Doot Robert K, Young Anthony J, Daube-Witherspoon Margaret E, Alexoff David, Labban Kyle J, Lee Hwan, Wu Zehui, Zha Zhihao, Choi Seok R, Ploessl Karl H, Schubert Erin K, Lee Hsiaoju, Zhu Lin, Reddin Janet S, Karp Joel S, Kung Hank, Pryma Daniel A
Department of Radiology, University of Pennsylvania, Philadelphia, PA 19104, United States of America.
Department of Radiology, University of Pennsylvania, Philadelphia, PA 19104, United States of America.
Nucl Med Biol. 2020 Jul-Aug;86-87:1-8. doi: 10.1016/j.nucmedbio.2020.04.002. Epub 2020 Apr 20.
[Ga]Ga-P15-041 ([Ga]Ga-HBED-CC-BP) is a novel bone-seeking PET radiotracer that can be generator-produced. We undertook a Phase 0/I clinical trial to assess its potential for imaging bone metastases in prostate cancer including assessment of radiotracer biodistribution and dosimetry.
Subjects with prostate cancer and known or suspected osseous metastatic disease were enrolled into one of two arms: dosimetry or dynamic. Dosimetry was performed with 6 whole body PET acquisitions and urine collection spanning 3 h; normal organ dosimetry was calculated using OLINDA/EXM. Dynamic imaging included a 60 min acquisition over a site of known or suspected disease followed by two whole body scans. Bootstrapping and subsampling of the acquired list-mode data were conducted to recommend image acquisition parameters for future clinical trials.
Up to 233 MBq (6.3 mCi) of [Ga]Ga-P15-041 was injected into 12 enrolled volunteers, 8 in dosimetry and 4 in dynamic cohorts. Radiotracer accumulated in known bone lesions and cleared rapidly from blood and soft tissue. The highest individual organ dose was 0.135 mSv/MBq in the urinary bladder wall. The average effective dose was 0.0173 ± 0.0036 mSv/MBq. An average injected activity of 166.5 MBq (4.5 mCi) resulted in absorbed dose estimates of 22.5 mSv to the urinary bladder wall, 8.2 mSv to the kidneys, and an effective dose of 2.9 mSv. Lesion signal to noise ratios on images generated from subsampled data were significantly higher for injected activities above 74 MBq (2 mCi) and were also significantly higher for imaging at 90 min than at 180 min post-injection.
Dosimetry estimates are acceptable and [Ga]Ga-P15-041 uptake characteristics in patients with confirmed bone metastases support its continued development.
Use of [Ga]Ga-P15-041 would not require cyclotron infrastructure for manufacturing and distribution, allowing for improved patient access to a promising PET bone imaging agent.
[镓]Ga-P15-041([镓]Ga-HBED-CC-BP)是一种新型的骨靶向正电子发射断层显像(PET)放射性示踪剂,可通过放射性核素发生器生产。我们开展了一项0/Ⅰ期临床试验,以评估其对前列腺癌骨转移灶成像的潜力,包括评估放射性示踪剂的生物分布和剂量测定。
患有前列腺癌且已知或疑似存在骨转移疾病的受试者被纳入两个研究组之一:剂量测定组或动态成像组。剂量测定通过6次全身PET采集和3小时尿液收集来进行;使用OLINDA/EXM计算正常器官的剂量。动态成像包括对已知或疑似疾病部位进行60分钟的采集,随后进行两次全身扫描。对采集的列表模式数据进行自抽样和二次抽样,以推荐未来临床试验的图像采集参数。
向12名入组志愿者注射了高达233MBq(6.3mCi)的[镓]Ga-P15-041,其中8人在剂量测定组,4人在动态成像组。放射性示踪剂在已知的骨病变中蓄积,并迅速从血液和软组织中清除。膀胱壁的最高个体器官剂量为0.135mSv/MBq。平均有效剂量为0.0173±0.0036mSv/MBq。平均注射活度为166.5MBq(4.5mCi)时,膀胱壁的吸收剂量估计为22.5mSv,肾脏为8.2mSv,有效剂量为2.9mSv。对于注射活度高于74MBq(2mCi)的情况,二次抽样数据生成的图像上的病变信噪比显著更高,并且在注射后90分钟成像时的信噪比也显著高于180分钟时。
剂量测定估计值是可接受的,[镓]Ga-P15-041在确诊骨转移患者中的摄取特征支持其继续研发。
使用[镓]Ga-P15-041不需要回旋加速器基础设施来进行生产和配送,从而使患者能够更容易获得一种有前景的PET骨显像剂。