Suppr超能文献

多形性胶质母细胞瘤的立体定向放射外科治疗

Stereotactic radiosurgery for glioblastoma multiforme.

作者信息

Masciopinto J E, Levin A B, Mehta M P, Rhode B S

机构信息

Department of Neurological Surgery, University of Wisconsin Hospitals and Clinics, Madison, USA.

出版信息

Stereotact Funct Neurosurg. 1994;63(1-4):233-40. doi: 10.1159/000100319.

Abstract

From February 1989 to August 1992, 26 patients who presented with an initial pathological diagnosis of glioblastoma multiforme underwent tumor debulking (17) or biopsy (9), stereotactic radiosurgery (SR) and standard radiation therapy (dose range 50-66 Gy) as part of their primary tumor therapy. Presenting characteristics included median age of 55 years (range 20-79), Karnofsky Performance Score (KPS) median 82.5 (20-100), and median tumor volume 18.6 cm3 (2.2-59.7). SR collimator size ranged from 2.25 to 4 cm with a central dose of 15-35 Gy. Isocenter location, collimator size and beam paths were individualized using three-dimensional software such that the maximum possible solid angle was subtended without exceeding a 20% tumor dose gradient. The mean follow-up was 10.9 months (6-19.5) with a median of 9.5 months. Statistical analysis was performed using Kaplan-Meier actuarial analysis developing predicted 12-month survival rates. There were no significant differences noted in patient survival for the parameters of biopsy versus debulking, single versus multiple isocenters, age, initial KPS, and patterns of steroid requirement. Radiographic recurrences were divided by location into central (within central SR dose) = 0, peripheral (within 1 cm of central dose) = 16, and distant (< 1 cm) = 4. Predicted 12-month survival was 24%, with a median survival of 9.5 months. These values are similar to previous results for surgery and standard radiotherapy alone [1]. The results suggest that radiosurgery, when used as a mode of primary therapy, offers little or no benefit in quality of life or survival as recurrences occur immediately outside or distant to the central SR field.

摘要

1989年2月至1992年8月期间,26例最初病理诊断为多形性胶质母细胞瘤的患者接受了肿瘤大部切除(17例)或活检(9例)、立体定向放射外科治疗(SR)和标准放射治疗(剂量范围50 - 66 Gy),作为其原发性肿瘤治疗的一部分。呈现的特征包括中位年龄55岁(范围20 - 79岁),卡氏功能状态评分(KPS)中位数82.5(20 - 100),以及中位肿瘤体积18.6 cm³(2.2 - 59.7)。SR准直器尺寸范围为2.25至4 cm,中心剂量为15 - 35 Gy。使用三维软件对等中心位置、准直器尺寸和射线路径进行个体化设置,以便在不超过20%肿瘤剂量梯度的情况下对最大可能的立体角进行对向照射。平均随访时间为10.9个月(6 - 19.5个月),中位数为9.5个月。使用Kaplan - Meier精算分析进行统计分析,得出预测的12个月生存率。在活检与大部切除、单一等中心与多个等中心、年龄、初始KPS以及类固醇需求模式等参数方面,患者生存率未发现显著差异。影像学复发按位置分为中心型(在中心SR剂量范围内)= 0例,周边型(在中心剂量1 cm范围内)= 16例,远处型(< 1 cm)= 4例。预测的12个月生存率为24%,中位生存期为9.5个月。这些值与之前单独进行手术和标准放疗的结果相似[1]。结果表明,当将放射外科作为主要治疗方式时,由于复发立即出现在中心SR野之外或远处,在生活质量或生存率方面几乎没有益处。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验