Lucas John T, Serrano Nick, Kim Hyun, Li Xingyu, Snyder Scott E, Hwang Scott, Li Yimei, Hua Chia-Ho, Broniscer Alberto, Merchant Thomas E, Shulkin Barry L
Department of Radiation Oncology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, MS 210, Memphis, TN, 38106-3678, USA.
Department of Radiation Oncology, Virginia Commonwealth University, Richmond, VA, USA.
J Neurooncol. 2017 Mar;132(1):163-170. doi: 10.1007/s11060-016-2354-z. Epub 2017 Jan 11.
We assessed the prognostic utility of C-Methionine positron emission tomography (MET-PET) in pediatric high-grade glioma (HGG). Thirty-one children had 62 MET-PET studies. Segmented tumor volumes from co-registered magnetic resonance studies were assessed for concordance with MET-PET uptake using Boolean operations. The tumor volume at diagnosis and treatment failure was assessed relative to MET-PET avid volume. The prognostic impact of MET-PET-delineated non-contrast enhancing tumor (NCET) was assessed. NCET was defined as the region of tumor defined by defined by FLAIR which did not enhance but showed MET-PET avidity. MET-PET concordance varied according to magnetic resonance sequence. MET-PET rarely added to the tumor volume in most cases. The volume of MET-PET with standardized uptake value >3.0 was differentially distributed at diagnosis, post treatment, and at recurrence. The initial MET-PET region overlapped with recurrent tumor in 90% of the cases. When the proportion of tumor which was NCET was >10%, an earlier time to progression (5.8 months; 95% CI, 1-8.2 vs. 10.5 months; 95% CI, 0.9-NR; p = 0.035) was noted. MET-PET delineates regions at increased risk for recurrence and may improve the definition of failure, prognostic assessment, and target definition for radiotherapy.
我们评估了¹¹C-蛋氨酸正电子发射断层扫描(MET-PET)在儿童高级别胶质瘤(HGG)中的预后效用。31名儿童接受了62次MET-PET检查。利用布尔运算评估来自配准磁共振研究的分割肿瘤体积与MET-PET摄取的一致性。相对于MET-PET摄取活跃体积评估诊断时和治疗失败时的肿瘤体积。评估MET-PET划定的非增强肿瘤(NCET)的预后影响。NCET定义为由液体衰减反转恢复序列(FLAIR)界定的未强化但显示MET-PET摄取活跃的肿瘤区域。MET-PET的一致性根据磁共振序列而有所不同。在大多数情况下,MET-PET很少增加肿瘤体积。标准化摄取值>3.0的MET-PET体积在诊断时、治疗后和复发时分布不同。90%的病例中,初始MET-PET区域与复发性肿瘤重叠。当肿瘤中NCET的比例>10%时,观察到进展时间更早(5.8个月;95%置信区间,1 - 8.2个月 vs. 10.5个月;95%置信区间,0.9 - 未报告;p = 0.035)。MET-PET划定复发风险增加的区域,可能改善失败的定义、预后评估以及放疗的靶区定义。