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伴或不伴术后放疗的少突胶质细胞瘤的治疗

Treatment of oligodendrogliomas with or without postoperative irradiation.

作者信息

Wallner K E, Gonzales M, Sheline G E

机构信息

Department of Radiation Oncology, University of California, San Francisco.

出版信息

J Neurosurg. 1988 May;68(5):684-8. doi: 10.3171/jns.1988.68.5.0684.

Abstract

The authors have reviewed the treatment results in 42 patients with intracranial oligodendroglioma treated from 1940 through 1983 at the University of California, San Francisco. Two patients who died postoperatively were excluded from analysis. Eleven patients had mixed tumors, with a minor astrocytic component. The overall survival rates for the 29 patients with pure oligodendroglioma were 61% and 33% at 5 and 10 years, respectively; these rates for the 11 patients with mixed tumors were 57% and 38% at 5 and 10 years, respectively. The 10-year survival rate for 14 patients with pure oligodendroglioma who received greater than 45 Gy irradiation was 56% versus 18% for 11 patients who did not receive postoperative irradiation (p = 0.09). Nine patients with mixed tumor who received more than 45 Gy postoperatively had survival rates similar to those for the 14 patients with pure tumors irradiated with more than 45 Gy (p = 0.89). All patients who died of their tumor had evidence of intracranial recurrence. One patient, who did not receive initial postoperative irradiation, also had clinical and myelographic evidence of spinal seeding. All five patients examined postmortem had tumor recurrence at the primary site; one patient also had intraventricular seeding. Six of the 10 patients with pure oligodendroglioma who had a repeat biopsy at the time of tumor recurrence or at postmortem examination showed histological progression to an anaplastic astrocytoma or glioblastoma multiforme. Based on this study, adult patients with pure or mixed oligodendroglioma currently are treated with partial-brain irradiation to a dose of about 60 Gy. In general, children are treated with partial-brain irradiation to about 50 Gy.

摘要

作者回顾了1940年至1983年在加利福尼亚大学旧金山分校接受治疗的42例颅内少突胶质细胞瘤患者的治疗结果。两名术后死亡的患者被排除在分析之外。11例患者为混合性肿瘤,伴有少量星形细胞成分。29例纯少突胶质细胞瘤患者的5年和10年总生存率分别为61%和33%;11例混合性肿瘤患者的5年和10年总生存率分别为57%和38%。14例接受超过45 Gy放疗的纯少突胶质细胞瘤患者的10年生存率为56%,而11例未接受术后放疗的患者为18%(p = 0.09)。9例术后接受超过45 Gy放疗的混合性肿瘤患者的生存率与14例接受超过45 Gy放疗的纯肿瘤患者相似(p = 0.89)。所有死于肿瘤的患者均有颅内复发证据。1例未接受初始术后放疗的患者也有临床和脊髓造影证据显示脊髓播散。所有5例尸检患者在原发部位均有肿瘤复发;1例患者还出现脑室内播散。10例纯少突胶质细胞瘤患者中有6例在肿瘤复发时或尸检时进行了重复活检,结果显示组织学进展为间变性星形细胞瘤或多形性胶质母细胞瘤。基于这项研究,目前纯少突胶质细胞瘤或混合性少突胶质细胞瘤的成年患者接受局部脑放疗,剂量约为60 Gy。一般来说,儿童接受局部脑放疗的剂量约为50 Gy。

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