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Comparative Evaluation of ( 18 F)AlF-PSMA-HBED-CC and 68 Ga-PSMA-HBED-CC in Staging Intermediate-/High-Risk Prostate
Gerardo Gabriel Dos Santos Loureiro1,2, Pablo Duarte Couto1, Juan Pablo Gambini Gonzalez1,2
1Uruguayan Centre of Molecular Imaging (CUDIM), Montevideo, Uruguay.
Abstract:
Objective 68 Ga-PSMA-HBED-CC positron emission tomography (PET)/computed tomography (CT) represents a clinically relevant technique for the evaluation of prostate cancer (PCa) patients, whereas 18 F-AIF-PSMA-HBED-CC is a novel tracer produced in our center, with suitable radiochemical purity for clinical purposes. We prospectively compared the diagnostic values of both tracers for the detection of metastatic disease in patients with intermediate-/high-risk PCa at initial staging. Materials and Methods Sixty-six patients (mean age: 63 years; range: 52-78 years) with PCa at initial staging (Gleason score ≥6; median prostate-specific antigen [PSA]: 10 ng/mL; range:1.7-152 ng/mL) prospectively underwent routine 68 Ga-PSMA-11 and 18 F-AlF-PSMA-11 PET/CT scanning with a 64-slice PET/CT scan with time-of-flight (TOF) correction. We measured the maximum standardized uptake value (SUVmax) and lesion-to-background ratio (LBR) in all coincidentally detected lesions. Open prostatectomy and pelvic lymph node dissection were performed in nonmetastatic patients. Histopathology, correlative imaging, and/or clinical follow-up were considered the gold standard. Follow-up was conducted at least 4 months after PET/CT scanning (median: 6.4 months; range: 4-11 months). Sensitivity, specificity, and predictive values were calculated. Results The overall detection rate was 85% (56/66) for both tracers. At least one suspicious lesion indicating potential PCa metastasis was detected in 20 (30%) and 21 (32%) of 66 patients for 68 Ga-PSMA-11 and 18 F-AIF-PSMA-11 tracers, respectively. A total of 145 extra-prostatic lesions were detected in the bone ( n = 56), lymph nodes ( n = 88), and lung ( n = 1) by at least one radiopharmaceutical: 131 (90%) for 68 Ga-PSMA-11 and 123 (85%) for 18 F-AlF-PSMA-11. In concordant lesions, a significant correlation was found between the SUVmax of both tracers ( r = 0.90, p = 0.001). The SUVmax and LBR for 18 F-AlF-PSMA-11 were higher in bone foci ( n = 39) compared with 68 Ga-PSMA-11 (7.2 vs. 8.9 and 14 vs. 13, respectively, p = 0.02). For the detection of systemic metastasis, the sensitivity values were the same for both techniques: 0.90 (95% confidence interval [CI]: 0.68-0.98). We calculated specificities of 0.96 (95% CI: 0.85-0.99) and 0.94 (95% CI: 0.82-0.98) for 68 Ga-PSMA-11 and 18 F-AlF-PSMA-11, respectively. Conclusions 68 Ga-PSMA-11 and 18 F-AlF-PSMA-11 PET/CT seem to be clinically equivalent imaging techniques for the assessment of primary intermediate-/high-risk PCa with promising potential for the detection of metastatic spread that would impact patient management.
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