Shirato H, Kamada T, Hida K, Koyanagi I, Iwasaki Y, Miyasaka K, Abe H
Department of Radiology, Hokkaido University School of Medicine, Sapporo, Japan.
Int J Radiat Oncol Biol Phys. 1995 Sep 30;33(2):323-8. doi: 10.1016/0360-3016(95)00179-3.
To determine the role of radiotherapy in the management of spinal cord gliomas.
Thirty-six patients with spinal cord glioma treated between 1979 and 1993 were examined. The patients had 13 astrocytic tumors (7 astrocytomas, 4 anaplastic astrocytomas, 2 glioblastomas), 22 ependymal tumors (18 ependymomas, 4 myxopapillary ependymomas), and 1 unclassified glioma. Fifteen of the patients were treated by surgery alone, but the remaining 21 patients also received postoperative radiotherapy. Total resection was performed on 1 astrocytoma and 13 ependymomas. In general, 40-50 Gy/16-20 fractions/4-5 weeks were given after parital resection, but no radiotherapy was given after total resection.
Actuarial survival was significantly better for patients with ependymal tumors than for those with astrocytic tumors (p = 0007), 5-year actuarial survival rates being 96% and 50% for patients with ependymal tumors and astrocytic tumors, respectively. For patients with ependymal tumors, there was no difference in motor function and survival between those with total resection and those with partial resection followed by radiotherapy. Actuarial 3-year survival was 80% for patients with astrocytomas and 40% for those with anaplastic astrocytomas plus glioblastomas. The difference in the degree of motor function between the patients treated with radiotherapy and those without radiotherapy was not statistically significant. One anaplastic astrocytoma and one glioblastoma patient have lived longer than 4 years after radical treatment including radiocordectomy, or irradiation using doses larger than the tolerance threshold of the spinal cord.
Postoperative conventional radiotherapy is indicated after less than total resection of low-grade ependymal tumors and astrocytomas but not after total resection of ependymomas. Radiocordectomy may be an option for certain cases with high-grade astrocytic tumors.
确定放射治疗在脊髓胶质瘤治疗中的作用。
对1979年至1993年间接受治疗的36例脊髓胶质瘤患者进行了检查。这些患者中有13例星形细胞瘤(7例星形细胞瘤、4例间变性星形细胞瘤、2例胶质母细胞瘤)、22例室管膜瘤(18例室管膜瘤、4例黏液乳头型室管膜瘤)和1例未分类的胶质瘤。15例患者仅接受了手术治疗,但其余21例患者还接受了术后放射治疗。1例星形细胞瘤和13例室管膜瘤进行了全切除。一般来说,部分切除术后给予40 - 50 Gy/16 - 20次分割/4 - 5周的放疗,但全切除术后未给予放疗。
室管膜瘤患者的精算生存率显著高于星形细胞瘤患者(p = 0.007),室管膜瘤患者和星形细胞瘤患者的5年精算生存率分别为96%和50%。对于室管膜瘤患者,全切除患者与部分切除后放疗患者的运动功能和生存率无差异。星形细胞瘤患者的3年精算生存率为80%,间变性星形细胞瘤加胶质母细胞瘤患者为40%。接受放疗和未接受放疗患者的运动功能程度差异无统计学意义。1例间变性星形细胞瘤和1例胶质母细胞瘤患者在包括脊髓切除术或使用高于脊髓耐受阈值剂量的照射等根治性治疗后存活超过4年。
低级别室管膜瘤和星形细胞瘤次全切除术后应进行术后常规放疗,但室管膜瘤全切除术后则无需放疗。对于某些高级别星形细胞瘤病例,脊髓切除术可能是一种选择。