Journal article
Initial evaluation of 18F-fluorothymidine (FLT) PET/CT scanning for primary pancreatic cancer
European journal of nuclear medicine and molecular imaging, Vol.35(3), pp.527-531
03/2008
DOI: 10.1007/s00259-007-0630-z
PMCID: PMC4144989
PMID: 17960376
Abstract
Purpose
The aim of this study was to evaluate the potential of 18F-fluorothymidine (FLT) PET/CT for imaging pancreatic adenocarcinoma.
Methods
This was a pilot study of five patients (four males, one female) with newly diagnosed and previously untreated pancreatic adenocarcinoma. Patients underwent FLT PET/CT, 18F-fluorodeoxyglucose (FDG) PET/CT, and contrast-enhanced CT scanning before treatment. The presence of cancer was confirmed by histopathological analysis at the time of scanning in all five patients. The degree of FLT and FDG uptake at the primary tumor site was assessed using visual interpretation and semi-quantitative SUV analyses.
Results
The primary tumor size ranged from 2.5×2.8 cm to 3.5 × 7.0 cm. The SUV of FLT uptake within the primary tumor ranged from 2.1 to 3.1. Using visual interpretation, the primary cancer could be detected from background activity in two of five patients (40%) on FLT PET/CT. By comparison, FDG uptake was higher in each patient with a SUV range of 3.4 to 10.8, and the primary cancer could be detected from background in all five patients (100%).
Conclusions
In this pilot study of five patients with primary pancreatic adenocarcinoma, FLT PET/CT scanning showed poor lesion detectability and relatively low levels of radiotracer uptake in the primary tumor.
Details
- Title: Subtitle
- Initial evaluation of 18F-fluorothymidine (FLT) PET/CT scanning for primary pancreatic cancer
- Creators
- A Quon - Department of Radiology and Molecular Imaging Program at Stanford (MIPS), Stanford University Medical Center, 300 Pasteur Drive, Room H-0101, Stanford, CA 94305, USAS. T Chang - Department of Radiation Oncology, Stanford University Medical Center, 268 Campus Drive, Room 1245, Stanford, CA, USAF Chin - Department of Radiology and Molecular Imaging Program at Stanford (MIPS), Stanford University Medical Center, 300 Pasteur Drive, Room H-0101, Stanford, CA 94305, USAA Kamaya - Department of Radiology and Molecular Imaging Program at Stanford (MIPS), Stanford University Medical Center, 300 Pasteur Drive, Room H-0101, Stanford, CA 94305, USAD. W Dick - Department of Radiology and Molecular Imaging Program at Stanford (MIPS), Stanford University Medical Center, 300 Pasteur Drive, Room H-0101, Stanford, CA 94305, USAB. W Loo - Department of Radiation Oncology, Stanford University Medical Center, 268 Campus Drive, Room 1245, Stanford, CA, USAS. S Gambhir - Department of Radiology and Molecular Imaging Program at Stanford (MIPS), Stanford University Medical Center, 300 Pasteur Drive, Room H-0101, Stanford, CA 94305, USAA. C Koong - Department of Radiation Oncology, Stanford University Medical Center, 268 Campus Drive, Room 1245, Stanford, CA, USA
- Resource Type
- Journal article
- Publication Details
- European journal of nuclear medicine and molecular imaging, Vol.35(3), pp.527-531
- DOI
- 10.1007/s00259-007-0630-z
- PMID
- 17960376
- PMCID
- PMC4144989
- NLM abbreviation
- Eur J Nucl Med Mol Imaging
- ISSN
- 1619-7070
- eISSN
- 1619-7089
- Language
- English
- Date published
- 03/2008
- Academic Unit
- Radiology; Pharmaceutical Sciences and Experimental Therapeutics
- Record Identifier
- 9984051993802771
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