[68Ga]Ga-PSMA-11 PET and Prostate Cancer Bone Metastases: Diagnostic Performance of Available Standardized Criteria.

Ismini C Mainta, Angeliki Neroladaki, Nicola Bianchetto Wolf, Daniel Benamran, Sana Boudabbous, Thomas Zilli, Valentina Garibotto
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引用次数: 0

Abstract

In up to two thirds of prostate-specific membrane antigen (PSMA) PET scans, unspecific bone uptake has been described. The aim of this study was to estimate the diagnostic accuracy of [68Ga]Ga-PSMA-11 PET/CT for bone metastases and the occurrence of equivocal lesions. Methods: We analyzed retrospectively 118 patients who underwent a [68Ga]Ga-PSMA-11 PET/CT for initial staging or recurrence evaluation. Lesions were interpreted according to the PSMA reporting and data system (PSMA-RADS) and the prostate cancer molecular imaging standardized evaluation (PROMISE) criteria. The SUVmax and the localization of each lesion were recorded. A combination of prior or follow-up examinations was used as a reference standard to categorize benign and malignant lesions. Correlation between the final diagnosis and imaging or clinicobiochemical parameters was tested. The diagnostic accuracy was calculated for different cutoffs of PSMA-RADS criteria, for PROMISE criteria, and the sequential combination of both. Results: In total, 265 bone abnormalities were identified in 70 of 118 patients. Among these, 148 (55.8%) lesions in 50 (42.4%) patients were classified as PSMA-RADS-3B. There were no PSMA-RADS-3D lesions in our cohort. Equivocal lesions were more frequent on the ribs (30.6%) followed by the pelvis (26.5%), but in the ribs, such an uptake was malignant in 33.3% of cases versus 66.7% in the pelvis. A significant association was found between the final diagnosis and the SUVmax, prostate-specific antigen (PSA), PSA doubling time, International Society of Urological Pathology score, and the number of foci. The sensitivity and specificity were 100% and 63.6% for the PSMA-RADS-3B cutoff, respectively; 40.5% and 100% for the PSMA-RADS-4 cutoff, respectively; and 89.3% and 96.6% for both the PROMISE criteria and the sequential PSMA-RADS/PROMISE strategy, respectively. In the sequential method, the number of equivocal lesions was reduced from 147 to 2. We found that 53% of PSMA-RADS-3B lesions were malignant; 95.5% of lesions classified positive by the sequential method were true positives, whereas 32.6% were false negatives. Conclusion: [68Ga]Ga-PSMA-11 PET/CT has high accuracy for the diagnosis of bone metastases. Equivocal lesions constitute nearly half of the lesions seen on PSMA PET. The sequential combination of PSMA-RADS and PROMISE criteria reduces the number of lesions classified as equivocal. PSMA-RADS-3B lesions which are positive according to the PROMISE criteria should be considered highly suggestive of malignancy.

[68Ga]Ga-PSMA-11 PET 与前列腺癌骨转移:现有标准化标准的诊断性能。
据描述,在多达三分之二的前列腺特异性膜抗原(PSMA)PET扫描中,存在非特异性骨摄取。本研究的目的是评估[68Ga]Ga-PSMA-11 PET/CT 对骨转移的诊断准确性,以及等位病变的发生率。方法:我们回顾性分析了118例接受[68Ga]Ga-PSMA-11 PET/CT进行初始分期或复发评估的患者。病灶根据 PSMA 报告和数据系统(PSMA-RADS)和前列腺癌分子成像标准化评估(PROMISE)标准进行解释。记录每个病灶的 SUVmax 和定位。在对良性和恶性病变进行分类时,采用了先前或后续检查的组合作为参考标准。测试了最终诊断与成像或临床生化参数之间的相关性。计算了PSMA-RADS标准、PROMISE标准的不同临界值以及两者的顺序组合的诊断准确性。结果:118 名患者中有 70 名骨质异常。其中,50 名患者(42.4%)的 148 个病灶(55.8%)被归类为 PSMA-RADS-3B。我们的队列中没有 PSMA-RADS-3D 病变。肋骨(30.6%)和骨盆(26.5%)上的等密度病变更为常见,但在肋骨病例中,33.3%的病变摄取为恶性,而在骨盆病例中,66.7%的病变摄取为恶性。最终诊断结果与 SUVmax、前列腺特异性抗原(PSA)、PSA 加倍时间、国际泌尿病理学会评分和病灶数量之间存在明显关联。PSMA-RADS-3B截断值的灵敏度和特异性分别为100%和63.6%;PSMA-RADS-4截断值的灵敏度和特异性分别为40.5%和100%;PROMISE标准和PSMA-RADS/PROMISE序列策略的灵敏度和特异性分别为89.3%和96.6%。我们发现53%的PSMA-RADS-3B病变是恶性的;95.5%被序列法归类为阳性的病变是真阳性,而32.6%是假阴性。结论[68Ga]Ga-PSMA-11 PET/CT 对骨转移瘤的诊断具有很高的准确性。在 PSMA PET 上看到的病灶中,近一半为等信号病灶。PSMA-RADS和PROMISE标准的连续组合可减少被归类为等焦病灶的数量。根据 PROMISE 标准呈阳性的 PSMA-RADS-3B 病变应被视为高度提示恶性肿瘤。
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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