临床局限性前列腺癌治疗的生化复发和生存预测模型

Ashutosh Tewari , Eduard J. Gamito , E. David Crawford , Mani Menon
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引用次数: 7

摘要

在过去的几年中,出现了许多新的预测建模技术。这些方法已经在人工智能研究、工程和气象学等领域得到了发展,现在正被应用于医学问题,并取得了可喜的成果。这篇综述概述了我们最近的工作,使用了一些先进的技术,如人工神经网络、遗传算法和倾向评分,以开发有用的模型来估计临床上局限性前列腺癌男性的生化复发风险和长期生存。此外,我们还描述了我们为开发一个全面的前列腺癌数据库所做的努力,该数据库与这些新颖的建模技术一起,提供了一个强大的研究工具,可以根据年龄、种族和合并症等因素对治疗失败和生存的风险进行分层。利用1400例患者的临床和病理资料建立生化复发模型。该模型的受试者工作特征曲线下面积为0.83,灵敏度为85%,特异性为74%。对于生存模型,研究人员使用了6149名男性的数据。我们的分析表明,年龄、收入和合并症对生存率有统计学上显著的影响。种族的影响在这方面没有达到统计学意义。模型总生存期C指数值为0.69。我们的结论是,这些方法,以及一个全面的数据库,允许模型的发展,提供治疗失败风险和生存概率的估计,比以前开发的更有意义和临床有用。
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Biochemical Recurrence and Survival Prediction Models for the Management of Clinically Localized Prostate Cancer

A number of new predictive modeling techniques have emerged in the past several years. These methods, which have been developed in fields such as artificial intelligence research, engineering, and meteorology, are now being applied to problems in medicine with promising results. This review outlines our recent work with use of selected advanced techniques such as artificial neural networks, genetic algorithms, and propensity scoring to develop useful models for estimating the risk of biochemical recurrence and long-term survival in men with clinically localized prostate cancer. In addition, we include a description of our efforts to develop a comprehensive prostate cancer database that, along with these novel modeling techniques, provides a powerful research tool that allows for the stratification of risk for treatment failure and survival by such factors as age, race, and comorbidities. Clinical and pathologic data from 1400 patients were used to develop the biochemical recurrence model. The area under the receiver operating characteristic curve for this model was 0.83, with a sensitivity of 85% and specificity of 74%. For the survival model, data from 6149 men were used. Our analysis indicated that age, income, and comorbidities had a statistically significant impact on survival. The effect of race did not reach statistical significance in this regard. The C index value for the model was 0.69 for overall survival. We conclude that these methods, along with a comprehensive database, allow for the development of models that provide estimates of treatment failure risk and survival probability that are more meaningful and clinically useful than those previously developed.

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