Hoffmann Manuela A, Miederer Matthias, Wieler Helmut J, Ruf Christian, Jakobs Frank M, Schreckenberger Mathias
Supervisory Center for Medical Radiation Protection, Bundeswehr Medical Service Headquarters, Koblenz, Germany.
Department of Nuclear Medicine, Johannes Gutenberg-University, Mainz, Germany.
Oncotarget. 2017 Nov 14;8(67):111073-111083. doi: 10.18632/oncotarget.22441. eCollection 2017 Dec 19.
Radiolabeled prostate-specific membrane antigen (PSMA) has proven to be a highly accurate method to detect recurrence and metastases of prostate cancer, but only sparse data is available about its performance in the diagnosis of clinically significant primary prostate cancer.
We compared Ga-PSMA-11 PET/CT in 25 patients with FEC PET/CT in 40 patients with suspected prostate carcinoma based on an increased PSA level.The PET/CT results were compared with the histopathologic Gleason Score (GS) of biopsies.
The Ga-PSMA-11 PET/CT revealed highly suspect prostatic lesions (maximum standardized uptake value/SUV >2.5) in 21/25 patients (84%), associated with GS≥6 (low-grade/high-grade carcinoma). Two histopathologic non-malignancy-relevant cases (GS<6) had PSMA-SUV ≤2.5; all histopathologic high-grade cases (GS≥7b) showed PSMA-SUV >12.0 which further increased with rising GS. There were 2 false positives and no false negative findings for high-grade prostate cancer using a cut off-level for SUV of 2.5.In contrast, the FEC PET/CT showed suspected malignant lesions in 38/40 patients (95%), which included 3 lesions with GS<6. The mean SUV values did not differ with different GS. There were 11 false positives and 1 false negative for detection of high-grade prostate cancer (cut off 2.5).By means of ROC analysis a SUV of 5.4 was found to be an optimal cut off-level to distinguish between low- and high-grade carcinoma in Ga-PSMA-11 PET/CT (AUC=0.9692; 95% CI 0.9086;1.0000;SD(AUC)=0.0309)). Choosing a cut off-level of SUV5.4, Ga-PSMA-11 PET/CT was able to distinguish between GS ≤7a/≥7b with a sensitivity of 84%, a specificity of 100%, a negative predictive value (NPV) of 67%, and an efficiency of 88% (<0.001).The ROC analysis revealed a SUV 6.5 as an optimal cut off-level to distinguish between low- and high-grade carcinoma in FEC PET/CT (AUC=0.7470; 95% CI 0.5919;0.9020;SD(AUC)=0.0791) with a sensitivity of 61% and a specificity of 92%; but the efficiency was only 70% and the NPV 50% (=0.01).
Ga-PSMA-11 PET/CT guided biopsy of the prostate increases diagnostic precision and is likely to help to reduce overtreatment of low-grade malignant disease as well as detect the foci of the highest Gleason pattern. Both methods (Ga-PSMA-11,FEC) were suitable to detect primary prostate cancer, but the excellent image quality, the higher specificity and the good correlation of positive scans with GS are advantages of Ga-PSMA-11.
放射性标记的前列腺特异性膜抗原(PSMA)已被证明是检测前列腺癌复发和转移的一种高度准确的方法,但关于其在诊断具有临床意义的原发性前列腺癌中的表现仅有少量数据。
我们对25例患者进行了镓 - PSMA - 11 PET/CT检查,并对40例基于前列腺特异抗原(PSA)水平升高而怀疑患有前列腺癌的患者进行了氟乙基半胱氨酸(FEC)PET/CT检查。将PET/CT结果与活检的组织病理学Gleason评分(GS)进行比较。
镓 - PSMA - 11 PET/CT在21/25例患者(84%)中发现了高度可疑的前列腺病变(最大标准化摄取值/SUV >2.5),与GS≥6(低级别/高级别癌)相关。2例组织病理学上与恶性无关的病例(GS<6)的PSMA - SUV≤2.5;所有组织病理学高级别病例(GS≥7b)的PSMA - SUV>12.0,且随着GS升高进一步增加。对于高级别前列腺癌,使用SUV截止值2.5时,有2例假阳性,无假阴性结果。相比之下,FEC PET/CT在38/40例患者(95%)中发现了可疑恶性病变,其中包括3例GS<6的病变。不同GS的平均SUV值无差异。对于高级别前列腺癌的检测(截止值2.5),有11例假阳性和1例假阴性。通过ROC分析发现,在镓 - PSMA - 11 PET/CT中,SUV为5.4是区分低级别和高级别癌的最佳截止值(AUC = 0.9692;95%CI 0.9086;1.0000;SD(AUC)=0.0309))。选择SUV 5.4的截止值时,镓 - PSMA - 11 PET/CT能够以84%的敏感性、100%的特异性、67%的阴性预测值和88%的效率区分GS≤7a/≥7b(<0.001)。ROC分析显示,在FEC PET/CT中,SUV 6.5是区分低级别和高级别癌的最佳截止值(AUC = 0.7470;95%CI 0.5919;0.9020;SD(AUC)=0.0791)),敏感性为61%,特异性为92%;但效率仅为70%,阴性预测值为50%(=0.01)。
镓 - PSMA - 11 PET/CT引导下的前列腺活检提高了诊断准确性,可能有助于减少低级别恶性疾病的过度治疗,并检测出最高Gleason分级模式的病灶。两种方法(镓 - PSMA - 11、FEC)都适用于检测原发性前列腺癌,但镓 - PSMA - 11具有出色的图像质量、更高的特异性以及阳性扫描与GS的良好相关性。