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基于网络的基因表达检测的设计与多系列验证,用于预测乳腺癌复发和患者生存。

Design and multiseries validation of a web-based gene expression assay for predicting breast cancer recurrence and patient survival.

机构信息

ChipDX LLC, New York, NY 10128, USA.

出版信息

J Mol Diagn. 2011 May;13(3):297-304. doi: 10.1016/j.jmoldx.2010.12.003. Epub 2011 Mar 31.

Abstract

Gene expression analysis is a valuable tool for determining the risk of disease recurrence and overall survival of an individual patient with breast cancer. The purpose of this study was to create and validate a robust prognostic algorithm and implement it within an online analysis environment. Genomic and clinical data from 477 clinically diverse patients with breast cancer were analyzed with Cox regression models to identify genes associated with outcome, independent of standard prognostic factors. Percentile-ranked expression data were used to train a "metagene" algorithm to stratify patients as having a high or low risk of recurrence. The classifier was applied to 1016 patients from five independent series. The 200-gene algorithm stratifies patients into risk groups with statistically and clinically significant differences in recurrence-free and overall survival. Multivariate analysis revealed the classifier to be the strongest predictor of outcome in each validation series. In untreated node-negative patients, 88% sensitivity and 44% specificity for 10-year recurrence-free survival was observed, with positive and negative predictive values of 32% and 92%, respectively. High-risk patients appear to significantly benefit from systemic adjuvant therapy. A 200-gene prognosis signature has been developed and validated using genomic and clinical data representing a range of breast cancer clinicopathological subtypes. It is a strong independent predictor of patient outcome and is available for research use.

摘要

基因表达分析是一种有价值的工具,可以确定乳腺癌患者疾病复发和总体生存的风险。本研究的目的是创建和验证一种稳健的预后算法,并在在线分析环境中实施。对 477 名具有临床多样性的乳腺癌患者的基因组和临床数据进行了 Cox 回归模型分析,以确定与标准预后因素无关的与结局相关的基因。使用百分位排序的表达数据来训练“元基因”算法,将患者分层为高复发风险或低复发风险。该分类器应用于五个独立系列的 1016 名患者。200 个基因算法将患者分层为具有统计学和临床意义的无复发生存率和总体生存率差异的风险组。多变量分析显示,在每个验证系列中,分类器都是最强的预后预测因素。在未经治疗的淋巴结阴性患者中,观察到 10 年无复发生存率的敏感性为 88%,特异性为 44%,阳性预测值为 32%,阴性预测值为 92%。高危患者似乎明显受益于全身辅助治疗。使用代表各种乳腺癌临床病理亚型的基因组和临床数据开发和验证了 200 个基因预后特征。它是患者预后的强有力独立预测因子,可用于研究。

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