Mehta M P, Masciopinto J, Rozental J, Levin A, Chappell R, Bastin K, Miles J, Turski P, Kubsad S, Mackie T
Department of Human Oncology, University of Wisconsin Hospital and Clinics, Madison 53792.
Int J Radiat Oncol Biol Phys. 1994 Oct 15;30(3):541-9. doi: 10.1016/0360-3016(92)90939-f.
Prospective evaluation of the toxicity and efficacy of radiosurgery with external beam radiotherapy in the management of newly diagnosed glioblastoma.
From 5/89 to 12/92, 31 out of 51 patients with glioblastoma multiforme underwent radiosurgery, in addition to 54 Gy in 1.8 Gy/fraction following biopsy (n = 12) or resection (n = 19). Eligibility required supratentorial glioblastoma, tumor not > 4 cm in > 1 axis, age > 18 years, and location > 1 cm from optic chiasm. Patient characteristics were: age 20-78 years (median = 57); 22 male, 9 female; Karnofsky score 20-90 (m = 70), and volume of 2.3-59.7 c.c. (m = 17.4). Eighteen patients were treated with 1 collimator, 5 with 2, 7 with 3, and 1 with 4; peripheral isodoses were 40-90% (m = 72.5) and minimum and maximum tumor dose ranges were 10-20 (m = 12) and 15-35 Gy (m = 18.75). Patients were followed clinically and radiographically every 8-12 weeks to analyze survival, quality of life, and toxicity.
With a follow-up of 12-171 weeks, 8 out of 31 (26%) patients are alive. Median survival is 42 weeks. Twelve and 24-month actuarial survival are 38 and 28%. Comparison of the 2-year survival with previous Radiation Therapy Oncology Group patients was carried out using a nonparametric recursive partitioning technique and the observed vs. expected values are 28 vs. 9.7% (p < 0.05). Extent of resection and performance status were associated with improved survival in a multivariate analysis. No significant acute toxicity was encountered. Four patients (13%) developed clinically significant necrosis verified by biopsy or positron emission tomography scan at 9-59 weeks after radiosurgery.
The improvement in median survival in broadly selected glioblastoma patients treated with radiosurgery is difficult to determine, but the 2-year survival may be superior. Future randomized trials of radiosurgery are recommended, and ad hoc use of this modality should be discouraged.
前瞻性评估立体定向放射外科联合外照射放疗在新诊断胶质母细胞瘤治疗中的毒性和疗效。
从1989年5月至1992年12月,51例多形性胶质母细胞瘤患者中有31例接受了立体定向放射外科治疗,此外,活检(n = 12)或切除(n = 19)后接受了54 Gy、每次分割剂量1.8 Gy的放疗。入选标准为幕上胶质母细胞瘤、肿瘤在任一轴向上不大于4 cm、年龄大于18岁、肿瘤位置距视交叉大于1 cm。患者特征为:年龄20 - 78岁(中位数 = 57岁);男性22例,女性9例;卡氏评分20 - 90分(中位数 = 70分),体积2.3 - 59.7立方厘米(中位数 = 17.4立方厘米)。18例患者使用1个准直器治疗,5例使用2个,7例使用3个,1例使用4个;周边等剂量线为40 - 90%(中位数 = 72.5%),肿瘤最小和最大剂量范围分别为10 - 20 Gy(中位数 = 12 Gy)和15 - 35 Gy(中位数 = 18.75 Gy)。每8 - 12周对患者进行临床和影像学随访,以分析生存情况、生活质量和毒性。
随访12 - 171周,31例患者中有8例(26%)存活。中位生存期为42周。12个月和24个月的精算生存率分别为38%和28%。使用非参数递归分割技术将2年生存率与先前放射治疗肿瘤学组的患者进行比较,观察值与预期值分别为28%和9.7%(p < 0.05)。多因素分析显示,切除范围和功能状态与生存率提高相关。未出现明显的急性毒性。4例患者(13%)在立体定向放射外科治疗后9 - 59周经活检或正电子发射断层扫描证实发生了具有临床意义的坏死。
在广泛选择的接受立体定向放射外科治疗的胶质母细胞瘤患者中,中位生存期的改善难以确定,但2年生存率可能更高。建议未来进行立体定向放射外科的随机试验,不鼓励临时使用这种治疗方式。