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包含核基质蛋白22的列线图用于预测Ta、T1期或原位癌膀胱移行细胞癌患者的疾病复发和进展。

Nomograms including nuclear matrix protein 22 for prediction of disease recurrence and progression in patients with Ta, T1 or CIS transitional cell carcinoma of the bladder.

作者信息

Shariat Shahrokh F, Zippe Craig, Lüdecke Gerson, Boman Hans, Sanchez-Carbayo Marta, Casella Roberto, Mian Christine, Friedrich Martin G, Eissa Sanaa, Akaza Hideyuki, Sawczuk Ihor, Serretta Vincenzo, Huland Hartwig, Hedelin Hans, Rupesh Raina, Miyanaga Naoto, Sagalowsky Arthur I, Wians Frank, Roehrborn Claus G, Lotan Yair, Perrotte Paul, Benayoun Serge, Marberger Michael J, Karakiewicz Pierre I

机构信息

Department of Urology, The University of Texas Southwestern Medical Center, Dallas, Texas 75390-9110, USA.

出版信息

J Urol. 2005 May;173(5):1518-25. doi: 10.1097/01.ju.0000154696.48217.75.

Abstract

PURPOSE

We developed and validated nomograms that accurately predict disease recurrence and progression in patients with Ta, T1, or CIS transitional cell carcinoma (TCC) of the bladder using a large international cohort.

METHODS

Univariate and multivariate logistic regression models targeted histologically confirmed disease recurrence, and focused on 2,542 patients with bladder TCC from 10 participating centers. Variables consisted of pre-cystoscopy voided urine Nuclear Matrix Protein 22 (NMP22) assay, urine cytology, age and gender. Resulting nomograms were internally validated with bootstrapping. Nomogram performance was explored graphically with Loess smoothing plots.

RESULTS

Overall 957 patients had recurrent TCC. Tumor grade and stage was available for 898 patients, including 24% grade I, 43% grade II, and 33% grade III; 45% stage Ta, 32% T1 and/or CIS, and 23% T2 or greater. Bootstrap corrected predictive accuracy for any TCC recurrence was 0.842; grade III Ta/T1 or CIS was 0.869; and T2 or higher stage TCC of any grade was 0.858. Virtually perfect performance characteristics were observed for the nomograms predicting any TCC recurrence or grade III Ta/T1 or CIS. The nomogram predicting T2 or higher stage TCC overestimated the observed probability for predicted values greater than 45%.

CONCLUSIONS

We developed and internally validated nomograms that incorporate urinary NMP22, cytology, age and gender to predict with high accuracy the probability of disease recurrence and progression in patients with Ta, T1, and/or CIS bladder TCC. These nomograms could provide a means for individualizing followup in patients with Ta, T1, CIS bladder TCC.

摘要

目的

我们使用一个大型国际队列开发并验证了能准确预测膀胱Ta、T1或CIS期移行细胞癌(TCC)患者疾病复发和进展的列线图。

方法

单因素和多因素逻辑回归模型针对经组织学证实的疾病复发,纳入了来自10个参与中心的2542例膀胱TCC患者。变量包括膀胱镜检查前的排尿后尿液核基质蛋白22(NMP22)检测、尿液细胞学检查、年龄和性别。所得列线图通过自抽样法进行内部验证。使用局部加权回归(Loess)平滑图以图形方式探究列线图的性能。

结果

共有957例患者出现TCC复发。898例患者有肿瘤分级和分期信息,其中24%为I级,43%为II级,33%为III级;45%为Ta期,32%为T1期和/或CIS期,23%为T2期或更高分期。任何TCC复发的自抽样法校正预测准确率为0.842;III级Ta/T1或CIS期为0.869;任何分级的T2期或更高分期TCC为0.858。在预测任何TCC复发或III级Ta/T1或CIS期的列线图中观察到了几乎完美的性能特征。预测T2期或更高分期TCC的列线图对于预测值大于45%的情况高估了观察到的概率。

结论

我们开发并内部验证了结合尿液NMP22、细胞学检查、年龄和性别的列线图,以高精度预测Ta、T1和/或CIS期膀胱TCC患者疾病复发和进展的概率。这些列线图可为Ta、T1、CIS期膀胱TCC患者的个体化随访提供一种方法。

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