From the Departments of Nuclear Medicine.
Urology.
Clin Nucl Med. 2023 Jan 1;48(1):e1-e8. doi: 10.1097/RLU.0000000000004430. Epub 2022 Oct 14.
This study aimed to compare 18 F-PSMA-1007 PET/CT with 68 Ga-PSMA-11 PET/CT for initial staging in intermediate- and high-risk prostate cancer (PCa) patients.
Forty treatment-naive, biopsy-proven, intermediate- or high-risk PCa patients were prospectively recruited. Each patient underwent PET/CT with 68 Ga-PSMA-11 and 18 F-PSMA-1007 (within 2 weeks). Assessment of both set of images included delineating number and characteristics of lesions, measurement of tracer uptake (SUV max ), miPSMA scoring, and PET-based stage categorization.
Intraprostatic lesions were detected in all patients by both tracers with concordant PET-based T stage. Median SUV max of the dominant PSMA-positive prostatic lesions was not significantly different with 18 F-PSMA-1007 and 68 Ga-PSMA-11 (19.9 vs 19.4, P = 0.127, n = 40). Prostatic miPSMA scores were similar in 31/40 (77.5%) patients with both tracers (weighted κ = 0.71). In 23/40 (57.5%) patients, regional lymph nodes (n = 171) were detected by both tracers. Few additional PET-positive regional lymph nodes (n = 3) were exclusively detected by 18 F-PSMA in 2 patients without altering PET-based N stage. Extraregional lymph nodes (n = 123 in 17/40 patients) and visceral metastatic lesions (n = 18 in 3/40 patients) were detected concordantly by both tracers. PET-positive marrow based and skeletal metastases (n = 71) were detected in 14/40 (35%) patients by both tracers. Few additional marrow and skeletal lesions (n = 7) were exclusively detected on 18 F-PSMA-1007 in 5/14 patients, potentially upstaging PET-based M stage in 2/5 patients. Both radiotracers showed excellent interreader agreement for region-wise detection of lesions.
Our results suggest that 18 F-PSMA-1007 PET/CT is comparable to 68 Ga-PSMA-11 PET/CT in detecting primary and metastatic lesions of PCa.
本研究旨在比较 18 F-PSMA-1007 PET/CT 和 68 Ga-PSMA-11 PET/CT 在中高危前列腺癌(PCa)患者中的初始分期。
前瞻性招募了 40 名未经治疗、经活检证实的中高危 PCa 患者。每位患者均接受了 68 Ga-PSMA-11 和 18 F-PSMA-1007 的 PET/CT(2 周内)。对两组图像的评估均包括病灶数量和特征的描绘、示踪剂摄取(SUVmax)的测量、miPSMA 评分和基于 PET 的分期分类。
两种示踪剂均能在所有患者的前列腺内病灶中检出,且基于 PET 的 T 分期具有一致性。40 例患者中,18 F-PSMA-1007 和 68 Ga-PSMA-11 检测到的优势 PSMA 阳性前列腺病灶的中位 SUVmax 无显著差异(19.9 比 19.4,P=0.127,n=40)。在 31/40(77.5%)名患者中,两种示踪剂的前列腺 miPSMA 评分相似(加权κ=0.71)。在 23/40(57.5%)名患者中,两种示踪剂均能检测到区域淋巴结(n=171)。在 2 名患者中,18 F-PSMA 还额外检测到了少数(n=3)仅 PET 阳性的区域淋巴结,这并未改变基于 PET 的 N 分期。在 17/40 名患者中,两种示踪剂还均能检测到额外的区域外淋巴结(n=123)和内脏转移病灶(n=18)。在 40 名患者中的 14 名(35%)患者中,两种示踪剂均能检测到骨髓和骨骼的 PET 阳性转移病灶(n=71)。在 5 名患者中(2/5),18 F-PSMA-1007 还额外检测到了少数(n=7)骨髓和骨骼病灶,这可能使 2 名患者的基于 PET 的 M 分期上调。两种示踪剂在区域病灶检测方面均具有良好的观察者间一致性。
我们的结果表明,18 F-PSMA-1007 PET/CT 与 68 Ga-PSMA-11 PET/CT 在检测 PCa 的原发性和转移性病灶方面具有可比性。