4.6 Article

Whole-Body 68Ga-DOTANOC PET/MRI Versus 68Ga-DOTANOC PET/CT in Patients With Neuroendocrine Tumors: A Prospective Study in 28 Patients

期刊

CLINICAL NUCLEAR MEDICINE
卷 42, 期 9, 页码 669-674

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/RLU.0000000000001753

关键词

Ga-68-DOTA peptides; computed tomography; magnetic resonance imaging; neuroendocrine tumors; positron emission tomography

资金

  1. Austrian Science Fund (FWF) [KLIF 382]

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Purpose The aim of this study was to assess the diagnostic performance of simultaneous whole-body Ga-68-DOTANOC PET/MRI compared with Ga-68-DOTANOC PET/CT for detection of distant metastatic disease in patients with well-differentiated neuroendocrine tumors (NETs). Methods Patients with histologically proven, well-differentiated NET (G1 or G2) were included in this prospective, institutional review board-approved study. Patients underwent Ga-68-DOTANOC PET/CT and subsequent Ga-68-DOTANOC PET/MRI after a single tracer injection on the same day for staging or restaging purposes. Images were evaluated for the presence of NET lesions by 2 rater teams, each consisting of a nuclear medicine physician and a radiologist, in an observer-blinded fashion. Overall agreement, accuracy, sensitivity, and specificity, relative to a composite reference standard (consensus review including follow-up data), were calculated. Results Between July 2014 and June 2016, 28 patients were enrolled. Overall agreement and accuracy between the 2 rater teams were 91.7% (95% confidence interval [CI], 87.5%-95.9%) and 97% (95% CI, 94.4%-99.6%) for PET/MRI and 92.3% (95% CI, 88.3%-96.3%) and 94.6% (95% CI, 91.2%-98.1%) for PET/CT, respectively (P = 1.00). Overall, PET/MRI reached 89.8% sensitivity (95% CI, 77.8%-96.6%) and 100% specificity (95% CI, 97%-100%); PET/CT showed 81.6% sensitivity (95% CI, 68%-91.2%) and 100% specificity (95% CI, 97%-100%) for the detection of metastatic disease in NETs. Conclusions Whole-body Ga-68-DOTANOC PET/MRI appears to be comparable to Ga-68-DOTANOC PET/CT for lesion detection in patients with well-differentiated NETs.

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