School of Science, Shenzhen Key Laboratory of Flexible Printed Electronics Technology, Shenzhen Key Laboratory of Advanced Functional Carbon Materials Research and Comprehensive Application, Harbin Institute of Technology, Shenzhen 518055, China; Institute of Microbiology, Government College University Faisalabad, Pakistan.
School of Science, Shenzhen Key Laboratory of Flexible Printed Electronics Technology, Shenzhen Key Laboratory of Advanced Functional Carbon Materials Research and Comprehensive Application, Harbin Institute of Technology, Shenzhen 518055, China.
Drug Discov Today. 2024 Nov;29(11):104188. doi: 10.1016/j.drudis.2024.104188. Epub 2024 Sep 20.
Glioblastoma multiforme (GBM) is the most common CNS cancer, it has dismal survival rates despite several effective mediators: intensified cytotoxic therapy, chimeric antigen receptor (CAR)-T cell therapy, viral therapy, adoptive cell therapy, immune checkpoint blockade therapy, radiation therapy and vaccine therapy. This review examines the basic concepts underlying immune targeting and examines products such as checkpoint blockade drugs, CAR-T cells, oncolytic viruses, combinatory multimodal immunotherapy and cancer vaccines. New approaches to overcoming current constraints and challenges in GBM therapy are discussed, based on recent studies into these tactics, findings from ongoing clinical trials, as well as previous trial results.
多形性胶质母细胞瘤(GBM)是最常见的中枢神经系统癌症,尽管有几种有效的介质:强化细胞毒性疗法、嵌合抗原受体(CAR)-T 细胞疗法、病毒疗法、过继细胞疗法、免疫检查点阻断疗法、放射疗法和疫苗疗法,但它的生存率仍然很差。本综述检查了免疫靶向的基本概念,并检查了检查点阻断药物、CAR-T 细胞、溶瘤病毒、组合多模式免疫疗法和癌症疫苗等产品。根据这些策略的最新研究、正在进行的临床试验的结果以及以前的试验结果,讨论了克服 GBM 治疗当前限制和挑战的新方法。