Publication

Prospective evaluation of fluciclovine (F-18) PET-CT and MRI in detection of recurrent prostate cancer in non-prostatectomy patients

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Last modified
  • 05/15/2025
Type of Material
Authors
    Oladunni Akin-Akintayo, Emory UniversityFunmilayo Tade, Emory UniversityPardeep Mittal, Emory UniversityCarlos Moreno, Emory UniversityPeter T Nieh, Emory UniversityPeter J Rossi, Emory UniversityDattatraya Patil, Emory UniversityRaghuveer Halkar, Emory UniversityBaowei Fei, Emory UniversityViraj Master, Emory UniversityAshesh Jani, Emory UniversityHiroumi Kitajima, Emory UniversityAdeboye O. Osunkoya, Emory UniversityClaudia Ormenisan-Gherasim, Emory UniversityMark Goodman, Emory UniversityDavid M Schuster, Emory University
Language
  • English
Date
  • 2018-05-01
Publisher
  • Elsevier: 12 months
Publication Version
Copyright Statement
  • © 2018 Elsevier B.V.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0720-048X
Volume
  • 102
Start Page
  • 1
End Page
  • 8
Grant/Funding Information
  • This study was funded by National Institutes of Health (NIH P50 CA12830, R21CA176684, R01CA156775 and R01CA204254).
  • Blue Earth Diagnostics Ltd. provided fluciclovine synthesis cassettes to Emory University for this project.
Abstract
  • Purpose: To investigate the disease detection rate, diagnostic performance and interobserver agreement of fluciclovine ( 18 F) PET-CT and multiparametric magnetic resonance imaging (mpMR) in recurrent prostate cancer. Methods: Twenty-four patients with biochemical failure after non-prostatectomy definitive therapy, 16/24 of whom had undergone brachytherapy, underwent fluciclovine PET-CT and mpMR with interpretation by expert readers blinded to patient history, PSA and other imaging results. Reference standard was established via a multidisciplinary truth panel utilizing histology and clinical follow-up (22.9 ± 10.5 months) and emphasizing biochemical control. The truth panel was blinded to investigative imaging results. Diagnostic performance and interobserver agreement (kappa) for the prostate and extraprostatic regions were calculated for each of 2 readers for PET-CT (P1 and P2) and 2 different readers for mpMR (M1 and M2). Results: On a whole body basis, the detection rate for fluciclovine PET-CT was 94.7% (both readers), while it ranged from 31.6–36.8% for mpMR. Kappa for fluciclovine PET-CT was 0.90 in the prostate and 1.0 in the extraprostatic regions. For mpMR, kappa was 0.25 and 0.74, respectively. In the prostate, 22/24 patients met the reference standard with 13 malignant and 9 benign results. Sensitivity, specificity and positive predictive value (PPV) were 100.0%, 11.1% and 61.9%, respectively for both PET readers. For mpMR readers, values ranged from 15.4–38.5% for sensitivity, 55.6–77.8% for specificity and 50.0–55.6% for PPV. For extraprostatic disease determination, 18/24 patients met the reference standard. Sensitivity, specificity and PPV were 87.5%, 90.0% and 87.5%, respectively, for fluciclovine PET-CT, while for mpMR, sensitivity ranged from 50 to 75%, specificity 70–80% and PPV 57–75%. Conclusion: The disease detection rate for fluciclovine PET-CT in non-prostatectomy patients with biochemical failure was 94.7% versus 31.6–36.8% for mpMR. For extraprostatic disease detection, fluciclovine PET-CT had overall better diagnostic performance than mpMR. For the treated prostate, fluciclovine PET-CT had high sensitivity though low specificity for disease detection, while mpMR had higher specificity, though low sensitivity. Interobserver agreement was also higher with fluciclovine PET-CT compared with mpMR.
Author Notes
  • David M. Schuster, MD; Division of Nuclear Medicine and Molecular Imaging, Department of Radiology and Imaging Sciences, Emory University Hospital, 1364 Clifton Road, Atlanta, GA 30322. Telephone: 404-712-4859, Fax: 404-712-4860, dschust@emory.edu.
Keywords
Research Categories
  • Health Sciences, Pathology
  • Health Sciences, Radiology
  • Health Sciences, Oncology

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