11C-Methionine positron emission tomography delineates non-contrast enhancing tumor regions at high risk for recurrence in pediatric high-grade glioma

被引:18
作者
Lucas, John T., Jr. [1 ]
Serrano, Nick [5 ]
Kim, Hyun [6 ]
Li, Xingyu [2 ]
Snyder, Scott E. [4 ]
Hwang, Scott [4 ]
Li, Yimei [2 ]
Hua, Chia-Ho [1 ]
Broniscer, Alberto [3 ,7 ]
Merchant, Thomas E. [1 ]
Shulkin, Barry L. [4 ]
机构
[1] St Jude Childrens Res Hosp, Dept Radiat Oncol, 262 Danny Thomas Pl,MS 210, Memphis, TN 38106 USA
[2] St Jude Childrens Res Hosp, Dept Biostat, 332 N Lauderdale St, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Oncol, 332 N Lauderdale St, Memphis, TN 38105 USA
[4] St Jude Childrens Res Hosp, Dept Diagnost Imaging, 332 N Lauderdale St, Memphis, TN 38105 USA
[5] Virginia Commonwealth Univ, Dept Radiat Oncol, Richmond, VA USA
[6] Thomas Jefferson Univ, Dept Radiat Oncol, Philadelphia, PA 19107 USA
[7] Univ Tennessee, Hlth Serv Ctr, Dept Pediat, Memphis, TN USA
关键词
MET-PET; Pediatric; High-grade glioma; GUIDED STEREOTACTIC BIOPSY; CONCURRENT TEMOZOLOMIDE; BRAIN-TUMORS; GLIOBLASTOMA; PET; METHIONINE; RADIATION; MRI;
D O I
10.1007/s11060-016-2354-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We assessed the prognostic utility of C-11-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.
引用
收藏
页码:163 / 170
页数:8
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