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Development and Blind Clinical Validation of a MicroRNA Based Predictor of Response to Treatment with R-CHO(E)P in DLBCL

机译:基于Microrna的响应预测因子的开发和盲临床验证在DLBCL中的r-cho(e)p治疗

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Based on the measured growth inhibition of 60 human cancer cell lines (NCI60) in the presence of doxorubicine, cyclophosphamide, vincristine and etoposide as well as the baseline microRNA expression of the 60 cell lines, a microRNA based response predictor to CHOP was developed. The response predictor consisting of 20 microRNAs was blindly validated in a cohort of 116 de novo DLBCL patients treated with R-CHOP or R-CHOEP as first line treatment. The predicted sensitivity based on diagnostic FFPE samples matched the clinical response, with decreasing sensitivity in poor responders (P=0.03). When the International Prognostic Index (IPI) was included in the prediction analysis, the separation between responders and non-responders improved (P=0.001).
机译:基于测量的60个人癌细胞系(NCI60)在多柔枯胺,环磷酰胺,长春螯合物以及60个细胞系的基线microRNA表达的基础上,开发了一种基于30个细胞系的基线MicroRNA表达。 由20 microRNA组成的反应预测因子在116 de Novo DLBCL患者的群组中盲目地验证了R-Chec或R-Choep作为第一线治疗。 基于诊断FFPE样品的预测敏感性匹配临床反应,降低较差响应者的敏感性(P = 0.03)。 当在预测分析中包含国际预后指数(IPI)时,响应者和非响应者之间的分离改善(P = 0.001)。

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