Prostate specific membrane antigen (PSMA) PET/CT is an established imaging modality at initial staging and biochemical recurrence. However, cost and limited access have created challenges to its incorporation in the United States Healthcare system and lead to suboptimal utilization of this new modality. In our single institutional demographic study, European Ancestry patients had disproportionate access to PSMA PET/CT despite the commercial availability of the agent. African American patients were once again more likely to be scanned as a clinical trial patient than as a standard of care patient. 18F-DCFPyL PET/CT was offered predominantly by institutions located in wealthy neighborhoods with a predominance of men with European ancestry. If geographic access was omitted, we found that the upfront costs of 18F-DCFPyL PET/CT was greater than alternative prostate cancer-related imaging options. However, we were able to demonstrate that total lifetime costs were reduced when PSMA PET/CT was used due to the radiopharmaceutical’s ability to detect aggressive disease at earlier stages.
To address the stark disparities demonstrated in our study, more centers nationwide need to offer PSMA PET/CT Imaging. Commercially, new PSMA agents and cost competition may also help address disparity-related concerns in the United States Healthcare system, especially when considering the increasing importance of PSMA PET evaluation prior to PSMA-targeted radionuclide therapy.
Written by: Kritika Subramanian, MD,1 Joseph R Osborne, MD, PhD,1 & Jones T Nauseef, MD, PhD
- Division of Molecular Imaging and Therapeutics, Department of Radiology, Weill Cornell Medicine, New York, NY, USA.
- Department of Medical Oncology, Weill Cornell Medicine, New York, NY, USA.
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