Background: Gallium-DOTATATE positron emission tomography-computed tomography (PET CT) has shown superior accuracy in detecting grade 1 and 2 neuroendocrine tumors over previous imaging modalities and was recently included in National Comprehensive Cancer Network guidelines. It remains unclear which patients benefit most from this imaging modality. We therefore reviewed our initial experience with Gallium-DOTATATE PET CT to evaluate its usefulness in diagnosing, staging, and surveilling neuroendocrine tumors.
Methods: Records of patients who underwent Gallium-DOTATATE PET CT from March to December 2017 were prospectively evaluated. The primary endpoint was whether Gallium-DOTATATE PET CT changes treatment in patients with neuroendocrine tumors. Descriptive statistics, Fisher exact tests, and nested logistic regressions were conducted.
Results: A total of 50 consecutive patients were included. Of these, 41 patients (82%) had a biopsy-proven neuroendocrine tumor at the time of imaging. The remaining 9 patients (18%) had symptoms or biochemistry suggestive of a neuroendocrine tumor with negative cross-sectional imaging. Gallium-DOTATATE PET CT changed management in 33 patients (66%). There were 24 patients with intermodality changes in management and 9 patients with intramodality changes in management. Patients with scans performed for staging had a higher likelihood of a change in management (P = .006).
Conclusion: Performing Gallium-DOTATATE PET CT should be considered for staging and surveillance of neuroendocrine tumors because it is frequently associated with changes in management.
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http://dx.doi.org/10.1016/j.surg.2018.03.030 | DOI Listing |
Endocrinol Diabetes Metab Case Rep
July 2024
Alice Springs Hospital, Alice Springs, Northern Territory, Australia.
Radiol Case Rep
October 2024
Department of Radiology, The Royal Free Hospital, NHS Foundation Trust, London, United Kingdom.
BMJ Case Rep
December 2023
Department of Radiotherapy, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
A man in his early 20s presented to us in the outpatient department with a history of diarrhoea for 4 months. Investigations revealed elevated serum chromogranin levels and an intensely avid lesion in the gastrohepatic ligament in Gallium DOTATATE positron emission tomography (PET). The tumour was excised laparoscopically, and no other lesions were seen.
View Article and Find Full Text PDFAACE Clin Case Rep
May 2023
Department of Endocrinology, Sultan Qaboos Comprehensive Cancer Care and Research Centre (SQCCCRC), Muscat, Sultanate of Oman.
Background/objective: To report a dramatic and immediate clinical and biochemical response during treatment with octreotide in a patient with a functioning mesenteric paraganglioma (PGL).
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J Clin Med
February 2023
Department of Medicine, Boston University School of Medicine and Boston Medical Center, Boston, MA 02118, USA.
Pancreatic neuroendocrine tumors, or pNETs, represent a rare and clinically heterogenous subset of pancreatic neoplasms. One such pNET, the insulinoma, is found to be malignant in just 4% of all insulinomas. Due to the exceedingly uncommon occurrence of these tumors, there is controversy regarding the optimal evidence-based management for these patients.
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