Journal of Clinical Oncology, Vol 16, 3375-3379, Copyright © 1998 by American Society of Clinical Oncology
Detection of bone metastases in breast cancer by 18FDG PET: differing metabolic activity in osteoblastic and osteolytic lesions
GJ Cook, S Houston, R Rubens, MN Maisey and I Fogelman
Clinical Positron Emission Tomography Centre and Department of Oncology, Guys Hospital, United Medical and Dental Schools, London, United Kingdom. g.cook@umds.ac.uk
PURPOSE: 99mTechnetium methylene diphosphonate (99mTc MDP) bone
scintigraphy is currently the method of choice for the detection of bone
metastases, but 18F-fluoro-deoxy-D-glucose positron emission tomography
(18FDG PET) offers superior spatial resolution and improved sensitivity. We
have compared 18FDG PET with 99mTc MDP bone scintigraphy in patients with
skeletal metastases from breast cancer and have analyzed the data in
subgroups based on radiographic characteristics of lesions. PATIENTS AND
METHODS: Twenty-three women with breast cancer and confirmed bone
metastases were studied with both 99mTC MDP bone scintigraphy and 18FDG
PET, and the number of lesions detected and the quantitation of uptake
(standardized uptake values [SUVs]) of 18FDG in osteolytic and osteoblastic
metastases were compared. Survival was compared for both lytic and blastic
bone metastases and for patients with high and low accumulation of 18FDG.
RESULTS: 18FDG PET detected more lesions than 99mTc MDP scintigraphy (mean,
14.1 and 7.8 lesions, respectively; P < .01). However, 18FDG detected
fewer bone metastases compared with 99mTc MDP scintigraphy in a subgroup of
patients with osteoblastic disease (P < .05). Higher SUVs were observed
for osteolytic 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 for those patients with high SUVs (> 3.6; P=.4). CONCLUSION:
18FDG PET is superior to bone scintigraphy in the detection of osteolytic
breast cancer metastases, which led to a poorer prognosis. In contrast,
osteoblastic metastases show lower metabolic activity and are frequently
undetectable by PET. The biologic explanation for this observation remains
to be elucidated.
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