A simple and reproducible breast cancer prognostic test

被引:35
|
作者
Marchionni, Luigi [1 ]
Afsari, Bahman [4 ]
Geman, Donald [3 ,4 ]
Leek, Jeffrey T. [2 ,5 ]
机构
[1] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Inst Computat Med, Baltimore, MD 21218 USA
[4] Johns Hopkins Univ, Dept Appl Math & Stat, Baltimore, MD 21218 USA
[5] Johns Hopkins Univ, Ctr Computat Biol, Baltimore, MD 21205 USA
来源
BMC GENOMICS | 2013年 / 14卷
关键词
Reproducible research; Gene expression analysis; Biomarkers; Top scoring pair; Prediction; Genomics; Personalized medicine; Breast cancer; MammaPrint; 2-GENE CLASSIFIER; SIGNATURE; PREDICTOR; MARKER;
D O I
10.1186/1471-2164-14-336
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: A small number of prognostic and predictive tests based on gene expression are currently offered as reference laboratory tests. In contrast to such success stories, a number of flaws and errors have recently been identified in other genomic-based predictors and the success rate for developing clinically useful genomic signatures is low. These errors have led to widespread concerns about the protocols for conducting and reporting of computational research. As a result, a need has emerged for a template for reproducible development of genomic signatures that incorporates full transparency, data sharing and statistical robustness. Results: Here we present the first fully reproducible analysis of the data used to train and test MammaPrint, an FDA-cleared prognostic test for breast cancer based on a 70-gene expression signature. We provide all the software and documentation necessary for researchers to build and evaluate genomic classifiers based on these data. As an example of the utility of this reproducible research resource, we develop a simple prognostic classifier that uses only 16 genes from the MammaPrint signature and is equally accurate in predicting 5-year disease free survival. Conclusions: Our study provides a prototypic example for reproducible development of computational algorithms for learning prognostic biomarkers in the era of personalized medicine.
引用
收藏
页数:7
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