的一些临床试验增加了对CAR - T细胞疗法在胶质瘤治疗中的潜力的乐观情绪。证据合成:我们重点介绍了CAR - T细胞治疗胶质瘤的历史和正在进行的临床试验,重点是关键的肿瘤相关抗原,如IL-13Rα2、HER2、EGFR、EGFRvIII、EphA2、GD2和B7-H3。早期的研究建立了抗原特异性CAR - T细胞靶向的概念验证,然而免疫逃避机制,如抗原下调和有限的CAR - T细胞持久性仍然是重大障碍。最近的方法,包括多抗原靶向、替代细胞来源和递送途径的创新,为克服这些挑战提供了有希望的策略。结论:研究性CAR - T细胞疗法的快速发展预示着未来胶质瘤治疗的巨大潜力。未来的研究将需要完善抗原靶向策略,优化CAR - T细胞的持久性,并整合组合方法,以充分利用这种模式的治疗潜力,提高治疗脑肿瘤的窗口期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Neuro-Oncology
Journal of Neuro-Oncology 医学-临床神经学
CiteScore
6.60
自引率
7.70%
发文量
277
审稿时长
3.3 months
期刊介绍: The Journal of Neuro-Oncology is a multi-disciplinary journal encompassing basic, applied, and clinical investigations in all research areas as they relate to cancer and the central nervous system. It provides a single forum for communication among neurologists, neurosurgeons, radiotherapists, medical oncologists, neuropathologists, neurodiagnosticians, and laboratory-based oncologists conducting relevant research. The Journal of Neuro-Oncology does not seek to isolate the field, but rather to focus the efforts of many disciplines in one publication through a format which pulls together these diverse interests. More than any other field of oncology, cancer of the central nervous system requires multi-disciplinary approaches. To alleviate having to scan dozens of journals of cell biology, pathology, laboratory and clinical endeavours, JNO is a periodical in which current, high-quality, relevant research in all aspects of neuro-oncology may be found.
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