Gannett D, Stea B, Lulu B, Adair T, Verdi C, Hamilton A
Department of Radiation Oncology, University of Arizona Health Sciences Center, Tucson 85724, USA.
Int J Radiat Oncol Biol Phys. 1995 Sep 30;33(2):461-8. doi: 10.1016/0360-3016(95)00087-F.
To evaluate the efficacy and toxicity of a stereotactic radiosurgery boost as part of the primary management of a minimally selected population of patients with malignant gliomas.
Between June, 1991 and January, 1994 a stereotactic radiosurgery boost was given to 30 patients after completion of fractionated external beam radiotherapy. The study population consisted of 22 males and 8 females, with a range in age at treatment from 5 to 74 years (median: 54 years). Tumor volume ranged from 2.1 to 115.5 cubic centimeters (cc) (median: 24 cc). Histology included 17 with glioblastoma multiforme, 10 with anaplastic astrocytoma, 1 with a mixed anaplastic astrocytoma-oligodendroglioma, and 2 with a gliosarcoma. A complete resection was performed in 9 (30%) patients, while 18 (60%) underwent a subtotal resection, and 3 (10%) received a biopsy only. Fractionated radiation dose ranged from 44 to 62 Gy, with a median of 59.4 Gy. Prescribed stereotactic radiosurgery dose ranged from 0.5 to 18 Gy (median: 10 Gy), and the volume receiving the prescription dose ranged from 2.1 to 158.7 cc (median: 46 cc). The volume of tumor receiving the prescription dose ranged from 70-100% (median: 100%). One to four (median: 2) isocenters were used, and collimator size ranged from 12.5 to 50 mm (median size: 32.5 mm). The median minimum stereotactic radiosurgery dose was 70% of the prescription dose and the median maximum dose was 200% of the prescription dose.
With a minimum follow-up of 1 year from radiosurgery, 7 (23%) of the patients are still living and 22 (73%) have died of progressive disease. One patient died of a myocardial infarction 5 months after stereotactic radiosurgery. Follow-up for living patients ranged from 12 to 45 months, with a median of 30 months. The 1- and 2-year disease-specific survival from the date of diagnosis is 57 [95% confidence interval (CI) 39 to 74%] and 25% (95% CI 9 to 41%), respectively (median survival: 13.9 months). No significant acute or late toxicity has been observed.
Stereotactic radiosurgery provides a safe and feasible technique for dose escalation in the primary management of unselected malignant gliomas. Longer follow-up and a randomized prospective trial is required to more thoroughly evaluate the role of radiosurgery in the primary management of malignant gliomas.
评估立体定向放射外科强化治疗作为恶性胶质瘤极少部分选定患者初始治疗一部分的疗效和毒性。
1991年6月至1994年1月期间,30例患者在完成分次外照射放疗后接受了立体定向放射外科强化治疗。研究人群包括22例男性和8例女性,治疗时年龄范围为5至74岁(中位数:54岁)。肿瘤体积范围为2.1至115.5立方厘米(cc)(中位数:24 cc)。组织学类型包括17例多形性胶质母细胞瘤、10例间变性星形细胞瘤、1例间变性星形细胞瘤-少突胶质细胞瘤混合型和2例胶质肉瘤。9例(30%)患者进行了全切,18例(60%)进行了次全切,3例(10%)仅接受了活检。分次放射剂量范围为44至62 Gy,中位数为59.4 Gy。规定的立体定向放射外科剂量范围为0.5至18 Gy(中位数:10 Gy),接受处方剂量的体积范围为2.1至158.7 cc(中位数:46 cc)。接受处方剂量的肿瘤体积范围为70 - 100%(中位数:100%)。使用了1至4个(中位数:2个)等中心,准直器尺寸范围为12.5至50 mm(中位尺寸:32.5 mm)。立体定向放射外科最小剂量中位数为处方剂量的70%,最大剂量中位数为处方剂量的200%。
自立体定向放射外科治疗后至少随访1年,7例(23%)患者仍存活,22例(73%)死于疾病进展。1例患者在立体定向放射外科治疗后5个月死于心肌梗死。存活患者的随访时间为12至45个月,中位数为30个月。自诊断之日起的1年和2年疾病特异性生存率分别为57%[95%置信区间(CI)39%至74%]和25%(95%CI 9%至41%)(中位生存期:13.9个月)。未观察到明显的急性或晚期毒性。
立体定向放射外科为未选定的恶性胶质瘤初始治疗中的剂量增加提供了一种安全可行的技术。需要更长时间的随访和随机前瞻性试验来更全面地评估放射外科在恶性胶质瘤初始治疗中的作用。