Blood flow–metabolic relationships are dependent on tumour size in non-small cell lung cancer: a study using quantitative contrast-enhanced computer tomography and positron emission tomography

Original Article

DOI: 10.1007/s00259-005-1932-7

Cite this article as:
Miles, K.A., Griffiths, M.R. & Keith, C.J. Eur J Nucl Med Mol Imaging (2006) 33: 22. doi:10.1007/s00259-005-1932-7

Abstract

Purpose

The purpose of this study was to undertake dual assessment of tumour blood flow and glucose metabolism in non-small cell lung cancer (NSCLC) using contrast-enhanced computed tomography (CE-CT) and 18F-fluorodeoxyglucose positron emission tomography (FDG-PET) in order to assess how the relationships between these parameters vary with tumour size and stage.

Methods

Tumour blood flow and glucose metabolism were assessed in 18 NSCLCs using quantitative CE-CT and FDG-PET respectively. Contrast enhancement and FDG uptake were both normalised to injected dose and patient weight to yield correspondingly the standardised perfusion value (SPV) and standardised uptake value (SUV). Tumour area was measured from conventional CT images.

Results

The ratio of SUV to SVP and the metabolic–flow difference (SUV–SVP) correlated with tumour size (r=0.56, p=0.015 and r=0.60 and p=0.008 respectively). A metabolic–flow difference of greater than 4 was more common amongst tumours of stages III and IV (odds ratio 10.5; 95% confidence limits 0.24–32.1). A significant correlation between SUV and SPV was found only for tumours smaller than 4.5 cm2 (r=0.85, p=0.03).

Conclusion

Blood flow–metabolic relationships are not consistent in NSCLC but depend upon tumour size and stage. Quantitative CE-CT as an adjunct to an FDG study undertaken using integrated PET-CT offers an efficient way to augment the assessment of tumour biology with possible future application as part of clinical care.

Keywords

Non-small cell lung cancer Tumour blood flow Glucose metabolism Tumour size 18F-FDG 

Copyright information

© Springer-Verlag 2005

Authors and Affiliations

  1. 1.Division of Clinical and Laboratory SciencesBrighton & Sussex Medical School, University of SussexBrightonUK
  2. 2.Queensland University of TechnologyBrisbaneAustralia
  3. 3.The Wesley Research InstituteBrisbaneAustralia

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