Gj. Wang et al., POSITRON EMISSION TOMOGRAPHY STUDY OF HUMAN PROSTATIC ADENOCARCINOMA USING C-11 PUTRESCINE, Nuclear medicine and biology, 21(1), 1994, pp. 77-82
To evaluate [1-C-11]putrescine ([C-11]PUT) as a potential tracer for i
maging and characterization of human prostatic adenocarcinoma, positro
n emission tomography (PET) was performed in eight patients and three
normal controls. In addition, four of the patients and the three norma
l controls also had a prostate scan with 2-deoxy-2-[F-18]fluoro-D-gluc
ose ((18)FDG). Three of the patients had undergone resection of the pr
ostate tumor and all of the patients except for one had bone metastasi
s. Carbon-11 rapidly accumulated in prostate, bone and rectum after in
jection of [C-11]PUT. Maximal uptake was achieved 5 min after injectio
n with minimal washout during the 50 min study period. The uptake of c
arbon-ii in the prostate of normal controls was significantly higher t
han that in the patients. However, three of the four patients scanned
for metastatic bone lesions showed higher uptake in bone metastasis th
an in normal bone. Quantitation of (18)FDG uptake in the prostate was
hindered by the high accumulation of activity in the urinary bladder.
[C-11]PUT does not appear to be a useful tracer for assessing prolifer
ation of human prostate adenocarcinoma. Its utility in the imaging of
other cancers with high polyamine concentration remains to be investig
ated.