Prospective evaluation of PSMA-targeted 18F-DCFPYL PET/CT in men with biochemical failure after radical prostatectomy for prostate cancer

Steven P. Rowe*, Scott P. Campbell, Margarita Mana-Ay, Zsolt Szabo, Mohamad E. Allaf, Kenneth J. Pienta, Martin G. Pomper, Ashley E. Ross, Michael A. Gorin

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

58 Scopus citations

Abstract

Our purpose is to provide the results of a prospective study evaluating prostate-specific membrane antigen–targeted 18F-DCFPyL (2-(3-{1-carboxy-5-[(6-18F-fluoro-pyridine-3-carbonyl)-amino]-pentyl}-ureido)pentanedioic acid) PET/CT in patients with biochemical failure after radical prostatectomy for prostate cancer (PCa). Methods: Thirty-one patients with postprostatectomy serum prostate-specific antigen (PSA) levels of at least 0.2 ng/mL and negative conventional imaging results were enrolled in this study and imaged with 18F-DCFPyL PET/CT. A consensus central review identified foci of radiotracer uptake consistent with sites of PCa. Descriptive statistics were used. Results: Twenty-one patients (67.7%) had at least 1 finding on 18F-DCFPyL PET/CT consistent with a site of PCa. Imaging was positive in 59.1% of patients with a PSA level of less than 1.0 ng/mL and in 88.9% of patients with a PSA level of more than 1.0 ng/mL. The median SUVmax across all lesions was 11.6 (range, 1.5–57.6). Conclusion: In this prospective study using the prostate-specific membrane antigen–targeted PET agent 18F-DCFPyL, most patients with biochemical failure after radical prostatectomy had foci of suggestive uptake, even at low serum PSA levels.

Original languageEnglish (US)
Pages (from-to)58-61
Number of pages4
JournalJournal of Nuclear Medicine
Volume61
Issue number1
DOIs
StatePublished - Jan 2020

Funding

This work was funded by Progenics Pharmaceuticals, Inc.; the Prostate Cancer Foundation; National Institutes of Health grants CA134675, CA183031, CA184228, and EB024495; and philanthropy raised by the James Buchanan Brady Urological Institute and Department of Urology. Martin G. Pomper is a coinventor on a patent covering 18F-DCFPyL and is entitled to a portion of any licensing fees and royalties generated by this technology. This arrangement has been reviewed and approved by the Johns Hopkins University in accordance with its conflict-of-interest policies. He has also received research funding from Progenics Pharmaceuticals, the licensee of 18F-DCFPyL. Michael A. Gorin has served as a consultant to, and has received research funding from, Progenics Pharmaceuticals. Kenneth J. Pienta and Steven P. Rowe have also received research funding from Progenics Pharmaceuticals. No other potential conflict of interest relevant to this article was reported.

Keywords

  • Biochemical persistence
  • Biochemical recurrence
  • Genitourinary
  • Oncology
  • PET/CT
  • Prostate-specific membrane antigen

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging

Fingerprint

Dive into the research topics of 'Prospective evaluation of PSMA-targeted 18F-DCFPYL PET/CT in men with biochemical failure after radical prostatectomy for prostate cancer'. Together they form a unique fingerprint.

Cite this