Beyond the tumor: Recurrence-prone radiomics for prognostication in negative PSMA PET/CT scans of prostate cancer.
Authors
Affiliations (15)
Affiliations (15)
- BC Cancer Research Centre, Vancouver, Vancouver, British Columbia, V5Z 1L3, Canada.
- Department of Medical Imaging, University of Toronto, Toronto, Toronto, Ontario, M5S 1A1, Canada.
- Institut de Biologie Valrose , Inserm, Nice, France, nice, 06108, France.
- BC Cancer Agency, 675 10th Ave W, Vancouver, Vancouver, British Columbia, V5Z 1G1, Canada.
- Department of Radiation Medicine and Applied Sciences, University of California San Diego, Moores Cancer Center, 3855 Health Sciences Drive, La Jolla, California, 92093-0865, United States.
- BC Cancer Research Centre, 675 10th Ave W, Vancouver, Vancouver, British Columbia, V5Z 1L3, Canada.
- BC Cancer Research Centre, 675 10th Ave W, Vancouver, British Columbia, V5Z 1L3, Canada.
- Department of Medical Physics, Iran University of Medical Sciences, Tehran, Tehran, 14496-14535, Iran (The Islamic Republic of).
- Tehran University of Medical Sciences, Vali-Asr Hospital, Tehran, Tehran, 1416753955, Iran (The Islamic Republic of).
- Tehran University of Medical Sciences, Tehran, Tehran, Tehran Province, 1416753955, Iran (The Islamic Republic of).
- BC Cancer Agency, 675 10th Ave W, Vancouver, British Columbia, V5Z 1G1, Canada.
- BC Cancer - Vancouver, 600 W 10th Ave, Vancouver, British Columbia, V5Z 4E6, Canada.
- BC Cancer Agency, 675 10th Ave W, Vancouver, British Columbia, V5Z 1L3, Canada.
- Molecular Oncology, BC Cancer Agency, 675 10th Ave W, Vancouver, British Columbia, V5Z 1L3, Canada.
- Radiology and Physics, The University of British Columbia, 675 10th Ave W, Vancouver, British Columbia, V5Z 1L3, Canada.
Abstract
Prostate-specific membrane antigen (PSMA) PET/CT is routinely used to restage prostate cancer (PCa) in patients with biochemical recurrence (BCR), yet negative scans may still harbor subclinical disease. This study investigated whether radiomics features extracted from recurrence-prone organs on negative [¹⁸F]DCFPyL PET/CT can predict clinical progression (CP) and clinical progression-free survival (CPFS).
Materials and Methods: We performed a post-hoc analysis of 132 patients with BCR (mean age, 74.5 years) who had negative [¹⁸F]DCFPyL PET/CT scans and received no further treatment after imaging. Recurrence-prone organs, defined as anatomical sites at highest risk for prostate cancer recurrence (prostate bed, lymph nodes, bones, liver, and lungs), were segmented using nnU-Net (TotalSegmentator), and radiomics features were extracted. Machine learning models (XGBoost) and Cox proportional hazards models were evaluated using nested cross-validation (5-fold outer, 3-fold inner). External validation across two independent centers was performed after ComBat harmonization. The effect of reader-assigned diagnostic certainty on predictive performance was also examined. Only recurrence-prone organs were analyzed, as prior studies have shown that more than 80% of PCa recurrences arise in these regions.
Results: Median PSA at imaging was 0.74 ng/mL. During a median follow-up of 25.5 months, 42 of 132 patients (31.8%) developed progression. The concordance index improved from 0.65 using clinical variables alone to 0.74 when PET, CT, and clinical features were combined (p < 0.05). Predictive performance was strongly influenced by diagnostic certainty, with moderate-certainty negative scans showing higher accuracy than high-certainty negative scans. Radiomics features derived from negative PSMA PET/CT reflected systemic recurrence risk and were associated with early lung metastases. External validation demonstrated less than 10% reduction in performance despite inter-center differences.
Conclusion: Radiomics signatures from recurrence-prone organs on negative PSMA PET/CT may reveal subclinical disease and provide complementary biomarkers for risk stratification in BCR patients.