4.6 Article

A Prospective Pilot Study of 89Zr-J591/Prostate Specific Membrane Antigen Positron Emission Tomography in Men with Localized Prostate Cancer Undergoing Radical Prostatectomy

Journal

JOURNAL OF UROLOGY
Volume 191, Issue 5, Pages 1439-1445

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.juro.2013.10.041

Keywords

prostatic neoplasms; positron-emission tomography; glutamate carboxypeptidase II, human; zirconium; J591 monoclonal antibody

Funding

  1. Center to Reduce Cancer Health Disparity Grant [R21 CA153177-03]
  2. Starr Consortium
  3. Ludwig Center for Targeted Radioimmunotherapy and Diagnosis
  4. Geoffrey Beane Cancer Consortia
  5. Radiochemistry and Molecular Imaging Probe Core
  6. David H. Koch Foundation
  7. Robert Dow Foundation
  8. Frederick J. and Theresa Dow Wallace Fund of New York Community Trust
  9. Clinical Translational Science Center Grant [UL1-TR000457-06]
  10. James P. McCarron Foundation

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Purpose: In this pilot study we explored the feasibility of Zr-89 labeled J591 monoclonal antibody positron emission tomography of localized prostate cancer. Materials and Methods: Before scheduled radical prostatectomy 11 patients were injected intravenously with Zr-89-J591, followed 6 days later by whole body positron emission tomography. Patients underwent surgery the day after imaging. Specimens were imaged by ex vivo micro positron emission tomography and a custom 3 Tesla magnetic resonance scanner coil. Positron emission tomography images and histopathology were correlated. Results: Median patient age was 61 years (range 47 to 68), median prostate specific antigen was 5.2 ng/ml (range 3.5 to 12.0) and median biopsy Gleason score of the 11 index lesions was 7 (range 7 to 9). On histopathology 22 lesions were identified. Median lesion size was 5.5 mm (range 2 to 21) and median Gleason score after radical prostatectomy was 7 (range 6 to 9). Eight of 11 index lesions (72.7%) were identified by in vivo positron emission tomography. Lesion identification improved with increasing lesion size for in vivo and ex vivo positron emission tomography (each p<0.0001), and increasing Gleason score (p=0.14 and 0.01, respectively). Standardized uptake values appeared to correlate with increased Gleason score but not significantly (p=0.19). Conclusions: To our knowledge this is the first report of Zr-89-J591/prostate specific membrane antigen positron emission tomography in localized prostate cancer cases. In this setting Zr-89-J591 bound to tumor foci in situ and positron emission tomography identified primarily Gleason score 7 or greater and larger tumors, likely corresponding to clinically significant disease warranting definitive therapy. A future, larger clinical validation trial is planned to better define the usefulness of Zr-89-J591 positron emission tomography for localized prostate cancer.

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