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[星形细胞瘤的个体化治疗以及显微手术、放疗和化疗的疗效]

[Individualized therapy and outcomes of microsurgery, radiotherapy, and chemotherapy for astrocytoma].

作者信息

Zhou Wang-Ning, Chen Zhong-Ping, You Chao, Mu Yong-Gao, Sai Ke, Zhang Jun-Ying, Zhang Xiang-Heng, Cheng Jin-Jian, Xu Hong-Chao

机构信息

Department of Neurosurgery, Cancer Center, Sun Yat-sen University, Guangzhou,Guangdong,510060, P.R.China.

出版信息

Ai Zheng. 2004 Nov;23(11 Suppl):1555-60.

Abstract

BACKGROUND & OBJECTIVE: Astrocytomas, constitute about 75% of neuroepithelial tumors, is one of the most common primary tumors in central nervous system with fairly high incidence and poor prognosis. Individualized multimodality is the hope for improving prognosis of patients with astrocytoma. This study was designed to investigate the efficiency of individualized treatment of microsurgery, radiotherapy, and chemotherapy for 62 patients with astrocytoma.

METHODS

Sixty-two patients with astrocytoma in study group were treated with individualized multimodality of microsurgery, postoperative radiotherapy, and/or postoperative chemotherapy according to in vitro sensitivity assay. After microsurgery, 59 patients accepted radiotherapy, 46 patients received chemotherapy. Fifty patients with astrocytoma in control group were treated with conventional treatment of surgery, chemotherapy, and radiotherapy. After surgery, 31 patients received radiotherapy following by BCNU chemotherapy, while 19 patients accepted BCNU chemotherapy following radiotherapy. Pathologic diagnosis of patients in study group were 19 cases of grade, 32 cases of grade III, and 11 cases of grade IV; in control group were 13 cases of grade II, 28 cases of grade III, and 9 cases of grade IV. Mean follow-up time were 25.8 months, and the outcome was evaluated by MRI, KPS, and survival rate.

RESULTS

Tumor total resection rate in study group was 67.7%, while that in control group was 58.0%. There was no significant difference of KPS and survival rate in patients with low-grade astrocytoma between 2 groups, while the outcome of patients with malignant astrocytoma was significantly improved by individualized treatment. In study group, 2-year expectant survival rate of patients with astrocytoma of grade III, and grade IV were 93.7%, and 36.3%, while in control group were 67.5%, and 22.2% (P< 0.05). In glioblastoma patients, median survival time of study group was 18.68 months, while that of control group was 12.83 months (P< 0.01).

CONCLUSION

Individualized microsurgery may improve the total resection of astrocytoma, and benefit to postoperative treatment.Individualized radiotherapy/chemotherapy may prevent patients from some complications. Individualized management may improve prognosis of patients with astrocytoma, particularly malignant astrocytoma.

摘要

背景与目的

星形细胞瘤约占神经上皮肿瘤的75%,是中枢神经系统最常见的原发性肿瘤之一,发病率较高且预后较差。个体化多模式治疗是改善星形细胞瘤患者预后的希望。本研究旨在探讨显微手术、放疗和化疗个体化治疗62例星形细胞瘤患者的疗效。

方法

研究组62例星形细胞瘤患者根据体外药敏试验采用显微手术、术后放疗和/或术后化疗的个体化多模式治疗。显微手术后,59例患者接受放疗,46例患者接受化疗。对照组50例星形细胞瘤患者采用手术、化疗和放疗的传统治疗方法。手术后,31例患者先接受放疗后行卡氮芥化疗,19例患者先接受放疗后行卡氮芥化疗。研究组患者病理诊断为Ⅱ级19例,Ⅲ级32例,Ⅳ级11例;对照组Ⅱ级13例,Ⅲ级28例,Ⅳ级9例。平均随访时间为25.8个月,通过磁共振成像(MRI)、卡氏功能状态评分(KPS)和生存率评估疗效。

结果

研究组肿瘤全切除率为67.7%,对照组为58.0%。两组低级别星形细胞瘤患者的KPS和生存率无显著差异,而个体化治疗显著改善了恶性星形细胞瘤患者的疗效。研究组Ⅲ级和Ⅳ级星形细胞瘤患者的2年预期生存率分别为93.7%和36.3%,而对照组分别为67.5%和22.2%(P<0.05)。在胶质母细胞瘤患者中,研究组的中位生存时间为18.68个月,而对照组为12.83个月(P<0.01)。

结论

个体化显微手术可提高星形细胞瘤的全切除率,并有利于术后治疗。个体化放疗/化疗可预防患者出现一些并发症。个体化治疗可改善星形细胞瘤患者,尤其是恶性星形细胞瘤患者的预后。

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