Currently it is difficult to predict the efficacy of any therapeutic m
odality in individual patients. If it could be shown that successful t
herapy causes some chemical alteration in the tumor before gross alter
ation in size becomes radiologically visible, the therapeutic regimen
could potentially be modified, sparing the patients longer trials of i
neffective therapy. We used proton nuclear magnetic resonance spectros
copy to detect the presence of simple metabolites (such as lactic acid
, creatine/phosphocreatine, N-acetyl aspartate, and the ''choline'' po
ol) in extracts of a human glioma grown subcutaneously in athymic (''n
u/nu'') mice. By comparing the tumor spectra obtained from untreated m
ice with tumor spectra from mice treated with chemotherapy or irradiat
ion, we have shown a significant decrease in the lactate/creatine and
lactate/choline values in tumors of similar size following treatment.
Such information could prove valuable as a means of monitoring tumor t
herapy when obtained noninvasively from spatially localized in vivo sp
ectra.