Prognostic and predictive signatures for treatment decisions

被引:0
|
作者
Lee, Un Jung [1 ]
Tzeng, ShengLi [2 ]
Chen, Yu-Chuan [3 ]
Chen, James J. [4 ]
机构
[1] US FDA, Div Biochem Toxicol, Natl Ctr Toxicol Res, 3900 NCTR Rd, Jefferson, AR 72079 USA
[2] Acad Sinica, Inst Stat Sci, 128 Acad Rd,Sect 2, Taipei 11529, Taiwan
[3] US FDA, Div Bioinformat & Biostat, Natl Ctr Toxicol Res, 3900 NCTR Rd, Jefferson, AR 72029 USA
[4] Univ Arkansas Med Sci, Dept Stat, Little Rock, AR 72205 USA
关键词
biomarker identification; clinical trial; interaction test; predictive classifiers; subgroup selection; tailored therapy; SUBGROUP IDENTIFICATION; BIOMARKER CLASSIFIERS; CLINICAL-TRIALS; CANCER; CLASSIFICATION; CHALLENGES; COMPONENTS; REGRESSION; SELECTION; DESIGN;
D O I
10.2217/bmm-2017-0320
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aim: We develop a subgroup selection procedure using both prognostic and predictive biomarkers to identify four patient subpopulations: low-and high-risk responders, and low-and high-risk nonresponders. Methods: We utilize three regression models to identify three sets of biomarkers: S, prognostic biomarkers; T, predictive biomarkers; and U, prognostic and predictive biomarkers. The prognostic signature C(S) combines with a predictive signature, either C(T) or C(U), to develop two procedures C(S, T) and C(S, U) for identification of four subgroups. Results: Simulation experiment showed that proposed models for identifying the biomarker sets S and U performed well, as did the procedure C(S, U) for subgroup identification. Conclusion: The proposed model provides more comprehensive characterization of patient subpopulations, and better accuracy in patient treatment assignment.
引用
收藏
页码:849 / 859
页数:11
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