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International Journal of Oncology
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Print ISSN: 1019-6439 Online ISSN: 1791-2423
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May 2005 Volume 26 Issue 5

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International Journal of Molecular Medicine

International Journal of Molecular Medicine

International Journal of Molecular Medicine is an international journal devoted to molecular mechanisms of human disease.

International Journal of Oncology

International Journal of Oncology

International Journal of Oncology is an international journal devoted to oncology research and cancer treatment.

Molecular Medicine Reports

Molecular Medicine Reports

Covers molecular medicine topics such as pharmacology, pathology, genetics, neuroscience, infectious diseases, molecular cardiology, and molecular surgery.

Oncology Reports

Oncology Reports

Oncology Reports is an international journal devoted to fundamental and applied research in Oncology.

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine

Experimental and Therapeutic Medicine is an international journal devoted to laboratory and clinical medicine.

Oncology Letters

Oncology Letters

Oncology Letters is an international journal devoted to Experimental and Clinical Oncology.

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Explores a wide range of biological and medical fields, including pharmacology, genetics, microbiology, neuroscience, and molecular cardiology.

Molecular and Clinical Oncology

Molecular and Clinical Oncology

International journal addressing all aspects of oncology research, from tumorigenesis and oncogenes to chemotherapy and metastasis.

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World Academy of Sciences Journal

Multidisciplinary open-access journal spanning biochemistry, genetics, neuroscience, environmental health, and synthetic biology.

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International Journal of Functional Nutrition

Open-access journal combining biochemistry, pharmacology, immunology, and genetics to advance health through functional nutrition.

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International Journal of Epigenetics

Publishes open-access research on using epigenetics to advance understanding and treatment of human disease.

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Article

Glucose metabolism in brain tumours can be estimated using [18F]2-fluorodeoxyglucose positron emission tomography and a population-derived input function scaled using a single arterialised venous blood sample

  • Authors:
    • C. S. Brock
    • H. Young
    • S. Osman
    • S. K. Luthra
    • T. Jones
    • P. M. Price
  • View Affiliations / Copyright

    Affiliations: Cancer Research UK PET Oncology Group, London, UK
  • Pages: 1377-1383
    |
    Published online on: May 1, 2005
       https://doi.org/10.3892/ijo.26.5.1377
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Abstract

The aim of this study was to assess simplified methods for deriving input functions for estimating glucose metabolism using 18F-FDG-PET. Nine glioma patients underwent paired 18F-FDG-PET scans as part of a phase II study and the data used to estimate the metabolic rate of glucose (MRGlu) using a population-derived input function (arterial data from 14 scans) scaled using a single arterial blood sample taken at 20 min. Paired studies were performed in four further glioma patients with stable disease at least four months following radiotherapy to determine whether scaling the population-derived input function using a 20-min arterialised venous or venous sample further simplified the method. The heated hand method was used to obtain arterialised venous blood that approximated arterial blood. In the 9 phase II glioma patients, there was a good, statistically significant correlation between the MRGlu values estimated using the individual arterial input functions and the single arterial sample scaled population-derived input functions (r2=0.88, p<0.001, n=36). Blood samples collected during three scans on two of the stable disease patients showed no significant difference between the arterialised venous and arterial plasma concentrations of 18F (p>0.1, n=15) when the degree of arterialisation of the blood was monitored and maintained using a thermocouple. A significant difference was found between the plasma arterial and venous levels of 18F. There was an excellent correlation between MRGlu estimated using an arterial input function and a population-derived input function scaled using a single arterialised venous blood sample (r2=0.98, n=12). The method was reproducible with less than 4.4% variation between repeat tumour scans. Therefore, a population-derived input function scaled using a single arterialised venous blood sample at 20 min can be used for estimating MRGlu using 18F-FDG PET in glioma patients.

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Copy and paste a formatted citation
Spandidos Publications style
Brock CS, Young H, Osman S, Luthra SK, Jones T and Price PM: Glucose metabolism in brain tumours can be estimated using [18F]2-fluorodeoxyglucose positron emission tomography and a population-derived input function scaled using a single arterialised venous blood sample. Int J Oncol 26: 1377-1383, 2005.
APA
Brock, C.S., Young, H., Osman, S., Luthra, S.K., Jones, T., & Price, P.M. (2005). Glucose metabolism in brain tumours can be estimated using [18F]2-fluorodeoxyglucose positron emission tomography and a population-derived input function scaled using a single arterialised venous blood sample. International Journal of Oncology, 26, 1377-1383. https://doi.org/10.3892/ijo.26.5.1377
MLA
Brock, C. S., Young, H., Osman, S., Luthra, S. K., Jones, T., Price, P. M."Glucose metabolism in brain tumours can be estimated using [18F]2-fluorodeoxyglucose positron emission tomography and a population-derived input function scaled using a single arterialised venous blood sample". International Journal of Oncology 26.5 (2005): 1377-1383.
Chicago
Brock, C. S., Young, H., Osman, S., Luthra, S. K., Jones, T., Price, P. M."Glucose metabolism in brain tumours can be estimated using [18F]2-fluorodeoxyglucose positron emission tomography and a population-derived input function scaled using a single arterialised venous blood sample". International Journal of Oncology 26, no. 5 (2005): 1377-1383. https://doi.org/10.3892/ijo.26.5.1377
Copy and paste a formatted citation
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Spandidos Publications style
Brock CS, Young H, Osman S, Luthra SK, Jones T and Price PM: Glucose metabolism in brain tumours can be estimated using [18F]2-fluorodeoxyglucose positron emission tomography and a population-derived input function scaled using a single arterialised venous blood sample. Int J Oncol 26: 1377-1383, 2005.
APA
Brock, C.S., Young, H., Osman, S., Luthra, S.K., Jones, T., & Price, P.M. (2005). Glucose metabolism in brain tumours can be estimated using [18F]2-fluorodeoxyglucose positron emission tomography and a population-derived input function scaled using a single arterialised venous blood sample. International Journal of Oncology, 26, 1377-1383. https://doi.org/10.3892/ijo.26.5.1377
MLA
Brock, C. S., Young, H., Osman, S., Luthra, S. K., Jones, T., Price, P. M."Glucose metabolism in brain tumours can be estimated using [18F]2-fluorodeoxyglucose positron emission tomography and a population-derived input function scaled using a single arterialised venous blood sample". International Journal of Oncology 26.5 (2005): 1377-1383.
Chicago
Brock, C. S., Young, H., Osman, S., Luthra, S. K., Jones, T., Price, P. M."Glucose metabolism in brain tumours can be estimated using [18F]2-fluorodeoxyglucose positron emission tomography and a population-derived input function scaled using a single arterialised venous blood sample". International Journal of Oncology 26, no. 5 (2005): 1377-1383. https://doi.org/10.3892/ijo.26.5.1377
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