Abstract

We investigated the diagnostic performance of Somatostatin Receptor Positron Emission Tomography/Computed Tomography (SSR-PET/CT) for the detection of primary lesion and initial staging of pancreatic neuroendocrine tumors (pNETs). A comprehensive literature search up to January 2020 was performed selecting studies in presence of: sample size ≥10 patients; index test (i.e., 68Ga-DOTATOC or 68Ga-DOTANOC or 68Ga-DOTATATE PET/CT); and outcomes (i.e., detection rate (DR), true positive, true negative, false positive, and false-negative). The methodological quality was evaluated with QUADAS-2. Pooled DR and pooled sensitivity and specificity for the identification of the primary tumor were assessed by a patient-based and a lesion-based analysis. Thirty-eight studies were selected for the qualitative analysis, while 18 papers were included in the meta-analysis. The number of pNET patients ranged from 10 to 142, for a total of 1143 subjects. At patient-based analysis, the pooled sensitivity and specificity for the assessment of primary pNET were 79.6% (95% confidence interval (95%CI): 71–87%) and 95% (95%CI: 75–100%) with a heterogeneity of 59.6% and 51.5%, respectively. Pooled DR for the primary lesion was 81% (95%CI: 65–90%) and 92% (95%CI: 80–97%), respectively, at patient-based and lesion-based analysis. In conclusion, SSR-PET/CT has high DR and diagnostic performances for primary lesion and initial staging of pNETs.

Highlights

  • The incidence of pancreatic neuroendocrine tumors is less or equal to one case per one hundred thousand people per-year, and they account for roughly 5% of all pancreatic cancers.in the last few decades, their incidence has risen [1,2].Many biological features make these tumors clinically heterogeneous, including mutational status [3,4], hormone production, and histopathological grade

  • In the present systematic review and meta-analysis, we investigate the diagnostic performance of SSR-positron emission tomography and computed tomography (PET/CT) for the detection of the primary lesion and initial staging of pancreatic neuroendocrine tumors (pNETs)

  • To the best of our knowledge, this is the first systematic review and meta-analysis addressing the identification of the primary lesion and initial staging by using SSR-PET/CT in patients with pNETs

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Summary

Introduction

The incidence of pancreatic neuroendocrine tumors (pNETs) is less or equal to one case per one hundred thousand people per-year, and they account for roughly 5% of all pancreatic cancers.in the last few decades, their incidence has risen [1,2].Many biological features make these tumors clinically heterogeneous, including mutational status [3,4], hormone production, and histopathological grade. The incidence of pancreatic neuroendocrine tumors (pNETs) is less or equal to one case per one hundred thousand people per-year, and they account for roughly 5% of all pancreatic cancers. In well-differentiated pNETs (G1, G2, and well-differentiated G3) the slow cancer growth is related to good long-term survival even in the presence of liver metastases [5], while poorly differentiated G3 neuroendocrine carcinomas (NECs) show higher proliferation rates and lower overall survival [6]. Tumor grade is strictly related to the expression of somatostatin receptors (SSR1-5) on the neoplastic cellular surface [6,7]. In low-grade pNETs, the high SSR expression allows the therapeutic use of somatostatin analogs and makes these neoplasms ideal for targeted radionuclide imaging [8]. The down-regulation of SSR makes high-grade NEC less suitable for these approaches

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