Miwa Kazuhiro, Matsuo Masayuki, Ogawa Shin-ichi, Shinoda Jun, Yokoyama Kazutoshi, Yamada Jitsuhiro, Yano Hirohito, Iwama Toru
Chubu Medical Center for Prolonged Traumatic Brain Dysfunction, Kizawa Memorial Hospital, Minokamo, Gifu, Japan.
Radiat Oncol. 2014 Aug 14;9:181. doi: 10.1186/1748-717X-9-181.
This research paper presents a valid treatment strategy for recurrent glioblastoma multiforme (GBM) using hypofractionated stereotactic radiotherapy by intensity modulated radiation therapy (HS-IMRT) planned with 11C-methionine positron emission tomography (MET-PET)/computed tomography (CT)/magnetic resonance imaging (MRI) fusion.
Twenty-one patients with recurrent GBM received HS-IMRT planned by MET-PET/CT/MRI. The region of increased amino acid tracer uptake on MET-PET was defined as the gross tumor volume (GTV). The planning target volume encompassed the GTV by a 3-mm margin. Treatment was performed with a total dose of 25- to 35-Gy, given as 5- to 7-Gy daily for 5 days.
With a median follow-up of 12 months, median overall survival time (OS) was 11 months from the start of HS-IMRT, with a 6-month and 1-year survival rate of 71.4% and 38.1%, respectively. Karnofsky performance status was a significant prognostic factor of OS as tested by univariate and multivariate analysis. Re-operation rate was 4.8% for radiation necrosis. No other acute or late toxicity Grade 3 or higher was observed.
This is the first prospective study of biologic imaging optimized HS-IMRT in recurrent GBM. HS-IMRT with PET data seems to be well tolerated and resulted in a median survival time of 11 months after HS-IMRT.
本研究论文提出了一种针对复发性多形性胶质母细胞瘤(GBM)的有效治疗策略,即采用基于11C-蛋氨酸正电子发射断层扫描(MET-PET)/计算机断层扫描(CT)/磁共振成像(MRI)融合技术进行计划的大分割立体定向放射治疗(HS-IMRT)。
21例复发性GBM患者接受了由MET-PET/CT/MRI计划的HS-IMRT治疗。MET-PET上氨基酸示踪剂摄取增加的区域被定义为大体肿瘤体积(GTV)。计划靶体积在GTV周围外放3mm。治疗总剂量为25至35Gy,分5天给予,每天5至7Gy。
中位随访12个月,从HS-IMRT开始计算,中位总生存时间(OS)为11个月,6个月和1年生存率分别为71.4%和38.1%。经单因素和多因素分析,卡氏功能状态是OS的显著预后因素。放射性坏死的再次手术率为4.8%。未观察到其他3级或更高等级的急性或晚期毒性反应。
这是第一项关于复发性GBM中生物影像优化的HS-IMRT的前瞻性研究。基于PET数据的HS-IMRT似乎耐受性良好,HS-IMRT后的中位生存时间为11个月。