Ann Surg Treat Res.  2020 Apr;98(4):184-189. 10.4174/astr.2020.98.4.184.

The efficacy of 18F-FDG PET/CT in the preoperative evaluation of pancreatic lesions

Affiliations
  • 1Department of General Surgery, Faculty of Medicine, Cukurova University, Adana, Turkey
  • 2Department of Surgical Oncology, Faculty of Medicine, Cukurova University, Adana, Turkey
  • 3Department of Nuclear Medicine, Faculty of Medicine, Cukurova University, Adana, Turkey

Abstract

Purpose
Since the treatment strategy for benign and malignant pancreatic lesions differ, we aimed to evaluate the clinical value of PET/CT in the diagnosis and management of pancreatic lesions.
Methods
Ninety patients who had a histologically confirmed pancreatic lesion were studied. Receiver operating characteristic (ROC) curve analysis was used to investigate the ability of PET/CT to differentiate malignant lesions from benign tumors.
Results
The malignant and benign groups comprised 64 and 26 patients, respectively. Despite the similarity in the size of primary tumors (P = 0.588), the mean maximum standardized uptake values (SUVmax) obtained from PET/CT imaging were significantly higher in malignant lesions (9.36 ± 5.9) than those of benign tumors (1.04 ± 2.6, P < 0.001). ROC analysis showed that the optimal SUVmax cutoff value for differentiating malignant lesions (to an accuracy of 91%; 95% confidence interval, 83%–98%) from benign tumors was 3.9 (sensitivity, 92.2%; specificity, 84.6%).
Conclusion
PET/CT evaluation of pancreatic lesions confers advantages including fine assessment of malignant potential with high sensitivity and accuracy using a threshold SUVmax value of 3.9.

Keyword

Chronic pancreatitis; Pancreas; Pancreatic neoplasms; Pancreatic pseudocyst; Positron emission tomography computed tomography

Figure

  • Fig. 1 PET/CT images of chronic pancreatitis patients with increased maximum standardized uptake values (SUVmax). (A) SUVmax: 7.95. (B) SUVmax: 9.3.

  • Fig. 2 Receiver operating characteristic (ROC) curve for differentiating benign and malignant pancreatic lesions.


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