Nuclear medicine communications · 2026
Prognostic value of preoperative gallium-68 prostate-specific membrane antigen PET/computed tomography in predicting biochemical recurrence after radical prostatectomy.
СтатьяНазвание и аннотация: Перевод в очереди
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Durak Hüseyin Mert, Sanci Adem, Hepşen Emre, Yiğman Metin, Çinar Alev, Sağnak Azmi Levent, Karakoyunlu Ahmet Nihat
Аннотация
OBJECTIVES: This study evaluated the prognostic value of intraprostatic maximum standardized uptake value (SUV max ) on primary-staging gallium-68 prostate-specific membrane antigen ( 68 Ga-PSMA) PET/computed tomography for predicting biochemical recurrence (BCR) and BCR-free survival after margin-negative radical prostatectomy, and explored an SUV max cutoff.
METHODS: This retrospective study included 78 men (2023-2024) who underwent preoperative 68 Ga-PSMA PET/computed tomography, all reevaluated by an experienced nuclear medicine physician. BCR was defined as prostate-specific antigen at least 0.2 ng/ml on two consecutive tests. Follow up duration and time to recurrence were recorded. Mann-Whitney U, χ 2 , receiver operating characteristic, Kaplan-Meier, and Cox regression analyses were performed.
RESULTS: BCR occurred in 21 of 78 patients (26.9%). Median follow up was 18 months, and median time to BCR was 12 months. Intraprostatic SUV max was significantly higher in patients with BCR ( P < 0.001). Receiver operating characteristic analysis showed an area under the curve of 0.798; the exploratory cutoff was 12.8, with 71.4% sensitivity and 84.2% specificity. Kaplan-Meier analysis showed significantly worse BCR-free survival in patients with SUV max at least 12.8 (log-rank P < 0.001). In univariable Cox analysis, each 1-unit increase in SUV max was associated with higher BCR risk (hazard ratio = 1.11, 95% confidence interval 1.06-1.16, P < 0.001), and this association remained significant in limited multivariable models.
CONCLUSIONS: Intraprostatic SUV max appears to be an exploratory imaging biomarker associated with postoperative BCR and shorter BCR-free survival rather than a stand-alone prognostic determinant. Larger prospective multicenter studies are needed for validation.
METHODS: This retrospective study included 78 men (2023-2024) who underwent preoperative 68 Ga-PSMA PET/computed tomography, all reevaluated by an experienced nuclear medicine physician. BCR was defined as prostate-specific antigen at least 0.2 ng/ml on two consecutive tests. Follow up duration and time to recurrence were recorded. Mann-Whitney U, χ 2 , receiver operating characteristic, Kaplan-Meier, and Cox regression analyses were performed.
RESULTS: BCR occurred in 21 of 78 patients (26.9%). Median follow up was 18 months, and median time to BCR was 12 months. Intraprostatic SUV max was significantly higher in patients with BCR ( P < 0.001). Receiver operating characteristic analysis showed an area under the curve of 0.798; the exploratory cutoff was 12.8, with 71.4% sensitivity and 84.2% specificity. Kaplan-Meier analysis showed significantly worse BCR-free survival in patients with SUV max at least 12.8 (log-rank P < 0.001). In univariable Cox analysis, each 1-unit increase in SUV max was associated with higher BCR risk (hazard ratio = 1.11, 95% confidence interval 1.06-1.16, P < 0.001), and this association remained significant in limited multivariable models.
CONCLUSIONS: Intraprostatic SUV max appears to be an exploratory imaging biomarker associated with postoperative BCR and shorter BCR-free survival rather than a stand-alone prognostic determinant. Larger prospective multicenter studies are needed for validation.