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A Phase 2/3 Prospective Multicenter Study of the Diagnostic Accuracy of Prostate Specific Membrane Antigen PET/CT with 18F-DCFPyL in Prostate Cancer Patients (OSPREY).
Pienta, Kenneth J; Gorin, Michael A; Rowe, Steven P; Carroll, Peter R; Pouliot, Frédéric; Probst, Stephan; Saperstein, Lawrence; Preston, Mark A; Alva, Ajjai S; Patnaik, Akash; Durack, Jeremy C; Stambler, Nancy; Lin, Tess; Jensen, Jessica; Wong, Vivien; Siegel, Barry A; Morris, Michael J.
Affiliation
  • Pienta KJ; The James Buchanan Brady Urological Institute and Department of Urology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Gorin MA; The James Buchanan Brady Urological Institute and Department of Urology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Rowe SP; The Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Carroll PR; The Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Pouliot F; University of California San Francisco, San Francisco, California.
  • Probst S; CHU de Quebec and Laval University, Quebec City, Quebec.
  • Saperstein L; Jewish General Hospital, Montreal, Quebec.
  • Preston MA; Yale School of Medicine, New Haven, Connecticut.
  • Alva AS; Brigham and Women's Hospital/Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Patnaik A; University of Michigan, Ann Arbor, Michigan.
  • Durack JC; Section of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois.
  • Stambler N; Memorial Sloan Kettering Cancer Center, New York, New York.
  • Lin T; Progenics Pharmaceuticals, Inc., New York, New York.
  • Jensen J; Progenics Pharmaceuticals, Inc., New York, New York.
  • Wong V; Progenics Pharmaceuticals, Inc., New York, New York.
  • Siegel BA; Progenics Pharmaceuticals, Inc., New York, New York.
  • Morris MJ; Mallinckrodt Institute of Radiology and Alvin J. Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri.
J Urol ; 206(1): 52-61, 2021 07.
Article in En | MEDLINE | ID: mdl-33634707
ABSTRACT

PURPOSE:

Prostate specific membrane antigen-targeted positron emission tomography/computerized tomography has the potential to improve the detection and localization of prostate cancer. OSPREY was a prospective trial designed to determine the diagnostic performance of 18F-DCFPyL-positron emission tomography/computerized tomography for detecting sites of metastatic prostate cancer. MATERIALS AND

METHODS:

Two patient populations underwent 18F-DCFPyL-positron emission tomography/computerized tomography. Cohort A enrolled men with high-risk prostate cancer undergoing radical prostatectomy with pelvic lymphadenectomy. Cohort B enrolled patients with suspected recurrent/metastatic prostate cancer on conventional imaging. Three blinded central readers evaluated the 18F-DCFPyL-positron emission tomography/computerized tomography. Diagnostic performance of 18F-DCFPyL-positron emission tomography/computerized tomography was based on imaging results compared to histopathology. In cohort A, detection of pelvic nodal disease (with specificity and sensitivity as co-primary end points) and of extrapelvic metastases were evaluated. In cohort B, sensitivity and positive predictive value for prostate cancer within biopsied lesions were evaluated.

RESULTS:

A total of 385 patients were enrolled. In cohort A (252 evaluable patients), 18F-DCFPyL-positron emission tomography/computerized tomography had median specificity of 97.9% (95% CI 94.5%-99.4%) and median sensitivity of 40.3% (28.1%-52.5%, not meeting prespecified end point) among 3 readers for pelvic nodal involvement; median positive predictive value and negative predictive value were 86.7% (69.7%-95.3%) and 83.2% (78.2%-88.1%), respectively. In cohort B (93 evaluable patients, median prostate specific antigen 11.3 ng/ml), median sensitivity and positive predictive value for extraprostatic lesions were 95.8% (87.8%-99.0%) and 81.9% (73.7%-90.2%), respectively.

CONCLUSIONS:

The primary end point for specificity was met while the primary end point for sensitivity was not. The high positive predictive value observed in both cohorts indicates that 18F-DCFPyL-positive lesions are likely to represent disease, supporting the potential utility of 18F-DCFPyL-positron emission tomography/computerized tomography to stage men with high-risk prostate cancer for nodal or distant metastases, and reliably detect sites of disease in men with suspected metastatic prostate cancer.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Urea / Prostate-Specific Antigen / Positron Emission Tomography Computed Tomography / Lysine Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Aged80 / Humans / Male / Middle aged Language: En Journal: J Urol Year: 2021 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Urea / Prostate-Specific Antigen / Positron Emission Tomography Computed Tomography / Lysine Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Aged80 / Humans / Male / Middle aged Language: En Journal: J Urol Year: 2021 Type: Article