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幕上胶质瘤的放射治疗。821例研究。

Radiotherapy in supratentorial gliomas. A study of 821 cases.

作者信息

Heesters Mart, Molenaar Willemina, Go Gwan K

机构信息

Department of Radiotherapy, Groningen University Hospital, The Netherlands.

出版信息

Strahlenther Onkol. 2003 Sep;179(9):606-14. doi: 10.1007/s00066-003-1098-9.

Abstract

PURPOSE

Analysis of the results of radiotherapy in a large group of cerebral gliomas with identification of prognostic factors and the outcome with respect to different decades of treatment.

PATIENTS AND METHODS

Two decades (1979-1999) of radiotherapy in supratentorial astrocytic and oligodendroglial tumors (n = 821) at the University Hospital Groningen were retrospectively evaluated. Prognostic factors for survival were analyzed. Two decades of radiotherapy treatment were compared with respect to radiotherapy dose and treatment-field design.

RESULTS

Glioblastoma multiforme, including gliosarcoma, was the most frequent supratentorial glioma (n = 442) with a poor survival, i.e., median survival time (MST) 7 months, especially in patients > 50 years of age and with poor performance. Patients with good performance were selected for radiotherapy with an optimum dose of 60 Gy local-field irradiation. However, in patients with poor prognosis, no radiotherapy was applied or a shorter treatment scheme was given. Anaplastic astrocytomas (n = 131) were treated in the same way as glioblastoma multiforme. Over time, a decrease in radiation dose (from 60 to 45 Gy) and from whole brain irradiation to local-field treatment was observed, following the literature. In low-grade gliomas, prognostic factors for survival were age, performance, and extent of resection. Gemistocytic astrocytoma (n = 15) had an inferior survival compared to astrocytoma (MST 46 vs. 54 months), but a superior survival compared to anaplastic astrocytoma (MST 10 months). The presence of an oligodendroglial component in a glioma implied a superior survival compared to the astrocytic gliomas. The inherent biology of the glioma is reflected by the study of recurrent tumors with progression to higher grades of malignancy in 32-40% and by the histology of recurrent oligodendroglial tumors. In comparing two decades of radiotherapy in gliomas, no differences in survival were observed despite the technological improvements. However, reduction in long-term side effects was not evaluated, especially in low-grade gliomas which were treated in the second decade of the study with local fields only and a reduced radiotherapy dose using computerized three-dimensional (3-D) planning.

CONCLUSION

Radiotherapy does not cure cerebral glioma. Prognostic factors for survival are histopathologic classification and grading, age, and patient performance. Technological improvements do not improve survival, but possibly reduce late effects.

摘要

目的

分析一大组脑胶质瘤的放疗结果,确定预后因素以及不同治疗年代的治疗结局。

患者与方法

回顾性评估格罗宁根大学医院20年(1979 - 1999年)间幕上星形细胞瘤和少突胶质细胞瘤(n = 821例)的放疗情况。分析生存的预后因素。比较20年放疗在放疗剂量和治疗野设计方面的情况。

结果

多形性胶质母细胞瘤,包括胶质肉瘤,是最常见的幕上胶质瘤(n = 442例),生存率低,即中位生存时间(MST)为7个月,尤其是年龄>50岁且身体状况差的患者。身体状况良好的患者选择60 Gy局部野照射的最佳剂量进行放疗。然而,预后差的患者未进行放疗或给予较短的治疗方案。间变性星形细胞瘤(n = 131例)的治疗方式与多形性胶质母细胞瘤相同。随着时间推移,根据文献观察到放疗剂量从60 Gy降至45 Gy,且从全脑照射改为局部野治疗。在低级别胶质瘤中,生存的预后因素为年龄、身体状况和切除范围。胶质纤维状星形细胞瘤(n = 15例)的生存率低于星形细胞瘤(MST分别为46个月和54个月),但高于间变性星形细胞瘤(MST为10个月)。胶质瘤中存在少突胶质细胞成分意味着其生存率高于星形细胞胶质瘤。对复发性肿瘤的研究反映了胶质瘤的内在生物学特性,32% - 40%的复发性肿瘤会进展为更高等级的恶性肿瘤,以及复发性少突胶质细胞瘤组织学情况。在比较胶质瘤20年的放疗情况时,尽管技术有所改进,但未观察到生存率的差异。然而,未评估长期副作用的减少情况,尤其是在研究的第二个十年中仅采用局部野且使用计算机三维(3 - D)规划减少放疗剂量治疗的低级别胶质瘤。

结论

放疗不能治愈脑胶质瘤。生存的预后因素为组织病理学分类和分级、年龄及患者身体状况。技术改进并未提高生存率,但可能减少晚期效应。

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