Mechanisms of Therapeutic Resistance and Recent Advances in Glioblastoma Treatment

IF 3.3 4区 医学 Q3 CELL BIOLOGY
Immunology & Cell Biology Pub Date : 2026-08-04 Epub Date: 2026-07-03 DOI:10.1111/imcb.70144
Emerson Achari, Farah Ahmady-Nield, Amit Sharma, Ingo G. H. Schmidt-Wolf, Jarek Maciaczyk, Rodney B. Luwor, Adrian A. Achuthan
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引用次数: 0

Abstract

High-grade central nervous system cancers incur a significant burden of care on society. The combination of therapeutic resistance and high mortality makes it both a challenging target and a devastating diagnosis. Of these, one in two is characterized as glioblastoma (GBM) with a median survival rate of only 13.5 months with the current standard of therapy. Modern interventions, such as PD-1 and CTLA-4 checkpoint inhibition and autologous CAR T cell delivery, remain stymied by both the difficult nature of drug delivery to the brain and the inherent immunosuppressive tumor microenvironment. However, recent advances in the characterization of GBM have unveiled promising new therapeutic avenues aiming to target and eliminate the tumor. In this review, we summarize the mechanisms through which GBM is initiated, localized, and eludes therapy responses and provide an update on recent advances made within this therapeutic space to overcome GBM-mediated immunosuppression. We also discuss the challenges with current and next generational treatment strategies before finally exploring the landscape of potential future therapeutic targets.

胶质母细胞瘤的耐药机制及治疗进展。
高级别中枢神经系统癌症给社会带来了沉重的医疗负担。治疗耐药性和高死亡率的结合使得它既是一个具有挑战性的目标,也是一个毁灭性的诊断。其中,二分之一的患者表现为胶质母细胞瘤(GBM),按照目前的治疗标准,患者的中位生存期仅为13.5个月。现代干预措施,如PD-1和CTLA-4检查点抑制和自体CAR - T细胞递送,仍然受到药物递送到大脑的困难性质和固有的免疫抑制肿瘤微环境的阻碍。然而,最近在GBM表征方面的进展揭示了旨在靶向和消除肿瘤的有希望的新治疗途径。在这篇综述中,我们总结了GBM的启动、局部化和逃避治疗反应的机制,并提供了在治疗领域克服GBM介导的免疫抑制的最新进展。在最终探索潜在的未来治疗靶点之前,我们还讨论了当前和下一代治疗策略的挑战。
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
Immunology & Cell Biology
Immunology & Cell Biology 医学-免疫学
CiteScore
7.50
自引率
2.50%
发文量
98
审稿时长
4-8 weeks
期刊介绍: The Australasian Society for Immunology Incorporated (ASI) was created by the amalgamation in 1991 of the Australian Society for Immunology, formed in 1970, and the New Zealand Society for Immunology, formed in 1975. The aim of the Society is to encourage and support the discipline of immunology in the Australasian region. It is a broadly based Society, embracing clinical and experimental, cellular and molecular immunology in humans and animals. The Society provides a network for the exchange of information and for collaboration within Australia, New Zealand and overseas. ASI members have been prominent in advancing biological and medical research worldwide. We seek to encourage the study of immunology in Australia and New Zealand and are active in introducing young scientists to the discipline.
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