Werner P, Neumann C, Eiber M, Wester H J, Schottelius M
Nuclear Medicine Neumann, Outpatient Practice for Nuclear Medicine, Leipzig, Germany.
Department of Nuclear Medicine, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.
EJNMMI Res. 2020 May 7;10(1):45. doi: 10.1186/s13550-020-00635-z.
Prostate-specific membrane antigen (PSMA) SPECT imaging in prostate cancer (PCa) could be a valuable alternative in regions where access to PSMA-PET imaging is restricted. [Tc]Tc-PSMA-I&S is a new Tc-labeled PSMA-targeting SPECT agent, initially developed for radio-guided surgery. We report on the diagnostic use of [Tc]Tc-PSMA-I&S-SPECT/CT in PCa.
[Tc]Tc-PSMA-I&S-SPECT/CT was performed and evaluated in 210 outpatients with PCa at a single center. Patients were imaged for biochemical recurrence (BCR, n = 152, mean PSA 8.7 ng/ml), for primary staging of high-risk PCa (n = 12, mean PSA 393 ng/ml), and restaging in advanced recurrent PCa (n = 46, mean PSA 101.3 ng/ml). Number and location of positive lesions were determined for the different subgroups. For BCR, detection rates were calculated, defined as the proportion of scans with at least one PSMA-positive lesion. PSMA positive lesions were detected in 65.2% of all 210 patients. Tumor tissue was mainly detected in lymph nodes (59%), in the bone (42%), and in the prostate (fossa) (28%). In the subgroup of patients referred for detection of BCR the detection rate increased from 20% at a PSA level < 1 ng/ml to 82.9% and 100% at PSA levels > 4 ng/ml and > 10 ng/ml, respectively. In the subgroup of high-risk patients referred for primary staging, 42% demonstrated metastatic disease. Restaging of advanced recurrent PCa revealed detectability of PSMA positive tumor lesions in 85% of the scans.
[Tc]Tc-PSMA-I&S-SPECT/CT was useful in PSMA-targeted imaging of PCa at various clinical stages. At low PSA levels (< 4 ng/ml), detection rates of [Tc]Tc-PSMA-I&S-SPECT/CT in BCR are clearly inferior to data reported for PET-imaging and should thus only be considered for lesion detection if imaging with PET is unavailable. However, at higher PSA levels (> 4 ng/ml) [Tc]Tc-PSMA-I&S-SPECT/CT provides high detection rates in BCR. [Tc]Tc-PSMA-I&S-SPECT/CT can also be used for primary staging and for restaging of advanced recurrent PCa. However, further studies are needed to assess the clinical value in these indications.
在前列腺癌(PCa)中,前列腺特异性膜抗原(PSMA)单光子发射计算机断层扫描(SPECT)成像在那些获取PSMA正电子发射断层扫描(PET)成像受限的地区可能是一种有价值的替代方法。[锝(Tc)]Tc-PSMA-I&S是一种新的锝标记的靶向PSMA的SPECT显像剂,最初是为放射性引导手术而开发的。我们报告了[锝(Tc)]Tc-PSMA-I&S-SPECT/CT在PCa诊断中的应用。
在一个中心对210例PCa门诊患者进行了[锝(Tc)]Tc-PSMA-I&S-SPECT/CT检查并进行评估。对患者进行成像以评估生化复发(BCR,n = 152,平均前列腺特异性抗原[PSA] 8.7 ng/ml)、高危PCa的初始分期(n = 12,平均PSA 393 ng/ml)以及晚期复发性PCa的再分期(n = 46,平均PSA 101.3 ng/ml)。确定了不同亚组中阳性病变的数量和位置。对于BCR,计算了检测率,定义为至少有一个PSMA阳性病变的扫描比例。在所有210例患者中,65.2%检测到PSMA阳性病变。肿瘤组织主要在淋巴结(59%)、骨骼(42%)和前列腺(前列腺窝)(28%)中被检测到。在因检测BCR而转诊的患者亚组中,检测率从PSA水平<1 ng/ml时的20%分别增至PSA水平>4 ng/ml和>10 ng/ml时的82.9%和100%。在因初始分期而转诊的高危患者亚组中,42%显示有转移性疾病。晚期复发性PCa的再分期显示,85%的扫描中可检测到PSMA阳性肿瘤病变。
[锝(Tc)]Tc-PSMA-I&S-SPECT/CT在PCa不同临床分期的PSMA靶向成像中是有用的。在低PSA水平(<4 ng/ml)时,[锝(Tc)]Tc-PSMA-I&S-SPECT/CT在BCR中的检测率明显低于PET成像报告的数据,因此只有在无法进行PET成像时才应考虑用于病变检测。然而,在较高PSA水平(>4 ng/ml)时,[锝(Tc)]Tc-PSMA-I&S-SPECT/CT在BCR中提供了高检测率。[锝(Tc)]Tc-PSMA-I&S-SPECT/CT也可用于初始分期以及晚期复发性PCa的再分期。然而,需要进一步研究来评估这些适应证的临床价值。