Nodal maximum standardised uptake value improves PSMA-PET/CT-based nodal staging in intermediate- and high-risk prostate cancer.
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Bruins Slot Alexandra S, Sweere Vera, Heetman Joris G, Hermsen Rick, Wever Lieke, Lavalaye Jules, Vinken Maarten, Bahler Clinton D, Tann Mark, Kesch Claudia, Telli Tugce, Fendler Wolfgang P, Chiu Peter Ka-Fung, Wu Kwan Kit, Zattoni Fabio, Evangelista Laura, Ceci Francesco, Miszczyk Marcin, Rajwa Pawel, Matsukawa Akihiro, Fazekas Tamás, Barletta Francesco, Briganti Alberto, Montorsi Francesco, Gandaglia Giorgio, Van Basten Jean-Paul A, Van Melick Harm H E, Van den Bergh Roderick C N, Marra Giancarlo, Soeterik Timo F W, Scheltema Matthijs J V, European Association of Urology‐Young Academic Urologists (EAU‐YAU) Prostate Cancer Working Group
Аннотация
PATIENTS AND METHODS: This international multicentre study included patients with histopathologically confirmed PCa who underwent preoperative PSMA-PET and robot-assisted radical prostatectomy with extended pelvic lymph node dissection (2016-2023). Sensitivity, specificity, PPV, and negative predictive value (NPV) for LNI detection were calculated, defining a positive test as non-physiological PSMA uptake classified according to the Prostate Cancer Molecular Imaging Standardised Evaluation (PROMISE) molecular imaging Tumour-Node-Metastasis (miTNM) system. Receiver operating curves analysis identified optimal nodal SUVmax cut-offs for pelvic LNI. Logistic regression assessed predictors for pathological N1 stage (pN1) and high-volume nodal disease (four or more positive nodes). Clinical decision tools were developed to stratify patients into three risk groups for pN1 and high-volume nodal disease.
RESULTS: A total of 521 patients were included, with a median (interquartile range) age of 66 (61-71) years and prostate-specific antigen (PSA) level of 9.9 (6.6-17.0) ng/mL. The PSMA-PET showed 45.0% sensitivity, 94.3% specificity, 64.7% PPV, and 88.3% NPV for LNI detection. Adding nodal SUVmax ≥4.9 improved the PPV to 81.1% and sensitivity to 71.4% and, combined with a PSA level ≥10 ng/mL, magnetic resonance imaging (MRI) T-stage ≥T3a, and miT-stage ≥T3a, identified 95% of pN1 cases in the high-risk group. High-volume nodal disease was found in 3.8%, including 1.1% in miN0 patients. Nodal SUVmax ≥7.2, MRI T-stage ≥T3a, and miN2 (multiple suspicious LNs) were predictors for high-volume nodal disease and, combined in a clinical decision tool, excluded all low-risk patients for high-volume nodal disease.
CONCLUSION: Nodal SUVmax improves PPV of PSMA-PET for nodal staging and aids in excluding high-volume nodal disease. Clinical decision tools integrating nodal SUVmax with relevant clinical parameters demonstrate potential to guide individualised nodal management. These findings warrant external validation in larger cohorts.