Neyns Bart, Sadones Jan, Chaskis Cristo, De Ridder Mark, Keyaerts Marleen, Veld Peter In't, Michotte Alex
Medische Oncologie, Oncologisch Centrum, Academisch Ziekenhuis Vrije Universiteit Brussel (AZ-VUB), Brussel, Belgium.
Acta Neurol Belg. 2005 Sep;105(3):137-43.
Low-grade gliomas (LGG) are a group of uncommon neuroglial tumors of the central nervous system. They are characterized by a grade I or II according to the WHO classification. Grade I tumors are non-invasive and amenable to surgical resection with curative intent. Diffuse infiltrating LGG (WHO grade II) are tumors with a highly variable prognosis. Curative resection can only rarely be achieved and progression is characterized by transformation into a high-grade glioma (WHO grade III-IV). There are only limited evidence-based treatment recommendations for the management of progressive LGG because of a lack of data from prospective randomized trials. Most often radiotherapy is offered to patients with symptomatic and/or progressive disease. Three randomized trials have failed to demonstrate a survival improvement with either early versus delayed radiation or with a higher dose of radiation. The potential role of chemotherapy for the treatment of LGG has only been addressed in phase II trials. The PCV-chemotherapy regimen is associated with considerable toxicity that limits its applicability. The results with temozolomide (TMZ) chemotherapy have been more promising. Patients with chemosensitive LGG as predicted by heterozygotic loss of chromosomal arms Ip and 19q or methylation of the promoter of the MGMT-gene in the genome of the glioma cells respond to TMZ. Radiotherapy will be compared to chemotherapy asfirst line treatment for LGG in two phase III studies that are planned for by the brain tumor group of the European Organization for Research and Treatment of Cancer (BTG-EORTC) and Radiation Therapy Oncology Group (RTOG).
低级别胶质瘤(LGG)是一组中枢神经系统罕见的神经胶质肿瘤。根据世界卫生组织(WHO)分类,它们被归类为I级或II级。I级肿瘤是非侵袭性的,可通过手术切除达到治愈目的。弥漫性浸润性LGG(WHO II级)是预后差异很大的肿瘤。很少能实现根治性切除,其进展表现为转变为高级别胶质瘤(WHO III-IV级)。由于缺乏前瞻性随机试验的数据,对于进展性LGG的管理,基于证据的治疗建议有限。大多数情况下,有症状和/或病情进展的患者会接受放疗。三项随机试验均未能证明早期放疗与延迟放疗或高剂量放疗相比能提高生存率。化疗在LGG治疗中的潜在作用仅在II期试验中得到探讨。PCV化疗方案具有相当大的毒性,限制了其应用。替莫唑胺(TMZ)化疗的结果更具前景。胶质瘤细胞基因组中染色体臂1p和19q杂合性缺失或MGMT基因启动子甲基化所预测的对TMZ敏感的LGG患者对TMZ有反应。在欧洲癌症研究与治疗组织(EORTC)脑肿瘤组和放射肿瘤学组(RTOG)计划开展的两项III期研究中,将对LGG的一线治疗放疗与化疗进行比较。