Abstract
Objective
The aim of this study was to evaluate a 3D tumor segmentation method for fluorodeoxyglucose positron emission tomography (FDG-PET) in the context of noninvasive estimation of tumor metabolic length (L m), as it correlates with surgical pathology and phantom results.
Methods
Thirty-four patients (7 women, 27 men) with esophageal cancer were retrospectively evaluated. All patients underwent FDG-PET-computed tomography (CT) imaging following endoscopic ultrasound (EUS). Seventeen patients had esophagectomy after PET/CT, without prior neoadjuvant therapy. Tumor length was assessed by EUS (L e, n = 31) and histopathology (L p, n = 17). Images were evaluated quantitatively with a 3D threshold-based region-growing program (Medical Image Processing Analysis and Visualization). L m, total metabolic volume (V m), maximum standardized uptake value (SUVmax), and average SUV (SUVa) over the entire tumor were obtained for several threshold values (mean activity in the liver plus 0-, 1-, 2-, 3-, and 4-SD of the activity in the liver).
Results
L m showed a good correlation with L p for all thresholds (best correlation for L m(2-SD), r = 0.74, P < 0.001). A positive nonsignificant correlation was observed between L p and L e (r = 0.30, P = 0.29). L m(2-SD) correlated well with L e (r = 0.71, P < 0.001). Good correlations were also observed between L m(2-SD) and V m(2-SD) (r = 0.89, P < 0.001) and SUVa(2-SD) (r = 0.38, P < 0.05). V m(2-SD) also had a significant correlation with L p (r = 0.61, P < 0.05) and L e (r = 0.57, P < 0.001).
Conclusions
FDG-PET-derived tumor metabolic length of untreated esophageal carcinomas correlates well with surgical pathology results, and provides preliminary evidence that noninvasive delineation of the superior and inferior extent of viable tumor involvement might be feasible using computer-generated metabolic length measurements.
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Mamede, M., Fakhri, G., Abreu-e-Lima, P. et al. Pre-operative estimation of esophageal tumor metabolic length in FDG-PET images with surgical pathology confirmation. Ann Nucl Med 21, 553–562 (2007). https://doi.org/10.1007/s12149-007-0040-0
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DOI: https://doi.org/10.1007/s12149-007-0040-0