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      Feasibility of Radio-Guided Surgery with 68Gallium-DOTATATE in Patients with Gastro-Entero-Pancreatic Neuroendocrine Tumors

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          Abstract

          Background.

          Surgery is the only definitive therapy for gastro-entero-pancreatic neuroendocrine tumors (GEP-NETs), and achieving complete tumor resection is an important prognostic factor. Radiopharmaceuticals such as 68Ga-DOTA peptides have been developed that offer superior accuracy for localization of GEPNETs. The study aim was to determine the feasibility of radio-guided surgery (RGS) using 68Ga-DOTATATE in patients with primary and recurrent GEPNETs.

          Methods.

          Fourteen patients with GEPNETs were enrolled onto a prospective study to determine the feasibility of RGS with 68Ga-DOTATATE. Findings from preoperative imaging, intraoperative exploration, RGS, and pathology were analyzed.

          Results.

          The median decay corrected target count rate was 172.6 (range 28.15–2341) for tumors, with a tumor-to-background ratio (TBR) of 4.46 (range 1.6–43.56). The median lesion size was 1.55 (range 0.5–15) cm. There was no significant correlation between preoperative imaging maximum standardized uptake value (SUV max) of the lesions and TBR (Spearman r = − 0.01, p = 0.9), TBR and tumor size (Spearman r = 0.29, p = 0.14), and SUV max and tumor size (Spearman r = 0.22, p = 0.28). The probe showed correct identification for gastric and small intestine neuroendocrine tumor (NET), including lymph node metastasis in 17 (81.0 %) of 21 cases, with a median TBR of 3.5 (1.6–40.2). For pancreatic NETs and lymph node metastasis, 16 (66.7 %) of 24 were correctly identified by RGS.

          Conclusions.

          Our study shows that RGS with 68Ga-DOTATATE is feasible and correctly confirms bowel NETs and metastatic mesenteric lymph nodes. Further studies are needed to determine the benefit of RGS with 68Ga-DOTATATE.

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          Author and article information

          Journal
          9420840
          8578
          Ann Surg Oncol
          Ann. Surg. Oncol.
          Annals of surgical oncology
          1068-9265
          1534-4681
          8 January 2020
          08 September 2015
          December 2015
          14 January 2020
          : 22
          : Suppl 3
          : S676-S682
          Affiliations
          [1 ]Endocrine Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD;
          [2 ]Positron Emission Tomography Department, Warren Grant Magnusson Clinical Center, National Institutes of Health, Bethesda, MD;
          [3 ]Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, MD
          Author notes
          Article
          PMC6959518 PMC6959518 6959518 nihpa1066235
          10.1245/s10434-015-4857-9
          6959518
          26350374
          55d465ba-0e1c-400f-b653-59d5774bb9d1
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