Department of Neurosurgery, Xiangya Hospital, Central South University, Changsha, China.
Xiangya School of Medicine, Central South University, Changsha, China.
Mol Cancer. 2022 Feb 8;21(1):39. doi: 10.1186/s12943-022-01513-z.
Gliomas are the common type of brain tumors originating from glial cells. Epidemiologically, gliomas occur among all ages, more often seen in adults, which males are more susceptible than females. According to the fifth edition of the WHO Classification of Tumors of the Central Nervous System (WHO CNS5), standard of care and prognosis of gliomas can be dramatically different. Generally, circumscribed gliomas are usually benign and recommended to early complete resection, with chemotherapy if necessary. Diffuse gliomas and other high-grade gliomas according to their molecule subtype are slightly intractable, with necessity of chemotherapy. However, for glioblastoma, feasible resection followed by radiotherapy plus temozolomide chemotherapy define the current standard of care. Here, we discuss novel feasible or potential targets for treatment of gliomas, especially IDH-wild type glioblastoma. Classic targets such as the p53 and retinoblastoma (RB) pathway and epidermal growth factor receptor (EGFR) gene alteration have met failure due to complex regulatory network. There is ever-increasing interest in immunotherapy (immune checkpoint molecule, tumor associated macrophage, dendritic cell vaccine, CAR-T), tumor microenvironment, and combination of several efficacious methods. With many targeted therapy options emerging, biomarkers guiding the prescription of a particular targeted therapy are also attractive. More pre-clinical and clinical trials are urgently needed to explore and evaluate the feasibility of targeted therapy with the corresponding biomarkers for effective personalized treatment options.
神经胶质瘤是源自神经胶质细胞的常见脑肿瘤类型。从流行病学角度来看,神经胶质瘤可发生于各个年龄段,多见于成年人,男性比女性更易患病。根据世界卫生组织(WHO)中枢神经系统肿瘤分类第五版(WHO CNS5),神经胶质瘤的标准治疗方法和预后可能存在显著差异。一般来说,局限性神经胶质瘤通常为良性,建议早期行完全切除术,如果有必要,还可进行化疗。弥漫性神经胶质瘤和其他高级别神经胶质瘤根据其分子亚型略有难治性,需要进行化疗。然而,对于胶质母细胞瘤,可行的切除后再加上放疗加替莫唑胺化疗是目前的标准治疗方法。在这里,我们讨论了治疗神经胶质瘤,特别是 IDH 野生型胶质母细胞瘤的新的可行或潜在靶点。由于复杂的调控网络,经典靶点如 p53 和视网膜母细胞瘤(RB)通路和表皮生长因子受体(EGFR)基因改变已经失败。免疫疗法(免疫检查点分子、肿瘤相关巨噬细胞、树突状细胞疫苗、CAR-T)、肿瘤微环境以及几种有效方法的联合治疗越来越受到关注。随着越来越多的靶向治疗选择的出现,指导特定靶向治疗处方的生物标志物也很有吸引力。迫切需要更多的临床前和临床试验来探索和评估靶向治疗的可行性及其相应的生物标志物,以实现有效的个体化治疗方案。