Biomarker studies: a call for a comprehensive biomarker study registry

被引:89
作者
Andre, Fabrice [1 ,2 ]
McShane, Lisa M. [3 ]
Michiels, Stefan [4 ]
Ransohoff, David F. [9 ,10 ]
Altman, Douglas G. [8 ]
Reis-Filho, Jorge S. [7 ]
Hayes, Daniel F. [6 ]
Pusztai, Lajos [5 ]
机构
[1] Inst Gustave Roussy, Dept Med Oncol, F-94805 Villejuif, France
[2] Inst Gustave Roussy, INSERM, U981, F-94805 Villejuif, France
[3] US Natl Canc Inst, Biometr Res Branch, DCTD, Bethesda, MD 20892 USA
[4] Inst Jules Bordet, Breast Canc Translat Res Lab, B-1000 Brussels, Belgium
[5] Univ Texas MD Anderson Canc Ctr, Dept Breast Med Oncol, Houston, TX 77230 USA
[6] Univ Michigan, Ctr Comprehens Canc, Ann Arbor, MI 48109 USA
[7] Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
[8] Univ Oxford, Wolfson Coll, Ctr Stat Med, Oxford OX2 6UD, England
[9] Univ N Carolina, Dept Med, Chapel Hill, NC 27599 USA
[10] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27599 USA
关键词
TRIAL REGISTRATION; EXPRESSION; EFFICACY; CHEMOTHERAPY;
D O I
10.1038/nrclinonc.2011.4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor biomarker studies may generate insights into the biological characteristics that drive the clinical behavior of a cancer. Publication bias and hidden multiple hypotheses testing distort the assessment of the true value of biomarkers. Publication bias from preferential reporting of 'positive' findings is well recognized. Hidden multihypothesis testing arises from several biomarkers being tested by different teams using the same samples. The more hypotheses (that is, biomarker association with outcome) tested, the greater the risk of false-positive findings. These biases inflate the potential clinical validity and utility of published biomarkers while negative results often remain hidden. Trial registries have been developed where all phase II and phase III trials should be listed regardless of study outcome. However, such steps have not been taken to reduce such bias in tumor biomarker research. We propose that a registry should be created for biomarker studies initially focused on studies that use specimens from randomized trials. Further development could include nonrandomized studies and deposition of raw data similar to existing genomic data repositories. The benefits of a comprehensive biomarker study registry include more balanced evaluation of proposed markers, fewer false positive leads in research, and hopefully more rapid identification of promising candidate biomarkers.
引用
收藏
页码:171 / 176
页数:6
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