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6 - FDG-PET and PET/CT in Esophageal Cancer

Published online by Cambridge University Press:  08 August 2009

By
Sheila C. Rankin
Edited by
Sheila C. Rankin
Sheila C. Rankin
Affiliation:
Consultant Radiologist, Guy's and St. Thomas' Foundation Trust, London, UK
Sheila C. Rankin
Affiliation:
Guy's and St Thomas' Hospital
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Summary

Introduction

The anatomical imaging techniques of computer tomography (CT) and endoscopic ultrasound (EUS) have limitations in the staging of esophageal cancer, in assessing response to therapy, and in predicting survival. Functional imaging using positron emission tomography (PET) has been shown to provide unique information in other tumors and is increasingly being used in oesophageal cancer.

Positron emission tomography

PET is an imaging technique that can map functional activity before structural changes have taken place and has established a recognized place in imaging cancer. The most commonly used isotope at the present time is 18F-fluoro-2-deoxy-d-glucose (FDG), which can differentiate malignant from normal tissue based on the enhanced glucose transport and glycolysis exhibited by many tumor cells. FDG is a glucose analogue, and both FDG and glucose are taken up by cells via the membrane glucose transporter system and are phosphorylated by hexokinase. Unlike glucose, FDG-6-phosphate does not cross the cell membrane and is trapped in cells and is visualized. It can be dephosphorylated, but this is a slow process particularly in cancer cells that lack or have reduced levels of glucose-6-phosphatase. FDG accumulation depends on the rate of transport through the cell membrane that is mediated by glucose transporters (GLUT). Many malignant cells, including gastrointestinal tumors, show increased expression of GLUT-1, contributing to increased FDG accumulation, and this correlates with tumor invasiveness and poor survival in some cancers.

Type
Chapter
Information
Carcinoma of the Esophagus , pp. 85 - 106
Publisher: Cambridge University Press
Print publication year: 2007

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