前列腺癌症复发的18F-MD-PSMA(多剂量PMSA显像剂)PET/CT:回顾性试验结果。

IF 1.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Hongliang Fu, Sheng Liang, Miaomiao Xu, Jun Guo, Qiang Liu, Jian Kang, Linlin Zhang, Zihao Liu, Lin Ding, Yufei Ma, Bin Yang, Xudong Yao, Jun Qi, Hui Wang, Yongquan Cai
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引用次数: 0

摘要

目的:本研究旨在评估18F-MD-PSMA PET/CT在以前通过手术或治疗前列腺癌症但后来通过生化方法复发的患者中的表现。方法:这项回顾性研究按顺序纳入213名患者,他们之前曾接受过前列腺癌症的手术或治疗,但后来PSA复发。在这213名患者中,共有191人被纳入本分析。所有患者在根治性前列腺切除术或治疗后均出现生化复发,在1周内进行了18F-MD-PSMA PET/CT扫描,扫描时未进行激素治疗。将新的示踪剂与11C胆碱直接进行敏感性比较。结果:在3例患者中,对18F-MD-PSMA和11C胆碱进行了并排比较,发现前者的敏感性是后者的3倍左右。对191名复发患者使用18F-MD-PSMA进行的PET成像分析显示,只有不到10%的患者显示疾病局限于前列腺。在远处病变中,数量按顺序递减的是骨骼,其次是淋巴结和其他器官。每个患者病变中的最大SUV呈指数衰减,SUV向下端倾斜。诊断时测量的Gleason评分与每位患者的平均病变数量、该患者队列中的平均最大SUV值以及PET成像时测量的PSA值没有相关性。在每个患者中观察到的病变数量与PET成像时测量的PSA值没有相关性。当在PET成像时测量PSA值作为独立的生物标志物时,使用18F-MD-PSMA的PET成像的阳性率随着PSA值的增加而增加,但PSMA表达低或阴性的情况除外。从这种放射性配体的PET成像来看,大多数患者表现出寡转移,倾向于使用局部治疗来控制疾病。结论:18F-MD-PSMA作为一种放射性配体,在既往治疗后出现生化复发的患者中优于11C胆碱。它的PET成像结果与已建立的PSMA放射性配体的结果相匹配,但发现它的化学结构增加了与其他功能分子结合的特征,例如具有治疗特性的分子。这个放射性配体为我们的进一步工作奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An 18F-MD-PSMA (Multi-dentate PMSA Imaging Agent) PET/CT in Prostate Cancer Relapse: Results of a Retrospective Trial.

Purpose: This study aimed to evaluate the performance of 18F-MD-PSMA PET/CT in patients previously treated for prostate cancer by either surgery or therapy, but later relapsed biochemically.

Methods: This retrospective study enrolled 213 patients in sequence previously treated for prostate cancer by either surgery or therapy, but later PSA relapsed. A total of 191 of these 213 patients were included in this analysis. All patients were biochemically relapsed after radical prostatectomy or therapy, had 18F-MD-PSMA PET/CT scan within 1 week, and were off hormonal therapy at the time of the scans. The new tracer was compared directly with 11C-choline in sensitivity.

Results: In 3 patients, a side-by-side comparison between 18F-MD-PSMA and 11C-choline was performed, and it was found that the former was about 3 times more sensitive than the latter. The analysis of PET imaging using 18F-MD-PSMA in 191 relapsed patients showed that less than 10% of patients showed the disease limited in the prostate. Among the remote lesions, the number in decreasing order was bone, followed by lymph nodes and other organs. The maximal SUV in lesions in each patient followed an exponential decay, with SUV inclined to the lower end. The Gleason score measured at the diagnosis showed no correlation with the average number of lesions in each patient, the average maximal SUV values among this cohort of patients, and the PSA values measured at the time of PET imaging. The number of lesions observed in each patient has no correlation with the PSA value measured at the time of PET imaging. When PSA value was measured as an independent biomarker at the time of PET imaging, the positivity of PET imaging using 18F-MD-PSMA increased along with an increase in PSA value, but with exceptions where PSMA expression was low or negative. From the PET imaging of this radioligand, the majority of patients showed oligo-metastasis, favoring using local therapy to manage the disease.

Conclusion: An 18F-MD-PSMA as a radioligand was found to be superior to 11C-choline in the setting of patients with biochemical relapse after previous treatment. Its PET imaging results matched those of established PSMA radioligands, but its chemical structure was found to have added features to conjugate with other functional molecules, such as those with therapeutic properties. This radioligand lays the foundation for our further work.

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来源期刊
Current radiopharmaceuticals
Current radiopharmaceuticals PHARMACOLOGY & PHARMACY-
CiteScore
3.20
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4.30%
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43
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