Division of Hematology and Oncology, Department of Internal Medicine, East Carolina University, Greenville, NC, USA.
Division of Neuro-Oncology, Department of Neurology, University of Virginia Neuro-Oncology Center, Box 800432, Charlottesville, VA, 22908-0432, USA.
Curr Treat Options Oncol. 2022 Sep;23(9):1219-1232. doi: 10.1007/s11864-022-01000-z. Epub 2022 Aug 1.
Treatment recommendations for grade 3 gliomas are guided by their histopathologic and molecular phenotype. In the 2021 WHO classification, these tumors are categorized into two types, grade 3 IDH mutant (IDHmt), 1p/19q codeleted oligodendroglioma and IDH mutant astrocytoma. Treatment consists of maximal safe surgery, followed by radiation therapy (RT) and alkylating agent-based chemotherapy. Based on the updated CATNON result, RT followed by temozolomide improves outcome in patients with non-codeleted grade 3 IDHmt astrocytoma. In patients with IDHmt, codeleted oligodendroglioma, the addition of procarbazine, CCNU, and vincristine regimen is the recommended treatment, based on large randomized controlled trials. These current treatments prolong the overall survival to up to 10 years in patients with grade 3 IDHmt astrocytoma and 14 years in grade 3 IDHmt codeleted oligodendroglioma. Treatment options at recurrence include re-resection, re-irradiation, and other cytotoxic chemotherapy; however, these are of limited benefit. Novel agents targeting IDH mutation and its metabolic effects are currently under investigation to improve the outcome of these patients.
治疗 3 级胶质瘤的建议取决于其组织病理学和分子表型。在 2021 年的世界卫生组织分类中,这些肿瘤分为两种类型,即 IDH 突变型(IDHmt)、1p/19q 共缺失少突胶质细胞瘤和 IDH 突变型星形细胞瘤。治疗包括最大限度的安全手术,随后进行放射治疗(RT)和烷化剂为基础的化疗。基于 CATNON 的最新结果,RT 后联合替莫唑胺可改善非共缺失 IDHmt 星形细胞瘤患者的预后。对于 IDHmt 共缺失少突胶质细胞瘤患者,根据大型随机对照试验,推荐使用洛莫司汀、卡莫司汀和长春新碱方案。这些当前的治疗方法将 IDHmt 星形细胞瘤患者的总生存期延长至 10 年,将 IDHmt 共缺失少突胶质细胞瘤患者的总生存期延长至 14 年。复发后的治疗选择包括再次切除、再次放疗和其他细胞毒性化疗,但这些治疗方法的获益有限。目前正在研究针对 IDH 突变及其代谢效应的新型药物,以改善这些患者的预后。