A. Dimitrakopouloustrauss et al., FLUORINE-18-FLUOROURACIL TO PREDICT THERAPY RESPONSE IN LIVER METASTASES FROM COLORECTAL-CARCINOMA, The Journal of nuclear medicine, 39(7), 1998, pp. 1197-1202
Prediction of chemotherapy response is still a problem in oncological
patients. Methods: Studies with PET and F-18-fluorouracil (FU) were us
ed for measurements of drug concentrations in patients with liver meta
stases from colorectal carcinoma. The PET data obtained before onset o
f FU chemotherapy were correlated to the growth rate of the metastases
after therapy, The final evaluation included 25 metastases obtained i
n 17 patients, CT preceded the first chemotherapeutic cycle and was re
peated within 3-11 mo after onset of treatment. The uptake of the cyto
static agent was evaluated in the liver metastases using the SUV at 12
0 min after tracer infusion. Tumor growth rate of the metastases was c
alculated based on CT volumetric data. Results: The trapping of F-18-F
U was highly variable even for multiple metastases in the same patient
s. Six metastases with high F-18-FU uptake values exceeding 3.0 SUV co
rrelated with negative growth rate values, 5 of 25 metastases with int
ermediate uptake values ranging from 2.0-3.0 SUV were associated with
almost stable growth rate values nearly zero and 14 of 25 metastases w
ith low uptake values < 2.0 SUV demonstrated positive growth rate valu
es. Only metastases with a F-18-FU uptake exceeding 3.0 SUV at 120 min
postinjection demonstrated a response to therapy. A significant corre
lation of 0.86 (p < 0.001) was found between the F-18-FU uptake values
in the metastases measured before chemotherapy and the growth rate of
the lesions after treatment. Conclusion: The data show, that FU chemo
therapy outcome can be predicted using a single PET study with F-18-FU
before onset to therapy.