Kobayashi S, Takakura K
Gan To Kagaku Ryoho. 1986 Jan;13(1):11-7.
The histological classification, pathophysiology, and treatment modalities of malignant gliomas (glioblastoma, malignant astrocytoma) were reviewed with reference to the WHO classification of primary brain tumors and the recent progress made in glioma biology. Patients with glioblastoma and malignant astrocytoma showed, respectively, 10.6% and 22.2 of the five-year survival rate according to the All Japan Brain Tumor Registry. In order to improve the prognosis of malignant glioma patients, many clinical trials have been conducted throughout the world. Malignant gliomas that grow in and invade the brain parenchyma cannot be cured by surgical resection. One should treat the residual tumor with irradiation, chemotherapy and immunotherapy. Radiation therapy alone and radiation therapy plus chemotherapy using nitrosoureas or procarbazine have been proved statistically to be more effective for malignant gliomas than supportive care and radiation therapy alone, respectively. Prospective clinical trials support the view that malignant gliomas should be treated vigorously using a multimodal approach that includes surgical resection, high-dose radiation therapy, and prolonged maintenance chemotherapy.
参照世界卫生组织(WHO)原发性脑肿瘤分类以及胶质瘤生物学的最新进展,对恶性胶质瘤(胶质母细胞瘤、恶性星形细胞瘤)的组织学分类、病理生理学及治疗方式进行了综述。根据全日本脑肿瘤登记处的数据,胶质母细胞瘤和恶性星形细胞瘤患者的五年生存率分别为10.6%和22.2%。为改善恶性胶质瘤患者的预后,世界各地开展了许多临床试验。生长于脑实质并侵犯脑实质的恶性胶质瘤无法通过手术切除治愈。应采用放疗、化疗和免疫疗法治疗残留肿瘤。统计学证明,单纯放疗以及使用亚硝基脲类或丙卡巴肼的放疗加化疗,分别比单纯支持治疗和单纯放疗对恶性胶质瘤更有效。前瞻性临床试验支持这样的观点,即恶性胶质瘤应采用包括手术切除、高剂量放疗和延长维持化疗的多模式方法积极治疗。