Cc. Meltzer et al., Whole-body FDG positron emission tomographic imaging for staging esophageal cancer - Comparison with computed tomography, CLIN NUCL M, 25(11), 2000, pp. 882-887
Purpose: The aim of the authors in this study was to critically evaluate th
e role of whole-body positron emission tomographic (PET) imaging with fluor
ine-18 fluorodeoxyglucose (FDG) in staging esophageal cancer, and further t
o compare this method with conventional imaging with computed tomography (C
T).
Materials and Methods: The authors performed independent, blinded retrospec
tive evaluations of FDG PET images obtained in 47 patients referred for the
initial staging of esophageal cancer before minimally invasive surgical st
aging. Twenty PET studies from patients with nonesophageal thoracic cancers
were randomly selected for inclusion in the PET readings. In a subset of 3
7 of 47 cases, the PET findings were compared with independent readings of
CT studies acquired within the same 6-week interval, The utility of the ima
ging findings was evaluated using a high-sensitivity interpretation (i.e.,
assigning equivocal findings as positive) and a low-sensitivity interpretat
ion (i.e., assigning equivocal findings as negative).
Results: PET was less sensitive (41% in high-sensitivity mode, 35% in low-s
ensitivity mode) than CT (63% to 87%) for diagnosing tumor involvement in l
ocoregional lymph nodes, which was identified by surgical assessment in 72%
of patients. Notable, however, was the greater specificity of PET-determin
ed nodal sites (10 approximately 90%) compared with CT (14% to 43%). In det
ecting histologically proved distant metastases (n = 10), PET performed con
siderably better when applied in the high-sensitivity mode, with a sensitiv
ity rate of approximately 70% and a specificity rate of more than 90% in th
e total group and in the subset of patients with correlative CT data, In th
e low-sensitivity mode, CT identified only two of seven metastatic sites, w
hereas the high-sensitivity mode resulted in an unacceptably high rate of f
alse-positive readings (positive predictive value, 29%). PET correctly iden
tified one additional site of metastasis that was not detected by CT.
Conclusions: The relatively low sensitivity of PET for identifying locoregi
onal lesions precludes its replacement of conventional CT staging. However,
the primary advantage of PET imaging is its superior specificity for tumor
detection and improved diagnostic value for distant metastatic sites, feat
ures that may substantially affect patient management decisions. In conclus
ion, PET imaging is useful in the initial staging of esophageal cancer and
provides additional and complementary information to that obtained by CT im
aging.