Lee Hwan, Scheuermann Joshua S, Young Anthony J, Doot Robert K, Daube-Witherspoon Margaret E, Schubert Erin K, Fillare Matthew A, Alexoff David, Karp Joel S, Kung Hank F, Pryma Daniel A
Department of Radiology, University of Pennsylvania Perelman School of Medicine, 3400 Spruce Street, Philadelphia, PA, 19104, USA.
Five Eleven Pharma Inc., Philadelphia, PA, 19104, USA.
Mol Imaging Biol. 2022 Oct;24(5):710-720. doi: 10.1007/s11307-022-01720-6. Epub 2022 Mar 29.
Prostate-specific membrane antigen (PSMA) is a promising molecular target for imaging of prostate adenocarcinoma. Ga-P16-093, a small molecule PSMA ligand, previously showed equivalent diagnostic performance compared to Ga-PSMA-11 PET/CT in a pilot study of prostate cancer patients with biochemical recurrence (BCR). We performed a pilot study for further characterization of Ga-P16-093 including comparison to conventional imaging.
Patients were enrolled into two cohorts. The biodistribution cohort included 8 treated prostate cancer patients without recurrence, who underwent 6 whole body PET/CT scans with urine sampling for dosimetry using OLINDA/EXM. The dynamic cohort included 15 patients with BCR and 2 patients with primary prostate cancer. Two patients with renal cell carcinoma were also enrolled for exploratory use. A dynamic PET/CT was followed by 2 whole body scans for imaging protocol optimization based on bootstrapped replicates. Ga-P16-093 PET/CT was compared for diagnostic performance against available F-fluciclovine PET/CT, Tc-MDP scintigraphy, diagnostic CT, and MRI.
Ga-P16-093 deposited similar effective dose (0.024 mSv/MBq) and lower urinary bladder dose (0.064 mSv/MBq) compared to Ga-PSMA-11. The kidneys were the critical organ (0.290 mSv/MBq). While higher injected activities were preferable, lower injected activities at 74-111 MBq (2-3 mCi) yielded 80% retention in signal-to-noise ratio. The optimal injection-to-scan interval was 60 min, with acceptable delay up to 90 min. Ga-P16-093 PET/CT showed superior diagnostic performance over conventional imaging with overall patient-level lesion detection rate of 71%, leading to a change in management in 42% of the patients.
Based on its favorable imaging characteristics and diagnostic performance in prostate cancer, Ga-P16-093 PET/CT merits further investigation in larger clinical studies.
前列腺特异性膜抗原(PSMA)是前列腺腺癌成像的一个有前景的分子靶点。Ga-P16-093是一种小分子PSMA配体,在一项针对生化复发(BCR)前列腺癌患者的初步研究中,其诊断性能先前显示与Ga-PSMA-11 PET/CT相当。我们进行了一项初步研究,以进一步表征Ga-P16-093,包括与传统成像进行比较。
患者被纳入两个队列。生物分布队列包括8例未复发的接受治疗的前列腺癌患者,他们接受了6次全身PET/CT扫描,并使用OLINDA/EXM进行尿液采样以进行剂量测定。动态队列包括15例BCR患者和2例原发性前列腺癌患者。还纳入了2例肾细胞癌患者用于探索性研究。在动态PET/CT之后进行2次全身扫描,以基于自展重复进行成像方案优化。将Ga-P16-093 PET/CT的诊断性能与现有的F-氟代脱氧胸苷PET/CT、Tc-MDP闪烁显像、诊断性CT和MRI进行比较。
与Ga-PSMA-11相比,Ga-P16-093的有效剂量(0.024 mSv/MBq)相似,膀胱剂量较低(0.064 mSv/MBq)。肾脏是关键器官(0.290 mSv/MBq)。虽然较高的注射活度更可取,但74-111 MBq(2-3 mCi)的较低注射活度可使信噪比保持80%。最佳注射至扫描间隔为60分钟,延迟至90分钟仍可接受。Ga-P16-093 PET/CT在诊断性能上优于传统成像,总体患者层面的病变检测率为71%,导致42%的患者治疗方案改变。
基于其在前列腺癌中良好的成像特征和诊断性能,Ga-P16-093 PET/CT值得在更大规模的临床研究中进一步研究。