预测前列腺癌病理分期的创新工具

G. Martorana, A. Bertaccini, S. Viaggi, R. Belleli
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引用次数: 0

摘要

目的:开发一种实用的预测前列腺癌病理分期的工具。材料和方法:从意大利一项前列腺癌纵向观察研究中选择了250例根治性前列腺切除术患者。入选标准如下:术前前列腺特异性抗原(PSA)值<50 ng/ml;临床分期小于或等于T3c期(TNM 1992);活体格里森评分的可用性;在根治性前列腺切除术中获得的病理标本的可用性。病理分期根据病情的加重程度分为五个阶段。对多态有序反应进行多变量logistic回归,以获得疾病进展的预测模型。然后构建了一组平行刻度图,将预测模型转换为一种称为“urogramma”的新工具,该工具能够简化传统图的实际使用。结果:Gleason评分是影响病理分期进展概率最大的因素;PSA和临床分期分别是第二和第三重要因素。双向和三方的相互作用进行了测试,并没有发现显著。年龄和新辅助激素治疗的混杂效应也被测试,它们对反应变量没有显著影响。然后使用逻辑回归算法生成一组nomographs (urogramma),用于使用Gleason评分、PSA水平和疾病的临床分期来预测不同的病理分期。结论:意大利研究获得的预测模型将有助于医生和患者的治疗决策。相对于以往的形态图和多维表,urogramma为病理分期预测提供了一种新的、更简单的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Innovative Tool for Predicting the Pathologic Stage of Prostate Cancer
Objective: To develop a practical tool for predicting the pathologic stage in prostate cancer. Materials and Methods: Two hundred fifty patients who had had radical prostatectomy were selected from an Italian longitudinal observational study on prostate cancer. Inclusion criteria for selection were the following: a preoperative prostate specific antigen (PSA) value <50 ng/ml; a clinical stage less than or equal to stage T3c (TNM 1992); the availability of the bioptic Gleason score; and the availability of a pathologic specimen obtained during the radical prostatectomy. Pathologic stages were categorized into five levels according to the increasing severity of the illness. Multivariate logistic regression on polythomous ordinal response was performed to obtain a predictive model of disease progression. A set of parallel scale nomographs then was constructed to transfer the predictive model into a new tool, called the “Uro-gramma,” that is able to simplify the practical use of the traditional nomograms. Results: The Gleason score was the factor that influenced the probability of pathologic stage progression the most; PSA and clinical stage were the second and third most significant factors, respectively. Two-way and three-way interactions were tested and were not found to be significant. The confounding effects of age and neoadjuvant hormonal therapy also were tested, and they had no significant influence on the response variable. A logistic regression algorithm then was used to produce a set of nomographs (the Uro-gramma) for the prediction of different pathologic stages using the Gleason score, PSA level, and clinical stage of disease. Conclusion: The predictive model obtained from this Italian study will help physicians and patients in therapeutic decision making. The Uro-gramma provides a new and easier instrument with respect to previous nomograms and multidimensional tables for pathologic stage prediction.
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