4.7 Article

Adaptive Prediction Model in Prospective Molecular Signature-Based Clinical Studies

期刊

CLINICAL CANCER RESEARCH
卷 20, 期 3, 页码 531-539

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AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-13-2127

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资金

  1. NIH [5R01CA152301, 1R01CA172211, 4R33DA027592]
  2. University of Texas SPORE in Lung Cancer [P50CA70907]
  3. Cancer Prevention Research Institute of Texas [RP101251]

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Use of molecular profiles and clinical information can help predict which treatment would give the best outcome and survival for each individual patient, and thus guide optimal therapy, which offers great promise treatment plan. The gold standard for evaluating the prediction models is prospective clinical studies, in which patients are enrolled sequentially. However, there is no statistical method using this sequential feature to adapt the prediction model to the current patient cohort. In this article, we propose a reweighted random forest ( RWRF) model, which updates the weight of each decision tree whenever additional patient information is available, to account for the potential heterogeneity between training and testing data. A simulation study and a lung cancer example are used to show that the proposed method can adapt the prediction model to current patients' characteristics, and, therefore, can improve prediction accuracy significantly. We also show that the proposed method can identify important and consistent predictive variables. Compared with rebuilding the prediction model, the RWRF updates a well-tested model gradually, and all of the adaptive procedure/parameters used in the RWRF model are prespecified before patient recruitment, which are important practical advantages for prospective clinical studies. (C) 2013 AACR.

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