放射组学和放射基因组学目前在预测膀胱癌肿瘤预后中的作用

N. O’Sullivan, Hugo C. Temperley, Alison Corr, J. F. Meaney, Peter E. Lonergan, Michael E Kelly
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引用次数: 0

摘要

放射组学是指将医学影像转化为高通量、可量化的数据,用于分析疾病模式、辅助决策和预测预后。放射基因组学是放射组学的延伸,涉及传统放射组学技术与基因组和转录组数据形式的分子分析的结合。在膀胱癌领域,有研究调查了放射组学和放射基因组学提名图在预测肿瘤分级、基因表达和肿瘤预后方面的开发、实施和效果,结果各不相同。我们的目的是对现有文献进行系统性回顾,调查基于放射组学的提名图的开发情况,以预测膀胱癌的肿瘤预后。 我们对 Medline、EMBASE 和 Web of Science 数据库进行了检索,截止日期为 2023 年 2 月 17 日。此外,还检索了灰色文献,以进一步确定其他合适的出版物。采用诊断准确性研究质量评估2和放射组学质量评分对纳入的研究进行了质量评估。 在所有纳入的研究中,放射基因组提名图在预测主要结果方面普遍表现良好。纳入研究的曲线下面积、灵敏度和特异性的中位数在训练集中分别为 0.83(0.63-0.973)、0.813 和 0.815,在验证集中分别为 0.75(0.702-0.838)、0.723 和 0.652。 多项研究证明了放射组学和放射基因组学模型在晚期盆腔肿瘤学中的预测潜力。为了进一步验证结果并在现代医学中推广应用,还需要在前瞻性环境中开展更大规模的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current role of radiomics and radiogenomics in predicting oncological outcomes in bladder cancer
Radiomics refers to the conversion of medical images into high-throughput, quantifiable data to analyze disease patterns, aid decision-making, and predict prognosis. Radiogenomics is an extension of radiomics and involves a combination of conventional radiomics techniques with molecular analysis in the form of genomic and transcriptomic data. In the field of bladder cancer, studies have investigated the development, implementation, and efficacy of radiomic and radiogenomic nomograms in predicting tumor grade, gene expression, and oncological outcomes, with variable results. We aimed to perform a systematic review of the current literature to investigate the development of a radiomics-based nomogram to predict oncological outcomes in bladder cancer. The Medline, EMBASE, and Web of Science databases were searched up to February 17, 2023. Gray literature was also searched to further identify other suitable publications. Quality assessment of the included studies was performed using the Quality Assessment of Diagnostic Accuracy Studies 2 and Radiomics Quality Score. Radiogenomic nomograms generally had good performance in predicting the primary outcome across the included studies. The median area under the curve, sensitivity, and specificity across the included studies were 0.83 (0.63–0.973), 0.813, and 0.815, respectively, in the training set and 0.75 (0.702–0.838), 0.723, and 0.652, respectively, in the validation set. Several studies have demonstrated the predictive potential of radiomic and radiogenomic models in advanced pelvic oncology. Further large-scale studies in a prospective setting are required to further validate results and allow generalized use in modern medicine.
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