Measurement of clinical and subclinical tumour response using [F-18]-fluorodeoxyglucose and positron emission tomography: Review and 1999 EORTC recommendations
H. Young et al., Measurement of clinical and subclinical tumour response using [F-18]-fluorodeoxyglucose and positron emission tomography: Review and 1999 EORTC recommendations, EUR J CANC, 35(13), 1999, pp. 1773-1782
[F-18]-fluorodeoxyglucose ([F-18]-FDG) uptake is enhanced in most malignant
tumours which in turn can be measured using positron emission tomography (
PET). A number of small clinical trials have indicated that quantification
of the change in tumour [F-18]-FDG uptake may provide an early, sensitive,
pharmacodynamic marker of the tumoricidal effect of anticancer drugs. This
may allow for the introduction of subclinical response for anticancer drug
evaluation in early clinical trials and improvements in patient management.
For comparison of results from smaller clinical trials and larger-scale mu
lticentre trials a consensus is desirable for: (i) common measurement crite
ria; and (ii) reporting of alterations in [F-18]-FDG uptake with treatment.
This paper summarises the current status of the technique and recommendati
ons on the measurement of [F-18]-FDG uptake for tumour response monitoring
from a consensus meeting of the European Organization for Research and Trea
tment of Cancer (EORTC) PET study group held in Brussels in February 1998 a
nd confirmed at a subsequent meeting in March 1999. (C) 1999 Elsevier Scien
ce Ltd. All rights reserved.