Cargando…
A Pilot Study of 18F-FLT PET/CT in Pediatric Lymphoma
We performed an observational pilot study of 18F-FLT PET/CT in pediatric lymphoma. Eight patients with equivocal 18F-FDG PET/CT underwent imaging with 18F-FLT PET/CT. No immediate adverse reactions to 18F-FLT were observed. Compared to 18F-FDG, 18F-FLT uptake was significantly higher in bone marrow...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899586/ https://www.ncbi.nlm.nih.gov/pubmed/27313888 http://dx.doi.org/10.1155/2016/6045894 |
_version_ | 1782436488071348224 |
---|---|
author | Costantini, Danny L. Vali, Reza McQuattie, Susan Chan, Jeffrey Punnett, Angela Weitzman, Shiela Shammas, Amer Charron, Martin |
author_facet | Costantini, Danny L. Vali, Reza McQuattie, Susan Chan, Jeffrey Punnett, Angela Weitzman, Shiela Shammas, Amer Charron, Martin |
author_sort | Costantini, Danny L. |
collection | PubMed |
description | We performed an observational pilot study of 18F-FLT PET/CT in pediatric lymphoma. Eight patients with equivocal 18F-FDG PET/CT underwent imaging with 18F-FLT PET/CT. No immediate adverse reactions to 18F-FLT were observed. Compared to 18F-FDG, 18F-FLT uptake was significantly higher in bone marrow and liver (18F-FLT SUV 8.6 ± 0.6 and 5.0 ± 0.3, versus 18F-FDG SUV 1.9 ± 0.1 and 3.4 ± 0.7, resp., p < 0.05). In total, 15 lesions were evaluated with average 18F-FDG and 18F-FLT SUVs of 2.6 ± 0.1 and 2.0 ± 0.4, respectively. Nonspecific uptake in reactive lymph nodes and thymus was observed. Future studies to assess the clinical utility of 18F-FLT PET/CT in pediatric lymphoma are planned. |
format | Online Article Text |
id | pubmed-4899586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-48995862016-06-16 A Pilot Study of 18F-FLT PET/CT in Pediatric Lymphoma Costantini, Danny L. Vali, Reza McQuattie, Susan Chan, Jeffrey Punnett, Angela Weitzman, Shiela Shammas, Amer Charron, Martin Int J Mol Imaging Research Article We performed an observational pilot study of 18F-FLT PET/CT in pediatric lymphoma. Eight patients with equivocal 18F-FDG PET/CT underwent imaging with 18F-FLT PET/CT. No immediate adverse reactions to 18F-FLT were observed. Compared to 18F-FDG, 18F-FLT uptake was significantly higher in bone marrow and liver (18F-FLT SUV 8.6 ± 0.6 and 5.0 ± 0.3, versus 18F-FDG SUV 1.9 ± 0.1 and 3.4 ± 0.7, resp., p < 0.05). In total, 15 lesions were evaluated with average 18F-FDG and 18F-FLT SUVs of 2.6 ± 0.1 and 2.0 ± 0.4, respectively. Nonspecific uptake in reactive lymph nodes and thymus was observed. Future studies to assess the clinical utility of 18F-FLT PET/CT in pediatric lymphoma are planned. Hindawi Publishing Corporation 2016 2016-05-26 /pmc/articles/PMC4899586/ /pubmed/27313888 http://dx.doi.org/10.1155/2016/6045894 Text en Copyright © 2016 Danny L. Costantini et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Costantini, Danny L. Vali, Reza McQuattie, Susan Chan, Jeffrey Punnett, Angela Weitzman, Shiela Shammas, Amer Charron, Martin A Pilot Study of 18F-FLT PET/CT in Pediatric Lymphoma |
title | A Pilot Study of 18F-FLT PET/CT in Pediatric Lymphoma |
title_full | A Pilot Study of 18F-FLT PET/CT in Pediatric Lymphoma |
title_fullStr | A Pilot Study of 18F-FLT PET/CT in Pediatric Lymphoma |
title_full_unstemmed | A Pilot Study of 18F-FLT PET/CT in Pediatric Lymphoma |
title_short | A Pilot Study of 18F-FLT PET/CT in Pediatric Lymphoma |
title_sort | pilot study of 18f-flt pet/ct in pediatric lymphoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899586/ https://www.ncbi.nlm.nih.gov/pubmed/27313888 http://dx.doi.org/10.1155/2016/6045894 |
work_keys_str_mv | AT costantinidannyl apilotstudyof18ffltpetctinpediatriclymphoma AT valireza apilotstudyof18ffltpetctinpediatriclymphoma AT mcquattiesusan apilotstudyof18ffltpetctinpediatriclymphoma AT chanjeffrey apilotstudyof18ffltpetctinpediatriclymphoma AT punnettangela apilotstudyof18ffltpetctinpediatriclymphoma AT weitzmanshiela apilotstudyof18ffltpetctinpediatriclymphoma AT shammasamer apilotstudyof18ffltpetctinpediatriclymphoma AT charronmartin apilotstudyof18ffltpetctinpediatriclymphoma AT costantinidannyl pilotstudyof18ffltpetctinpediatriclymphoma AT valireza pilotstudyof18ffltpetctinpediatriclymphoma AT mcquattiesusan pilotstudyof18ffltpetctinpediatriclymphoma AT chanjeffrey pilotstudyof18ffltpetctinpediatriclymphoma AT punnettangela pilotstudyof18ffltpetctinpediatriclymphoma AT weitzmanshiela pilotstudyof18ffltpetctinpediatriclymphoma AT shammasamer pilotstudyof18ffltpetctinpediatriclymphoma AT charronmartin pilotstudyof18ffltpetctinpediatriclymphoma |