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新型探针[123I]I-PSMA-7 在人源体内的首次临床前评估,用于前列腺癌实时术中靶向活检和 SPECT/CT 成像。

The first-in-human preclinical evaluation of the new probe [123I]I-PSMA-7 for real-time intraoperative targeted biopsy and SPECT/CT imaging in prostate cancer.

机构信息

Department of Nuclear Medicine, The First Medical Centre of Chinese PLA General Hospital, Beijing, China.

Chinese PLA General Hospital, Chinese PLA Medical School, Beijing, China.

出版信息

Eur J Nucl Med Mol Imaging. 2024 Nov;51(13):4141-4150. doi: 10.1007/s00259-024-06833-4. Epub 2024 Jul 23.

Abstract

PURPOSE

PSMA/PET has been increasingly used to detect PCa, and PSMA/PET-guided biopsy has shown promising results. However, it cannot be confirmed immediately whether the tissues are the targeted area. In this study, we aimed to develop a novel probe, [I]I-PSMA-7. First, we hope that [I]I-PSMA-7 can provide instant confirmation for prostate biopsy. Second, we hope it will help detect PCa.

METHODS

We synthesized a high-affinity probe, [I]I-PSMA-7, and evaluated its properties. We included ten patients with suspected PCa and divided them into two groups. The injection and biopsy were approximately 24 h apart. The activity in biopsy lesions was measured as the cpm by a γ-counter. Moreover, we enrolled 3 patients to evaluate the potential of [I]I-PSMA-7 for detecting PCa.

RESULTS

Animal experiments verified the safety, targeting and effectiveness of [I]I-PSMA-7, and the tumor-to-muscle ratio was greatest at 24 h, which confirmed the results of this study in humans. After injection of 185MBq [I]I-PSMA-7, 18/55 cores were positive, and the cpm was significantly greater (4345 ± 3547 vs. 714 ± 547, P < 0.001), with an AUC of 0.97 and a cutoff of 1312 (sens/spec of 94.40%/91.90%). At a lower dose, 10/55 biopsy cores were cancerous, and the cpm was 2446 ± 1622 vs. 153 ± 112 (P < 0.001). The AUC was 1, with a cutoff value of 490 (sens/spec of 100%). When the radiopharmaceuticals were added to 370 MBq, we achieved better SPECT/CT imaging.

CONCLUSION

With the aid of [I]I-PSMA-7 and via cpm-based biopsy, we can reduce the number of biopsies to a minimum operation. [I]I-PSMA-7 PSMA SPECT/CT can also provide good imaging results.

TRIAL REGISTRATION

Chinese Clinical trial registry ChiCTR2300069745, Registered 24 March 2023.

摘要

目的

PSMA/PET 已越来越多地用于检测前列腺癌,PSMA/PET 引导的活检显示出了良好的效果。然而,目前还无法立即确认组织是否为靶向区域。在本研究中,我们旨在开发一种新型探针,即[I]I-PSMA-7。首先,我们希望[I]I-PSMA-7 能够为前列腺活检提供即时确认。其次,我们希望它能够帮助检测前列腺癌。

方法

我们合成了一种高亲和力的探针[I]I-PSMA-7,并对其性质进行了评估。我们纳入了 10 名疑似患有前列腺癌的患者,并将其分为两组。注射和活检大约相隔 24 小时。γ计数器测量活检病变中的活性,以 cpm 表示。此外,我们还招募了 3 名患者,以评估[I]I-PSMA-7 检测前列腺癌的潜力。

结果

动物实验验证了[I]I-PSMA-7 的安全性、靶向性和有效性,24 小时时肿瘤与肌肉的比值最大,这与人类研究结果一致。注射 185MBq[I]I-PSMA-7 后,18/55 个核心呈阳性,cpm 显著更高(4345 ± 3547 比 714 ± 547,P<0.001),AUC 为 0.97,截断值为 1312(94.40%/91.90%的敏感度/特异性)。在较低剂量下,10/55 个活检核心呈癌性,cpm 为 2446 ± 1622 比 153 ± 112(P<0.001)。AUC 为 1,截断值为 490(100%的敏感度/特异性)。当放射性药物增加到 370MBq 时,我们实现了更好的 SPECT/CT 成像。

结论

借助[I]I-PSMA-7 和基于 cpm 的活检,我们可以将活检次数减少到最低限度。[I]I-PSMA-7 PSMA SPECT/CT 还可以提供良好的成像结果。

试验注册

中国临床试验注册中心 ChiCTR2300069745,注册于 2023 年 3 月 24 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2f7/11527917/44795de69728/259_2024_6833_Fig1_HTML.jpg

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