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11C-Methionine positron emission tomography delineates non-contrast enhancing tumor regions at high risk for recurrence in pediatric high-grade glioma.
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.
Afiliación
  • Lucas JT; Department of Radiation Oncology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, MS 210, Memphis, TN, 38106-3678, USA. john.lucas@stjude.org.
  • Serrano N; Department of Radiation Oncology, Virginia Commonwealth University, Richmond, VA, USA.
  • Kim H; Department of Radiation Oncology, Thomas Jefferson University, Philadelphia, PA, USA.
  • Li X; Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Snyder SE; Department of Diagnostic Imaging, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Hwang S; Department of Diagnostic Imaging, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Li Y; Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Hua CH; Department of Radiation Oncology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, MS 210, Memphis, TN, 38106-3678, USA.
  • Broniscer A; Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Merchant TE; Department of Pediatrics, University of Tennessee Health Services Center, Memphis, TN, USA.
  • Shulkin BL; Department of Radiation Oncology, St. Jude Children's Research Hospital, 262 Danny Thomas Place, MS 210, Memphis, TN, 38106-3678, USA.
J Neurooncol ; 132(1): 163-170, 2017 03.
Article en En | MEDLINE | ID: mdl-28078638
ABSTRACT
We assessed the prognostic utility of 11C-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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Tomografía de Emisión de Positrones / Glioma Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Infant Idioma: En Revista: J Neurooncol Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Tomografía de Emisión de Positrones / Glioma Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Infant Idioma: En Revista: J Neurooncol Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos
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