Abstract
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Introduction: The most common metastasis of prostate cancer (PCa) is bone metastasis. Skeletal-related event (SREs) can increase the risk of death in patients with PCa by 28%. 99Tcm-HYNIC-Glu-Urea-A (hereinafter referred to as: 99Tcm-PSMA) is a radionuclide labeled prostate-specific membrane antigen (PSMA) small molecular probe that can efficiently and specifically detect PCa lesions. The aim of our study was to investigate the difference between 99Tcm-PSMA SPECT/CT and 99Tcm-MDP SPECT/CT for the detection of bone metastasis in PCa.
Methods: A total 29 man who were pathologically confirmed PCa from October 2019 to February 2020 were prospectively enrolled in this study and gave informed consent under the guidance of the Ethics Board of Fujian Provincial Hospital. The median age was 69 (range, 61-87) years. The median PSA level was 2.15 (range, 0.003-906.2) ng/ml. They all underwent both99Tcm-PSMA SPECT/CT and 99Tcm-MDP SPECT/CT (Discovery NM/CT 670, with low energy high resolution collimators) at an average interval of 12.1days (at least 1 day). They did not receive any antineoplastic therapy during the two intervals. According to the examination results, they were divided into bone metastasis group and non-bone metastasis group. For all 29 patients, the positive and negative cases of bone metastasis diagnosed by the two methods were counted, and the diagnostic efficacy of the two methods were compared. The detected bone lesions were divided and scored according to specific anatomical areas, and according to the concentration of imaging agents and anatomical manifestations, it can be divided into "typical metastasis" and "equivocal metastasis". To analyze the uptake degree and difference of 99Tcm-PSMA and 99Tcm -MDP in bone lesions. Based on per bone lesion, the differences of the number of bone lesions detected by the two methods under different Gleason scores and PSA levels were compared.
Results: Among the 29 patients, 11 cases were diagnosed as bone metastasis and 18 cases without bone metastasis. For all 29 patients, there was no significant difference in the detection rate of bone metastases between the two methods (Kappa=0.590, P=0.219). The sensitivity of 99Tcm-PSMA SPECT/CT and 99Tcm-MDP SPECT/CT for the detection of bone metastasis was 100% and 90.9%, respectively, and there was no significant difference between them (P=1.0), but the specificity of 99Tcm-PSMA SPECT/CT was significantly higher than that of 99Tcm-MDP SPECT/CT (100% vs 72.8%, P=0.045). Based on per bone lesion, there was no significant difference in the concentration of 99Tcm-PSMA and 99Tcm -MDP in bone lesions(P=0.266,Z=-1.192); The proportion of "typical metastasis" and "equivocal metastasis" detected by the two methods was 6.4 (PSMA) and 1.3 (MDP) ,respectively. Under different PSA levels and Gleason scores, there was no significant difference in the number of bone lesions (1, 2, 3, 4, 5, > 5) detected by the two methods. However, in the follow-up, the number of false positives of bone lesions detected by 99Tcm-MDP SPECT/CT was more than that of 99Tcm-PSMA SPECT/CT(MDP,15 vs PSMA,0), and the 20 true positive bone lesions detected in 99Tcm-PSMA SPECT/CT were not detected in 99Tcm-MDP SPECT/CT.
Conclusions: The sensitivity of 99Tcm-PSMA SPECT/CT in the diagnosis of PCa bone metastasis was slightly higher than that of 99Tcm-MDP SPECT/CT, but there was no statistical difference. The specificity of 99Tcm-PSMA SPECT/CT in the diagnosis of bone metastasis of PCa is significantly better than that of 99Tcm-MDP SPECT/CT, and it can clearly diagnose the nature of bone lesions, and the diagnostic efficiency is higher than that of 99Tcm-MDP SPECT/CT. Because 99Tcm-PSMA SPECT/CT also has the function of specific diagnosis of PCa related lesions, it will have a wide application prospect.