Regine W F, Patchell R A, Strottmann J M, Meigooni A, Sanders M, Young B
Department of Radiation Medicine, University of Kentucky Medical Center, Lexington 40536-0293, USA.
J Neurosurg. 2000 Dec;93 Suppl 3:37-41. doi: 10.3171/jns.2000.93.supplement.
This investigation was performed to determine the tolerance and toxicities of split-course fractionated gamma knife radiosurgery (FSRS) given in combination with conventional external-beam radiation therapy (CEBRT).
Eighteen patients with previously unirradiated, gliomas treated between March 1995 and January 2000 form the substrate of this report. These included 11 patients with malignant gliomas, six with low-grade gliomas, and one with a recurrent glioma. They were stratified into three groups according to tumor volume (TV). Fifteen were treated using the initial FSRS dose schedule and form the subject of this report. Group A (four patients), had TV of 5 cm3 or less (7 Gy twice pre- and twice post-CEBRT); Group B (six patients), TV greater than 5 cm3 but less than or equal to 15 cm3 (7 Gy twice pre-CEBRT and once post-CEBRT); and Group C (five patients), TV greater than 15 cm3 but less than or equal to 30 cm3 (7 Gy once pre- and once post-CEBRT). All patients received CEBRT to 59.4 Gy in 1.8-Gy fractions. Dose escalation was planned, provided the level of toxicity was acceptable. All patients were able to complete CEBRT without interruption or experiencing disease progression. Unacceptable toxicity was observed in two Grade 4/Group B patients and two Grade 4/Group C patients. Eight patients required reoperation. In three (38%) there was necrosis without evidence of tumor. Neuroimaging studies were available for evaluation in 14 patients. Two had a partial (> or = 50%) reduction in volume and nine had a minor (> 20%) reduction in size. The median follow-up period was 15 months (range 9-60 months). Six patients remained alive for 3 to 60 months.
The imaging responses and the ability of these patients with intracranial gliomas to complete therapy without interruption or experiencing disease progression is encouraging. Excessive toxicity derived from combined FSRS and CEBRT treatment, as evaluated thus far in this study, was seen in patients with Group B and C lesions at the 7-Gy dose level. Evaluation of this novel treatment strategy with dose modification is ongoing.
本研究旨在确定分割疗程的伽玛刀放射外科(FSRS)联合传统外照射放疗(CEBRT)的耐受性和毒性。
1995年3月至2000年1月期间治疗的18例既往未接受过放疗的胶质瘤患者构成了本报告的研究对象。其中包括11例恶性胶质瘤患者、6例低级别胶质瘤患者和1例复发性胶质瘤患者。根据肿瘤体积(TV)将他们分为三组。15例患者采用初始FSRS剂量方案进行治疗,构成了本报告的研究对象。A组(4例患者),肿瘤体积为5 cm³或更小(CEBRT前后各两次,每次7 Gy);B组(6例患者),肿瘤体积大于5 cm³但小于或等于15 cm³(CEBRT前两次,每次7 Gy,CEBRT后一次);C组(5例患者),肿瘤体积大于15 cm³但小于或等于30 cm³(CEBRT前后各一次,每次7 Gy)。所有患者均接受CEBRT,总剂量为59.4 Gy,每次剂量为1.8 Gy。如果毒性水平可接受,则计划增加剂量。所有患者均能够完成CEBRT,且未出现中断或疾病进展。在2例4级/B组患者和2例4级/C组患者中观察到不可接受的毒性。8例患者需要再次手术。其中3例(38%)出现坏死,无肿瘤证据。14例患者可进行神经影像学检查以评估。2例患者肿瘤体积部分(≥50%)缩小,9例患者肿瘤大小轻度(>20%)缩小。中位随访期为15个月(范围9 - 60个月)。6例患者存活3至60个月。
这些颅内胶质瘤患者的影像学反应以及能够不间断完成治疗或未出现疾病进展的能力令人鼓舞。根据本研究目前的评估,在7 Gy剂量水平下,B组和C组病变患者出现了FSRS与CEBRT联合治疗导致的过度毒性。正在对这种采用剂量调整的新型治疗策略进行评估。