Gj. Cook et al., DETECTION OF BONE METASTASES IN BREAST-CANCER BY (18)FDG PET - DIFFERING METABOLIC-ACTIVITY IN OSTEOBLASTIC AND OSTEOLYTIC LESIONS, Journal of clinical oncology, 16(10), 1998, pp. 3375-3379
Purpose: (99m)Technetium methylene diphosphonate (Tc-99m MDP) bone sci
ntigraphy is currently the method of choice for the detection of bone
metastases, but F-18-fluoro-deoxy-D-glucose positron emission tomograp
hy ((18)FDG PET) offers superior spatial resolution and improved sensi
tivity. We have compared (18)FDG PET with Tc-99m MDP bone scintigraphy
in patients with skeletal metastases from breast cancer and have anal
yzed the data in subgroups based on radiographic characteristics of le
sions. Patients and Methods: Twenty-three women with breast cancer and
confirmed bone metastases were studied with both 99mTc MDP bone scint
igraphy and (18)FDG PET, and the number of lesions detected and the qu
antitation of uptake (standardised uptake values [SUVs]) of (18)FDG in
osteolytic and osteoblastic metastases were compared. Survival was co
mpared for both lytic and blastic bone metastases and for patients wit
h high and low accumulation of (18)FDG. Results: (18)FDG PET detected
more lesions than Tc-99m MDP scintigraphy (mean, 14.1 and 7.8 lesions,
respectively; P < .01). However, (18)FDG detected fewer bone metastas
es compared with 99mTc MDP scintigraphy in a subgroup of patients with
osteoblastic disease (P < .05). Higher SUVs were observed for osteoly
tic than osteoblastic disease (mean, 6.77 and 0.95, respectively; P <
.01). Survival was lower in patients with osteolytic disease compared
with the remainder (P = .01). A difference in survival was not found f
or those patients with high SUVs (> 3.6; P = .4). Conclusion: (18)FDG
PET is superior to bone scintigraphy in the detection of osteolytic br
east cancer metastases, which led to a poorer prognosis. In contrast,
osteoblastic metastases show lower metabolic activity and are frequent
ly undetectable by PET. The biologic explanation for this observation
remains ta be elucidated. (C) 1998 by American Society of Clinical Onc
ology.