Pathologic outcome of incidentally detected tracer-avid lesions in 68Ga-PSMA-11 PET/CT for prostate cancer.

Radiology advances Pub Date : 2024-04-30 eCollection Date: 2024-05-01 DOI:10.1093/radadv/umae008
Darryl Mar, Devan Diwanji, Blair Lowery, Li Zhang, Thomas A Hope, Spencer C Behr, Robert R Flavell
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Abstract

Background: Prostate-specific membrane antigen (PSMA) PET is effective in identifying prostate cancer metastases. However, PSMA PET uptake has also been described in other lesions, including nonprostate malignancies and benign processes.

Purpose: To identify causes of unexpected radiopharmaceutical accumulation on PSMA PET.

Materials and methods: A total of 2,054 study reports representing 1,873 unique patients who had undergone 68Ga-PSMA-11 PET/CT scans at a single large academic center from December 2015 to April 2022 were retrospectively reviewed for the mention of unexpected PSMA uptake not initially thought to represent metastatic prostate cancer. Scans with pathologic outcome were reviewed by 2 blinded readers for scan indication and lesion location and quantitative parameters.

Results: In 48 patients, the PSMA ligand-avid incidental lesions revealed 19 cases of second malignancies, 17 cases of prostate cancer, and 13 cases of benign lesions. The most common lesion locations were lung (14), thyroid (14), lymph nodes (8), and bowel (4). Benign lesions exhibited lower molecular imaging PSMA scores (median: 1; interquartile range [IQR]: 1.00-1.25; P = .017) than metastatic prostate lesions (median: 2; IQR: 1-3). Second malignancies were larger (median: 34 mm; IQR: 27-39 mm) than metastatic prostate cancer (median: 14 mm; IQR: 12-19 mm; P = .001) and benign lesions (median: 19 mm; IQR: 13.00-31.00 mm; P = .03). PSMA ligand-avid lesions in scans performed in the initial staging for prostate cancer were more commonly associated with a diagnosis of a secondary malignancy than with metastatic prostate cancer (0 vs 8 lesions, P = .008). Higher standardized uptake value maximum was observed for metastatic prostate cancer and second malignancy when compared with benign outcome.

Conclusion: Features that influence the probability of an incidental lesion representing a malignancy include lesion location, reason for the PSMA PET/CT study, and associated imaging features (size, standardized uptake value maximum, and molecular imaging PSMA score).

68Ga-PSMA-11 PET/CT偶然发现的前列腺癌示踪病灶的病理结果
背景:前列腺特异性膜抗原(PSMA) PET是鉴别前列腺癌转移的有效方法。然而,PSMA PET摄取也被描述为其他病变,包括非前列腺恶性肿瘤和良性病变。目的:确定PSMA PET上意外放射性药物积聚的原因。材料和方法:回顾性回顾了2015年12月至2022年4月在单个大型学术中心接受68Ga-PSMA-11 PET/CT扫描的1873名独特患者的2054项研究报告,以提及最初未被认为是转移性前列腺癌的意外PSMA摄取。2位盲法读者回顾扫描的病理结果,以确定扫描指征、病变位置和定量参数。结果:48例患者PSMA配体附带病变中发现第二恶性肿瘤19例,前列腺癌17例,良性病变13例。最常见的病变部位为肺(14例)、甲状腺(14例)、淋巴结(8例)和肠(4例)。良性病变分子影像学PSMA评分较低(中位数:1;四分位间距[IQR]: 1.00-1.25; P =。017)比转移性前列腺病变(中位数:2;IQR: 1-3)。第二恶性肿瘤(中位数:34 mm; IQR: 27-39 mm)大于转移性前列腺癌(中位数:14 mm; IQR: 12-19 mm; P =。001)和良性病变(中位数:19 mm; IQR: 13.00-31.00 mm; P = .03)。在前列腺癌的初始阶段扫描中,PSMA配体病变更常与继发性恶性肿瘤的诊断相关,而不是与转移性前列腺癌的诊断相关(0 vs 8个病变,P = 0.008)。与良性结果相比,转移性前列腺癌和第二恶性肿瘤的标准化摄取值最大值更高。结论:影响偶发性病变代表恶性肿瘤可能性的特征包括病变位置、PSMA PET/CT检查的原因以及相关的影像学特征(大小、标准化摄取值最大值和分子影像学PSMA评分)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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