胶质母细胞瘤(GBM)有效治疗的组合方法:现状和未来。

IF 4.3 4区 医学 Q2 IMMUNOLOGY
International Reviews of Immunology Pub Date : 2022-01-01 Epub Date: 2022-08-08 DOI:10.1080/08830185.2022.2101647
Sweety Asija, Abhishek Chatterjee, Sandhya Yadav, Godhanjali Chekuri, Atharva Karulkar, Ankesh Kumar Jaiswal, Jayant S Goda, Rahul Purwar
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引用次数: 11

摘要

胶质母细胞瘤的侵袭性和复发性是多因素的,归因于其生物学异质性、代谢信号通路功能失调、刚性血脑屏障、胶质瘤细胞的干性对标准治疗的固有抵抗、免疫抑制的肿瘤微环境、缺氧和新生血管生成,这些都是精心策划的,并创造了肿瘤自身高度促肿瘤发生的环境。一旦事件在这些组成部分之间开始传递,最终仅使用平衡的当代治疗护理(包括最大切除,替莫唑胺放疗和化疗)来控制级联变得困难。在过去的几十年里,现代治疗方式的实施在一定程度上显示出了益处,但没有取得显著的总体生存益处。因此,对先进的多面组合策略的需求尚未得到满足。近年来,分子生物学的最新进展、创新疗法的发展和新的给药平台导致了胶质瘤治疗的范式转变。几十年的研究已经导致了几种治疗分子的出现,包括免疫疗法,如免疫检查点阻断,溶瘤病毒疗法,过继细胞疗法,纳米颗粒,CED和BNCT,每一个都有独特的能力来克服上述挑战,目前的研究。近年来,为了克服GBM细胞及其TME提出的多因子耐药,出现了创新的组合策略。这篇综述讨论了当代和研究性治疗GBM的组合策略,并总结了迄今为止积累的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combinatorial approaches to effective therapy in glioblastoma (GBM): Current status and what the future holds.

The aggressive and recurrent nature of glioblastoma is multifactorial and has been attributed to its biological heterogeneity, dysfunctional metabolic signaling pathways, rigid blood-brain barrier, inherent resistance to standard therapy due to the stemness property of the gliomas cells, immunosuppressive tumor microenvironment, hypoxia and neoangiogenesis which are very well orchestrated and create the tumor's own highly pro-tumorigenic milieu. Once the relay of events starts amongst these components, eventually it becomes difficult to control the cascade using only the balanced contemporary care of treatment consisting of maximal resection, radiotherapy and chemotherapy with temozolamide. Over the past few decades, implementation of contemporary treatment modalities has shown benefit to some extent, but no significant overall survival benefit is achieved. Therefore, there is an unmet need for advanced multifaceted combinatorial strategies. Recent advances in molecular biology, development of innovative therapeutics and novel delivery platforms over the years has resulted in a paradigm shift in gliomas therapeutics. Decades of research has led to emergence of several treatment molecules, including immunotherapies such as immune checkpoint blockade, oncolytic virotherapy, adoptive cell therapy, nanoparticles, CED and BNCT, each with the unique proficiency to overcome the mentioned challenges, present research. Recent years are seeing innovative combinatorial strategies to overcome the multifactorial resistance put forth by the GBM cell and its TME. This review discusses the contemporary and the investigational combinatorial strategies being employed to treat GBM and summarizes the evidence accumulated till date.

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来源期刊
CiteScore
11.00
自引率
4.00%
发文量
24
期刊介绍: This review journal provides the most current information on basic and translational research in immunology and related fields. In addition to invited reviews, the journal accepts for publication articles and editorials on relevant topics proposed by contributors. Each issue of International Reviews of Immunology contains both solicited and unsolicited review articles, editorials, and ''In-this-Issue'' highlights. The journal also hosts reviews that position the authors'' original work relative to advances in a given field, bridging the gap between annual reviews and the original research articles. This review series is relevant to all immunologists, molecular biologists, microbiologists, translational scientists, industry researchers, and physicians who work in basic and clinical immunology, inflammatory and allergic diseases, vaccines, and additional topics relevant to medical research and drug development that connect immunology to disciplines such as oncology, cardiovascular disease, and metabolic disorders. Covered in International Reviews of Immunology: Basic and developmental immunology (innate and adaptive immunity; inflammation; and tumor and microbial immunology); Clinical research (mechanisms of disease in man pertaining to infectious diseases, autoimmunity, allergy, oncology / immunology); and Translational research (relevant to biomarkers, diagnostics, vaccines, and drug development).
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