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18F-DCFPyL PET/CT Imaging in Patients with Biochemical Recurrence Prostate Cancer after Primary Local Therapy

  1. Author:
    Mena, Esther
    Lindenberg, Maria Liza
    Turkbey, Ismael Baris
    Shih, Joanna H
    Harmon,Stephanie
    Lim, Ilhan
    Lin, Frank I
    Adler,Stephen
    Eclarinal, Philip
    McKinney, Yolanda
    Citrin, Deborah
    Dahut, William
    Wood, Bradford
    Krishnasamy, Venkatesh
    Chang, Richard
    Levy, Elliot
    Merino, Maria
    Pinto, Peter
    Eary, Janet F
    Choyke, Peter L
  2. Author Address

    Molecular Imaging Program. National Cancer Institute. NIH, United States., Division of Cancer Treatment and Diagnosis: Biometric Research Program. National Cancer Institute. NIH., Research Clinical Research Directorate, Frederick National Laboratory for Cancer Research Sponsored by National Cancer Institute. NIH., Radiation Oncology Branch, CCR. NCI, NIH., Genitourinary Malignancies, NCI, NIH., Center of Interventional Oncology. NCI, NIH., Laboratory of Pathology, NCI, NIH., Urologic Oncology, NCI, NIH., Cancer Imaging Program, NCI, NIH.,
    1. Year: 2020
    2. Date: JUN 1
    3. Epub Date: 2019 11 01
  1. Journal: Journal of nuclear medicine : official publication, Society of Nuclear Medicine
    1. 61
    2. 6
    3. Pages: 881-889
  2. Type of Article: Article
  3. ISSN: 0161-5505
  1. Abstract:

    Objective: To investigate the lesion detection rate of 18F-DCFPyL-PET/CT, a prostate-specific membrane antigen (PSMA) targeted PET agent, in biochemical relapse prostate cancer patients after primary local therapy. Methods: This is a prospective institutional review board-approved study of 90 patients with documented biochemical recurrence (median PSA 2.5 ng/mL, range 0.21-35.5 ng/mL) with negative conventional imaging after primary local therapies, including radical prostatectomy (n = 38), radiation (n = 27) or combination (n = 25). Patients on androgen deprivation therapy were excluded. Patients underwent whole-body 18F-DCFPyL-PET/CT (299.9±15.5 MBq) at 2 h p.i. PSMA-PET lesion detection rate was correlated with PSA, PSA kinetics and original primary tumor grade. Results: Seventy patients (77.8%) showed a positive PSMA-PET scan, identifying a total of 287 lesions: 37 prostate bed foci, 208 lymph nodes, and 42 bone/organ distant sites; 11 patients had a negative scan and 9 patients showed indeterminate lesions, which were considered negative in this study. The detection rates were 47.6% (n = 10/21), 50% (n = 5/10), 88.9% (n = 8/9), and 94% (n = 47/50) for PSA >0.2 to < 0.5, 0.5 to < 1.0, 1 to < 2.0, and =2.0 ng/mL, respectively. In post-surgical patients, PSA, PSAdt and PSAvel correlated with PET results but the same was not true for post-radiation patients. These parameters also correlated with the extent of disease on PET (intrapelvic vs. extrapelvic). There was no significant difference between the rate of positive scans in patients with higher grade vs lower grade primary tumors (Gleason score =4+3 vs < 3+4). Tumor recurrence was histology confirmed in 40% (28/70) of patients. On a per-patient basis, positive predictive value was 93.3% (95% CI, 77.6-99.2%) by histopathologic validation, and 96.2% (95% CI, 86.3-99.7%) by the combination of histology and imaging/clinical follow-up. Conclusion:18F-DCFPyL-PET/CT imaging offers high detection rates in biochemically recurrent prostate cancer patients; and is positive in about 50% of patients with PSA < 0.5 ng/mL, which could substantially impact clinical management. In post-surgical patients, 18F-DCFPyL-PET/CT correlates with PSA, PSAdt and PSAvel suggesting it may have prognostic value. 18F-DCFPyL-PET/CT is highly promising for localizing sites of recurrent prostate cancer. Copyright © 2019 by the Society of Nuclear Medicine and Molecular Imaging, Inc.

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External Sources

  1. DOI: 10.2967/jnumed.119.234799
  2. PMID: 31676732
  3. WOS: 000539159900028
  4. PII : jnumed.119.234799

Library Notes

  1. Fiscal Year: FY2019-2020
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