Publication

Recurrent prostate cancer detection with anti-3-[F-18]FACBC PET/CT: comparison with CT

Downloadable Content

Persistent URL
Last modified
  • 03/03/2025
Type of Material
Authors
    Oluwaseun A. Odewole, Emory UniversityFunmilayo Tade, Emory UniversityPeter Nieh, Emory UniversityBital Savir-Baruch, Loyola UnivAshesh Jani, Emory UniversityViraj Master, Emory UniversityPeter Rossi, Emory UniversityRaghuveer Halkar, Emory UniversityAdeboye Osunkoya, Emory UniversityOladunni Akin-Akintayo, Emory UniversityChao Zhang, Emory UniversityZhengjia Chen, Emory UniversityMark Goodman, Emory UniversityDavid Schuster, Emory University
Language
  • English
Date
  • 2016-09-01
Publisher
  • Springer Verlag
Publication Version
Copyright Statement
  • © 2016, Springer-Verlag Berlin Heidelberg.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1619-7070
Volume
  • 43
Issue
  • 10
Start Page
  • 1773
End Page
  • 1783
Grant/Funding Information
  • David Schuster, Oluwaseun Odewole, Funmilayo Tade, Oladunni Akin-Akintayo. Although not impacting this study, funding is or has been received from Blue Earth Diagnostics Ltd. and Nihon Medi-Physics Co., Ltd. through the Emory University Office of Sponsored Projects for other clinical trials using FACBC (fluciclovine).
  • National Institutes of Health Grant (R01CA129356) and Georgia Cancer Coalition.
Abstract
  • Purpose: To compare the diagnostic performance of the synthetic amino acid analogue PET radiotracer anti-3-[ 18 F]FACBC (fluciclovine) with that of CT in the detection of recurrent prostate carcinoma. Methods: This was a retrospective analysis of 53 bone scan-negative patients with suspected recurrent prostate carcinoma who underwent fluciclovine PET/CT and routine clinical CT within 90 days of each other. The correlation between imaging findings and histology and clinical follow-up was evaluated. Positivity rates and diagnostic performance were calculated for fluciclovine PET/CT and CT. Results: Of 53 fluciclovine PET/CT and 53 CT examinations, 41 (77.4 %) and 10 (18.9 %), respectively, had positive findings for recurrent disease. Positivity rates were higher with fluciclovine PET/CT than with CT at all prostate-specific antigen (PSA) levels, PSA doubling times and original Gleason scores. In the prostate/bed, fluciclovine PET/CT was true-positive in 31 and CT was true-positive in 4 of 51 patients who met the reference standard. In extraprostatic regions, fluciclovine PET/CT was true-positive in 12 and CT was true-positive in 3 of 41 patients who met the reference standard. Of the 43 index lesions used to prove positivity, 42 (97.7 %) had histological proof. In 51 patients with sufficient follow-up to calculate diagnostic performance in the prostate/bed, fluciclovine PET/CT demonstrated a sensitivity of 88.6 %, a specificity of 56.3 %, an accuracy of 78.4 %, a positive predictive value (PPV) of 81.6 %, and a negative predictive value (NPV) of 69.2 %; the respective values for CT were 11.4 %, 87.5 %, 35.3 %, 66.7 % and 31.1 %. In 41 patients with sufficient follow-up to calculate diagnostic performance in extraprostatic regions, fluciclovine PET/CT demonstrated a sensitivity of 46.2 %, a specificity of 100 %, an accuracy of 65.9 %, a PPV of 100 %, and an NPV of 51.7 %; the respective values for CT were 11.5 %, 100 %, 43.9 %, 100 % and 39.5 %. Conclusion: The diagnostic performance of fluciclovine PET/CT in recurrent prostate cancer is superior to that of CT and fluciclovine PET/CT provides better delineation of prostatic from extraprostatic recurrence.
Author Notes
  • Corresponding Author: 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, Radiology
  • Health Sciences, Medicine and Surgery

Tools

Relations

In Collection:

Items