Laboratory of Functional Genomics, Charité, Charitéplatz 1, 10117 Berlin, Germany.
Breast Cancer Res Treat. 2012 Apr;132(3):1025-34. doi: 10.1007/s10549-011-1676-y. Epub 2011 Jul 16.
In the last decades, several gene expression-based predictors of clinical behavior were developed for breast cancer. A common feature of these is the use of multiple genes to predict hormone receptor status and the probability of tumor recurrence, survival or response to chemotherapy. We developed an online analysis tool to compute ER and HER2 status, Oncotype DX 21-gene recurrence score and an independent recurrence risk classification using gene expression data obtained by interrogation of Affymetrix microarray profiles. We implemented rigorous quality control algorithms to promptly exclude any biases related to sample processing, hybridization and scanning. After uploading the raw microarray data, the system performs the complete evaluation automatically and provides a report summarizing the results. The system is accessible online at http://www.recurrenceonline.com . We validated the system using data from 2,472 publicly available microarrays. The validation of the prediction of the 21-gene recurrence score was significant in lymph node negative patients (Cox-Mantel, P = 5.6E-16, HR = 0.4, CI = 0.32-0.5). A correct classification was obtained for 88.5% of ER- and 90.5% of ER + tumors (n = 1,894). The prediction of recurrence risk in all patients by using the mean of the independent six strongest genes (P < 1E-16, HR = 2.9, CI = 2.5-3.3), of the four strongest genes in lymph node negative ER positive patients (P < 1E-16, HR = 2.8, CI = 2.2-3.5) and of the three genes in lymph node positive patients (P = 3.2E-9, HR = 2.5, CI = 1.8-3.4) was highly significant. In summary, we integrated available knowledge in one platform to validate currently used predictors and to provide a global tool for the online determination of different prognostic parameters simultaneously using genome-wide microarrays.
在过去的几十年中,已经开发出了几种基于基因表达的预测乳腺癌临床行为的方法。这些方法的一个共同特点是使用多个基因来预测激素受体状态和肿瘤复发、生存或对化疗的反应概率。我们开发了一个在线分析工具,用于计算 ER 和 HER2 状态、Oncotype DX 21 基因复发评分以及使用 Affymetrix 微阵列谱分析获得的基因表达数据进行的独立复发风险分类。我们实施了严格的质量控制算法,以迅速排除与样本处理、杂交和扫描相关的任何偏差。上传原始微阵列数据后,系统会自动执行完整评估,并提供总结结果的报告。该系统可在 http://www.recurrenceonline.com 在线访问。我们使用 2472 个公开可用的微阵列数据验证了该系统。在淋巴结阴性患者中,21 基因复发评分预测的验证具有统计学意义(Cox-Mantel,P = 5.6E-16,HR = 0.4,CI = 0.32-0.5)。对于 ER-和 90.5%的 ER+肿瘤(n = 1,894),获得了正确的分类。使用独立的 6 个最强基因的平均值(P < 1E-16,HR = 2.9,CI = 2.5-3.3)、淋巴结阴性 ER 阳性患者中最强的 4 个基因(P < 1E-16,HR = 2.8,CI = 2.2-3.5)和淋巴结阳性患者中的 3 个基因(P = 3.2E-9,HR = 2.5,CI = 1.8-3.4),对所有患者的复发风险进行预测具有高度统计学意义。总之,我们将现有知识集成到一个平台中,以验证目前使用的预测因子,并提供一个使用全基因组微阵列同时在线确定不同预后参数的全局工具。