Sakata K, Hareyama M, Komae T, Shirato H, Watanabe O, Watarai J, Takai K, Yamada S, Tsuchida E, Sakai K
Department of Radiology, Sapporo Medical University, School of Medicine, Sapporo, Japan.
Jpn J Clin Oncol. 2001 Jun;31(6):240-5. doi: 10.1093/jjco/hye052.
There is at present no consensus on the policy for the treatment of patients with low-grade gliomas (LGGs).
This report is a retrospective multi-institutional study of 100 patients (ages 16-65 years) with astrocytoma (grade II), oligodendroglioma, anaplastic oligodendroglioma and anaplastic oligoastrocytoma of the supratentorial areas which were treated with surgery and postoperative radiotherapy at five university hospitals in northern Japan between 1990 and 1997 when MRI was routinely used to determine the target volume. Most patients were irradiated with 50-60 Gy. The target volume usually covered the areas with T2 prolongation of MRI with a margin of 2 cm.
The disease-specific 5-year survival rate was 87.4% for patients with oligodendroglioma and 75.3% for patients with astrocytoma. Survival for patients with astrocytoma in the MRI era appears to be improved compared with historical controls in the literature. Patients with astrocytoma aged 40 years and under had a significantly better disease-specific survival rate than those over 40 years (P < 0.05) and patients with oligodendroglioma and oligoastrocytoma showed a similar tendency. Patients with astrocytoma who had over 50% of their tumor removed had a significantly better survival rate than those who had less than 50% removed (P < 0.05). Chemotherapy appeared to improve the disease-specific survival rate of patients with oligodendroglioma but not that of patients with astrocytoma.
Oligodendroglioma has a more protracted course of disease progression than astrocytoma. This particular feature and the sensitivity of LGGs to chemotherapy as well as their relevant prognostic factors, such as age, histopathology and amount of tumor removal, should be taken into account before any decision on treatment methods for LGGs is made.
目前对于低级别胶质瘤(LGGs)患者的治疗策略尚无共识。
本报告是一项回顾性多机构研究,研究对象为100例年龄在16至65岁之间的幕上星形细胞瘤(二级)、少突胶质细胞瘤、间变性少突胶质细胞瘤和间变性少突星形细胞瘤患者,这些患者于1990年至1997年期间在日本北部的五所大学医院接受了手术及术后放疗,当时常规使用MRI来确定靶区体积。大多数患者接受了50 - 60 Gy的照射。靶区体积通常覆盖MRI上T2延长的区域,并外放2 cm的边界。
少突胶质细胞瘤患者的疾病特异性5年生存率为87.4%,星形细胞瘤患者为75.3%。与文献中的历史对照相比,MRI时代星形细胞瘤患者的生存率似乎有所提高。40岁及以下的星形细胞瘤患者的疾病特异性生存率显著高于40岁以上的患者(P < 0.05),少突胶质细胞瘤和少突星形细胞瘤患者也显示出类似趋势。肿瘤切除超过50%的星形细胞瘤患者的生存率显著高于切除少于50%的患者(P < 0.05)。化疗似乎提高了少突胶质细胞瘤患者的疾病特异性生存率,但对星形细胞瘤患者无效。
少突胶质细胞瘤疾病进展过程比星形细胞瘤更为缓慢。在对LGGs做出任何治疗方法的决策之前,应考虑到这一特殊特征以及LGGs对化疗的敏感性及其相关预后因素,如年龄、组织病理学和肿瘤切除量。