前列腺特异性膜抗原正电子发射断层扫描/计算机断层扫描在前列腺癌诊断中的辐射组学模型

Cancers Pub Date : 2024-05-16 DOI:10.3390/cancers16101897
L. Huynh, Shea Swanson, Sophia Cima, Eliana Haddadin, Michael Baine
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引用次数: 0

摘要

前列腺膜特异性抗原(PSMA)正电子发射断层扫描和计算机断层扫描(PET/CT)扫描的临床整合为前列腺癌(PC)预后的高级数据分析技术提供了潜力。在这些工具中,放射组学是一种基于计算机的方法,用于提取和定量分析医学成像中的次视觉特征。在此背景下,本综述旨在总结目前有关 PSMA PET/CT 衍生放射组学用于 PC 风险分层的文献。我们对2017年至2023年发表的文献进行了逐步检索。在23篇关于PSMA PET/CT衍生前列腺放射组学的文章中,PC诊断、活检格雷森评分(GS)预测、不良病理预测和治疗结果分别是4篇(17.4%)、5篇(21.7%)、7篇(30.4%)和7篇(30.4%)研究的主要终点。在预测 PC 诊断方面,PSMA PET/CT 衍生模型表现良好,接收器操作特征曲线下面积(ROC-AUC)值为 0.85-0.925。同样,在活检和手术病理结果预测方面,ROC-AUC 值范围分别为 0.719-0.84 和 0.84-0.95。最后,9 项研究探讨了治疗后的复发、进展或生存预测,其 ROC-AUC 值范围为 0.698-0.90。在纳入本综述的 23 项研究中,有 2 项研究(8.7%)进行了外部验证。虽然对 PSMA PET/CT 衍生放射模型的探索在随访和经验方面尚不成熟,但这些结果代表了未来调查和探索的巨大潜力。不过,在考虑用于临床之前,必须优先对放射组特征的特征重现性和生物学验证进行严格验证。
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Prostate-Specific Membrane Antigen Positron Emission Tomography/Computed Tomography-Derived Radiomic Models in Prostate Cancer Prognostication
The clinical integration of prostate membrane specific antigen (PSMA) positron emission tomography and computed tomography (PET/CT) scans represents potential for advanced data analysis techniques in prostate cancer (PC) prognostication. Among these tools is the use of radiomics, a computer-based method of extracting and quantitatively analyzing subvisual features in medical imaging. Within this context, the present review seeks to summarize the current literature on the use of PSMA PET/CT-derived radiomics in PC risk stratification. A stepwise literature search of publications from 2017 to 2023 was performed. Of 23 articles on PSMA PET/CT-derived prostate radiomics, PC diagnosis, prediction of biopsy Gleason score (GS), prediction of adverse pathology, and treatment outcomes were the primary endpoints of 4 (17.4%), 5 (21.7%), 7 (30.4%), and 7 (30.4%) studies, respectively. In predicting PC diagnosis, PSMA PET/CT-derived models performed well, with receiver operator characteristic curve area under the curve (ROC-AUC) values of 0.85–0.925. Similarly, in the prediction of biopsy and surgical pathology results, ROC-AUC values had ranges of 0.719–0.84 and 0.84–0.95, respectively. Finally, prediction of recurrence, progression, or survival following treatment was explored in nine studies, with ROC-AUC ranging 0.698–0.90. Of the 23 studies included in this review, 2 (8.7%) included external validation. While explorations of PSMA PET/CT-derived radiomic models are immature in follow-up and experience, these results represent great potential for future investigation and exploration. Prior to consideration for clinical use, however, rigorous validation in feature reproducibility and biologic validation of radiomic signatures must be prioritized.
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