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镓标记的P16-093(一种靶向前列腺特异性膜抗原的正电子发射断层显像放射性示踪剂)在前列腺癌中的初步评估

Preliminary Evaluation of Ga-P16-093, a PET Radiotracer Targeting Prostate-Specific Membrane Antigen in Prostate Cancer.

作者信息

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

机构信息

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.

出版信息

Mol Imaging Biol. 2022 Oct;24(5):710-720. doi: 10.1007/s11307-022-01720-6. Epub 2022 Mar 29.

Abstract

PURPOSE

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.

PROCEDURES

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.

RESULTS

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.

CONCLUSIONS

Based on its favorable imaging characteristics and diagnostic performance in prostate cancer, Ga-P16-093 PET/CT merits further investigation in larger clinical studies.

摘要

目的

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。

程序

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。

结果

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。

结论

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。

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