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随着时间的推移,肿瘤与背景的比值显著增加,使得[Zr]Zr-PSMA-617 PET/CT 能够在前列腺癌早期生化复发时定位肿瘤。

Outstanding increase in tumor-to-background ratio over time allows tumor localization by [Zr]Zr-PSMA-617 PET/CT in early biochemical recurrence of prostate cancer.

机构信息

Departments of Nuclear Medicine, Saarland University - Medical Center, Kirrberger Str. 100, Geb. 50, D-66421, Homburg, Germany.

Saarland University, USAAR, Saarbrücken, Germany.

出版信息

Cancer Imaging. 2024 Oct 7;24(1):132. doi: 10.1186/s40644-024-00778-5.

DOI:10.1186/s40644-024-00778-5
PMID:39375762
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11457487/
Abstract

BACKGROUND

Positron emission tomography/computed tomography (PET/CT) using prostate-specific membrane antigen (PSMA)-targeted radiotracers labeled with zirconium-89 (Zr; half-life ~ 78.41 h) showed promise in localizing biochemical recurrence of prostate cancer (BCR) in pilot studies.

METHODS

Retrospective analysis of 38 consecutive men with BCR (median [minimum-maximum] prostate-specific antigen 0.52 (0.12-2.50 ng/mL) undergoing [Zr]Zr-PSMA-617 PET/CT post-negative [Ga]Ga-PSMA-11 PET/CT. PET/CT acquisition 1-h, 24-h, and 48-h post-injection of a median (minimum-maximum) [Zr]Zr-PSMA-617 tracer activity of 123 (84-166) MBq.

RESULTS

[Zr]Zr-PSMA-617 PET/CT detected altogether 57 lesions: 18 local recurrences, 33 lymph node metastases, 6 bone metastases in 30/38 men with BCR (78%) and prior negative conventional PSMA PET/CT. Lesion uptake significantly increased from 1-h to 24-h and, in a majority of cases, from 24-h to 48-h. Tumor-to-background ratios significantly increased over time, with absolute increases of 100 or more. No side effects were noted. After [Zr]Zr-PSMA-617 PET/CT-based treatment, prostate-specific antigen concentration decreased in all patients, becoming undetectable in a third of patients.

LIMITATIONS

retrospective, single center design; infrequent histopathological and imaging verification.

CONCLUSION

This large series provides further evidence that [Zr]Zr-PSMA-617 PET/CT is a beneficial imaging modality to localize early BCR. A remarkable increase in tumor-to-background ratio over time allows localization of tumor unidentified on conventional PSMA PET/CT.

摘要

背景

使用前列腺特异性膜抗原(PSMA)靶向放射性示踪剂标记锝-89(Zr;半衰期~78.41 h)的正电子发射断层扫描/计算机断层扫描(PET/CT)在前列腺癌(PCa)生化复发(BCR)的初步研究中显示出一定的前景。

方法

回顾性分析了 38 例 BCR 患者(中位[最小-最大]前列腺特异性抗原 0.52(0.12-2.50 ng/mL))的连续数据,这些患者在[Ga]Ga-PSMA-11 PET/CT 检查为阴性后行[Zr]Zr-PSMA-617 PET/CT。在注射中位(最小-最大)[Zr]Zr-PSMA-617 示踪剂活性 123(84-166)MBq 后 1、24 和 48 h 进行 PET/CT 采集。

结果

在 38 例有 BCR 的患者中,[Zr]Zr-PSMA-617 PET/CT 共检测到 57 处病灶:18 处局部复发,33 处淋巴结转移,6 处骨骼转移,20 例患者(78%)和之前的常规 PSMA PET/CT 检查为阴性。病灶摄取从 1 h 到 24 h 显著增加,且在大多数情况下,从 24 h 到 48 h 增加。肿瘤与背景的比值随时间显著增加,绝对值增加 100 或更多。未观察到任何副作用。基于[Zr]Zr-PSMA-617 PET/CT 的治疗后,所有患者的前列腺特异性抗原浓度下降,三分之一的患者降至不可检测水平。

局限性

回顾性,单中心设计;组织病理学和影像学验证频率较低。

结论

该大型系列进一步证明[Zr]Zr-PSMA-617 PET/CT 是一种有益的成像方式,可定位早期 BCR。随着时间的推移,肿瘤与背景的比值显著增加,从而可以定位在常规 PSMA PET/CT 上无法识别的肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4588/11457487/e2eb0910fd71/40644_2024_778_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4588/11457487/8369543fd11d/40644_2024_778_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4588/11457487/d889a27158a4/40644_2024_778_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4588/11457487/be90a7ee1a73/40644_2024_778_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4588/11457487/d01593af2dfc/40644_2024_778_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4588/11457487/6553df64a443/40644_2024_778_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4588/11457487/e2eb0910fd71/40644_2024_778_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4588/11457487/8369543fd11d/40644_2024_778_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4588/11457487/d889a27158a4/40644_2024_778_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4588/11457487/be90a7ee1a73/40644_2024_778_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4588/11457487/d01593af2dfc/40644_2024_778_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4588/11457487/6553df64a443/40644_2024_778_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4588/11457487/e2eb0910fd71/40644_2024_778_Fig6_HTML.jpg

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