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Predicting Breast Cancer Chemotherapeutic Response Using a Novel Tool for Microarray Data Analysis

机译:使用新型工具预测乳腺癌化学治疗响应,用于微阵列数据分析

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We developed a novel tool for microarray data analysis that can parsimoniously discover highly predictive genes by finding the optimal trade off between fold change and t-test p value through rigorous cross validation, hi addition to find a small set of highly predictive genes, the tool also has a procedure that recursively discovers and removes predictive genes from the dataset until no such genes can be found. We applied our tool to a public breast cancer dataset with the goal to discover genes that can predict patient's response to a preoperative chemotherapy. The results show that estrogen receptor (ER) gene is the most important gene to predict chemotherapeutic response and no gene signatures can add much clinical benefit for the whole patient population. We further identified a clinically homogenous subgroup of patients (ERnegative, PR-negative and HER2-negative) whose response to the chemotherapy can be reasonably predicted. Many of the discovered predictive markers for this subgroup of patients were successfully validated using a blinded validation set.
机译:我们开发了一种微阵列数据分析的新工具,可以通过严格的交叉验证在折叠变化和T-TEST P值之间找到最佳折衷,为找到一小组高度预测基因,该工具来解开高度预测基因。还具有递归地发现并从数据集中去除预测基因的过程,直到不能发现这些基因。我们将工具应用于公共乳腺癌数据集,目标是发现可以预测患者对术前化疗的反应的基因。结果表明,雌激素受体(ER)基因是预测化学治疗反应的最重要基因,并且没有基因签名可以为整个患者人群增加一些临床效益。我们进一步鉴定了患者的临床同质均质亚组(ORNEGIVE,PR-DIGAL和HER2-DIAL),其对化疗的反应可以合理预测。使用盲的验证集成功验证了该患者亚组的许多发现的预测标记。

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