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Non-prostate cancer tumours: incidence on 18F-DCFPyL PSMA PET/CT and uptake characteristics in 1445 patients.
Perry, Elisa; Talwar, Arpit; Sharma, Sanjana; O'Connor, Daisy; Wong, Lih-Ming; Taubman, Kim; Sutherland, Tom R.
Affiliation
  • Perry E; Pacific Radiology, Level 1, 123 Victoria Street, Christchurch, Canterbury, New Zealand, 8013. elisa.perry@mh.org.au.
  • Talwar A; St. Vincent's Hospital, Department of Medical Imaging, Melbourne, Victoria, Australia. elisa.perry@mh.org.au.
  • Sharma S; Faculty of Medicine, University of Melbourne, Melbourne, Victoria, Australia. elisa.perry@mh.org.au.
  • O'Connor D; St. Vincent's Hospital, Department of Medical Imaging, Melbourne, Victoria, Australia.
  • Wong LM; St. Vincent's Hospital, Department of Medical Imaging, Melbourne, Victoria, Australia.
  • Taubman K; Pacific Radiology, Level 1, 123 Victoria Street, Christchurch, Canterbury, New Zealand, 8013.
  • Sutherland TR; St. Vincent's Hospital, Department of Urology, Melbourne, Victoria, Australia.
Eur J Nucl Med Mol Imaging ; 49(9): 3277-3288, 2022 07.
Article in En | MEDLINE | ID: mdl-35254481
ABSTRACT

PURPOSE:

With increasing use of PSMA PET/CT in the staging and restaging of prostate cancer (PCa), the identification of non-prostate cancer tumours (NPCaT) has become an increasing clinical dilemma. Atypical presentations of PSMA expression in prostate cancer and expression in NPCaT are not well established. Understanding the normal and abnormal distribution of PSMA expression is essential in preparing clinically relevant reports and in guiding multidisciplinary discussion and decisions.

METHODS:

Retrospective review of 1445 consecutive 18F-DCFPyL PSMA PET/CT studies by experienced radiologists and nuclear medicine physicians. Lesions indeterminate for PCa were identified. Correlation was made with patient records, biopsy results, and dedicated imaging. Lesions were then categorized into four groups 1. Confirmed prostate cancer, metastases, 2. NPCaT 3. Benign, and 4. Indeterminate lesions.

RESULTS:

68/1445 patients had lesions atypical for prostate cancer metastases. These comprised 8/68 (11.8%) atypical prostate cancer metastases, 17/68 (25.0%) NPCaT, 29/68 (42.6%) indeterminate, and 14/68 (20.6%) benign. In the context of the entire cohort, these are adjusted to 8/1445 (0.6%), 17/1445 (1.2%), 29/1445 (2.0%), and 14/1445 (1.0%) respectively. With the exception of Renal Cell Carcinoma (RCC), NPCaT demonstrated no or low PSMA expression. A similar trend was also observed for indeterminate and benign lesions. Conversely, most atypical PCa metastases demonstrated intermediate or high PSMA expression.

CONCLUSION:

18F-DCFPyL PSMA PET/CT detection of NPCaT is low. Lesions demonstrating intermediate to high PSMA expression were exclusively prostate cancer metastases, aside from RCC, and lesions detected in organs with high background expression.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Carcinoma, Renal Cell / Kidney Neoplasms Type of study: Incidence_studies / Prognostic_studies / Risk_factors_studies Limits: Humans / Male Language: En Journal: Eur J Nucl Med Mol Imaging Journal subject: MEDICINA NUCLEAR Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Carcinoma, Renal Cell / Kidney Neoplasms Type of study: Incidence_studies / Prognostic_studies / Risk_factors_studies Limits: Humans / Male Language: En Journal: Eur J Nucl Med Mol Imaging Journal subject: MEDICINA NUCLEAR Year: 2022 Document type: Article