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放疗和化疗可改善少突胶质细胞瘤的预后。

Radiation and chemotherapy improve outcome in oligodendroglioma.

作者信息

Allison R R, Schulsinger A, Vongtama V, Barry T, Shin K H

机构信息

Roswell Park Cancer Institute, Buffalo, NY 14203, USA.

出版信息

Int J Radiat Oncol Biol Phys. 1997 Jan 15;37(2):399-403. doi: 10.1016/s0360-3016(96)00452-x.

Abstract

PURPOSE

Oligodendroglioma is a rare central nervous system tumor which may occur in pure or mixed histology. This scarcity results in difficulty in defining optimal management, mainly due to a lack of outcome analysis. Results are further complicated because the reported series include patients treated before megavoltage radiation or computed tomographic (CT) scan development. This makes extrapolation of outcome difficult to apply to modern-era patients. We report results obtained by current treatment and evaluation.

METHODS AND MATERIALS

Outcome of all 38 patients (age 5-70 years) pathologically diagnosed between 1975 and 1993 were reviewed. Pure lesions were seen in 14 cases, of which three were anaplastic. The remainder had mixed tumors, of which six contained anaplastic astrocytic elements. Each patient had undergone maximal debulking surgery, but all remained with residual disease on postoperative CT.

RESULTS

For nonanaplastic lesions, no local failure was seen in any patient receiving postoperative radiation (60 Gy) and chemotherapy (vincristine, procarbazine, and carmustine). Follow-up ranged from 28 to 240 months (median 125; N = 6). No postoperative therapy or chemotherapy alone resulted in local failure in all nine patients at risk [time to failure (TTF): 2-40 months; median 25]. Radiation alone in doses of 50 Gy at 2 Gy per day resulted in all six patients failing (TTF: 12-52 months; median 36). Achieving 60 Gy at 2 Gy a day allowed five of eight patients to remain disease free (disease-free survival: 24-160 months; median 66), with three failing at 26, 40, and 60 months. All lesions containing anaplastic elements underwent postoperative radiation therapy (60 Gy) and chemotherapy, with five of nine patients alive and well (median disease-free survival: 48 months; range 28-120).

CONCLUSION

The combination of radiation and chemotherapy increases local control of oligodendroglioma whether they contain pure, mixed, or anaplastic histology. Radiation alone may offer good local control as long as 60 Gy is delivered. Chemotherapy alone appears to delay TTF and may be useful for pediatric patients.

摘要

目的

少突胶质细胞瘤是一种罕见的中枢神经系统肿瘤,可表现为纯组织学类型或混合组织学类型。由于病例稀缺,缺乏预后分析,因此难以确定最佳治疗方案。此外,已报道的病例系列包括在兆伏放疗或计算机断层扫描(CT)技术出现之前接受治疗的患者,这使得结果更加复杂,难以将这些结果外推应用于现代患者。我们报告了当前治疗和评估所获得的结果。

方法和材料

回顾了1975年至1993年间病理诊断的38例患者(年龄5 - 70岁)的治疗结果。其中14例为纯少突胶质细胞瘤,3例为间变性少突胶质细胞瘤。其余为混合性肿瘤,其中6例含有间变性星形细胞成分。每位患者均接受了最大程度的肿瘤切除手术,但术后CT检查均显示有残留病灶。

结果

对于非间变性病变,接受术后放疗(60 Gy)和化疗(长春新碱、丙卡巴肼和卡莫司汀)的患者均未出现局部复发(随访时间28至240个月,中位时间125个月;N = 6)。9例有局部复发风险的患者中,未接受术后治疗或仅接受化疗的患者均出现了局部复发[复发时间(TTF):2至40个月;中位时间25个月]。每天2 Gy剂量、总剂量50 Gy的单纯放疗导致6例患者全部复发(TTF:12至52个月;中位时间36个月)。每天2 Gy剂量、总剂量达到60 Gy时,8例患者中有5例无疾病复发(无病生存期:24至160个月;中位时间66个月),3例分别在26、40和60个月时复发。所有含有间变性成分的肿瘤均接受了术后放疗(60 Gy)和化疗,9例患者中有5例存活且情况良好(无病生存期中位数:48个月;范围28至120个月)。

结论

放疗和化疗联合应用可提高少突胶质细胞瘤的局部控制率,无论其组织学类型为纯型、混合型还是间变性。只要放疗剂量达到60 Gy,单纯放疗也可提供良好的局部控制。单纯化疗似乎可延迟复发时间,对儿童患者可能有用。

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