More than 50% of cancers fail to respond to any individual treatment a
nd tumour follow-up after treatment plays a major role in routine ther
apy planning and pharmacological research. Today, MRS is the only tech
nological approach providing non-invasive access to tumour biochemistr
y. Ten years ago. expectations were raised concerning P-31 MRS as an e
xciting and promising technical approach to the study of tumours. Howe
ver the expectations have not always come to fruition. How close are w
e now to seeing routine P-31 NMR in clinical oncology? This review of
the 127 published papers shows spectroscopy results in more than 150 e
xperimental animal tumour models. These tumour/host/treatment systems
provide us with a useful basis to evaluate the current state of the ar
t, summarize the basic knowledge presently available, determine the ke
y points underlying the present disappointment of some clinical oncolo
gists and stimulate new basic research. The information collected conc
erns the discussion of the reliability of experimental models in oncol
ogy, the technical improvement of magnetic resonance technology and th
e monitoring of bioenergetic status, pH regulation and phospholipid me
tabolism in treated and untreated tumours. Recent advances (two-thirds
of the papers have been published in the last 5 years) seem to provid
e more optimistic perspectives than those generally accepted a few yea
rs ago in the depressing period following early pioneering work.