Tumour imaging is an essential part of the practice of oncology, with a cru
cial role in screening programmes and in diagnosis and staging of establish
ed disease. Furthermore, the assessment of tumour size by imaging, usually
with computer tomography (CT) scanning, is a key component in determining t
he tumour response to therapy both in clinical trials and in daily oncology
practice. Techniques such as CT, ultrasound (US) and magnetic resonance im
aging (MRI) provide high resolution anatomical images with detailed structu
ral information. However, these imaging modalities yield limited functional
information on the tumour tissues and often cannot distinguish residual di
sease from non-viable or necrotic tumour masses, nor can they detect minima
l residual disease. In contrast, radiopharmaceutical imaging and, in partic
ular, positron emission tomography (PET) can give some functional informati
on about the underlying tissues. The possibility of refining these techniqu
es and also the emergence of newer imaging modalities that call detect chan
ges in cancers at the physiological, cellular or molecular levels, gives ri
se to the notion that these methods will have implications for drug develop
ment strategies and also future clinical management. In this review, we bri
efly discuss the current role of imaging in clinical practice, describe som
e of the advances in imaging modalities currently undergoing evaluation, an
d speculate on the future role of these techniques in developmental therape
utics programmes. (C) 2000 Elsevier Science Ltd. All rights reserved.