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Asian Journal of Current Research in Clinical Cancer

2023 Volume 3 Issue 2

Enhanced Clinical Decision-Making in Early Prostate Cancer Recurrence Using [18F]Fluciclovine PET/CT


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  1. Department of Oncology, College of Medicine, University of Ibadan, Ibadan, Nigeria.
Abstract

The present study assessed the role of [18F]Fluciclovine PET/CT in detecting early recurrent prostate cancer (PCa) and its influence on treatment decisions. We retrospectively reviewed 58 [18F]Fluciclovine PET/CT scans performed for suspected early recurrence. Detection rates (DR) and semiquantitative parameters were analyzed in relation to biochemical and clinical–pathological characteristics. Clinical follow-up served as the reference standard to determine sensitivity, specificity, accuracy, and predictive values (PPV and NPV). The overall DR was 66%, with lesion-specific rates of 53% in the prostate/prostate bed, 28% in lymph nodes, and 7% in bone. Higher PSA levels were associated with increased detection (p = 0.009), and a PSA threshold of 0.45 ng/mL was identified as optimal. Semiquantitative indices, including SUVmax and SUVmean, were useful in differentiating malignant from benign lesions. The imaging modality achieved a sensitivity of 87.1%, specificity of 80.0%, PPV of 87.1%, NPV of 80.0%, and an overall accuracy of 84.3%. Based on PET/CT findings, therapeutic management was altered in 51% of cases. These results highlight [18F]Fluciclovine PET/CT as a reliable approach for early restaging of PCa, particularly for local recurrence, and suggest that semiquantitative analysis may further improve diagnostic specificity.


How to cite this article
Vancouver
Okoro C, Adebayo F, Bello A. Enhanced Clinical Decision-Making in Early Prostate Cancer Recurrence Using [18F]Fluciclovine PET/CT. Asian J Curr Res Clin Cancer. 2023;3(2):36-50. https://doi.org/10.51847/Nuh7wPRHUj
APA
Okoro, C., Adebayo, F., & Bello, A. (2023). Enhanced Clinical Decision-Making in Early Prostate Cancer Recurrence Using [18F]Fluciclovine PET/CT. Asian Journal of Current Research in Clinical Cancer, 3(2), 36-50. https://doi.org/10.51847/Nuh7wPRHUj

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