Clinical diagnosis of skeletal tumors can be difficult, because such lesion
s compose a large, heterogeneous group of entities with different biologic
behaviors. The aim of this prospective study was to assess the value of PET
in grading tumors and tumorlike lesions of bone. Methods: Two hundred two
patients with suspected primary bone tumors were investigated using FDG PET
. Uptake of FDG was evaluated semiquantitatively by determining the tumor-t
o-background ratio (T/B). All patients underwent biopsy, resulting in the h
istologic detection of 70 high-grade sarcomas, 21 low-grade sarcomas, 40 be
nign tumors, 47 tumorlike lesions, 6 osseous lymphomas, 6 plasmacytomas, an
d 12 metastases of an unknown primary tumor. Results: All lesions, with the
exception of 3 benign tumors, were detected by increased FDG uptake. Altho
ugh sarcomas showed significantly higher T/Bs than did latent or active ben
ign lesions (P < 0.001), aggressive benign lesions could not be distinguish
ed from sarcomas. Using a T/B cutoff level for malignancy of 3.0, the sensi
tivity of FDG PET was 93.0%, the specificity was 66.7%, and the accuracy wa
s 81.7%. Conclusion: FDG PET provides a promising tool for estimating the b
iologic activity of skeletal lesions, implicating consequences for the choi
ce of surgical strategy.