A BAYESIAN MODEL OF DOSE-RESPONSE FOR CANCER DRUG STUDIES

被引:3
|
作者
Tansey, Wesley [1 ]
Tosh, Christopher [2 ]
Blei, David M. [2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, 1275 York Ave, New York, NY 10021 USA
[2] Columbia Univ, Data Sci Inst, New York, NY 10027 USA
来源
ANNALS OF APPLIED STATISTICS | 2022年 / 16卷 / 02期
关键词
Dose-response; matrix factorization; trend filtering; slice sampling; constrained inference; NONPARAMETRIC-ESTIMATION; TRASTUZUMAB RESISTANCE; HORSESHOE ESTIMATOR; ISOTONIC REGRESSION; SHRINKAGE;
D O I
10.1214/21-AOAS1485
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
Exploratory cancer drug studies test multiple tumor cell lines against multiple candidate drugs. The goal in each paired (cell line, drug) experiment is to map out the dose-response curve of the cell line as the dose level of the drug increases. We propose Bayesian tensor filtering (BTF), a hierarchical Bayesian model for dose-response modeling in multisample, multitreatment cancer drug studies. BTF uses low-dimensional embeddings to share statistical strength between similar drugs and similar cell lines. Structured shrinkage priors in BTF encourage smoothness in the dose-response curves while remaining adaptive to sharp jumps when the data call for it. We focus on a pair of cancer drug studies exhibiting a particular pathology in their experimental design, leading us to a nonconjugate monotone mixture-of-gammas likelihood. To perform posterior inference, we develop a variant of the elliptical slice sampling algorithm for sampling from linearly-constrained multivariate normal priors with nonconjugate likelihoods. In benchmarks, BTF outperforms state-of-the-art methods for covariance regression and dynamic Poisson matrix factorization. On the two cancer drug studies, BTF outperforms the current standard approach in biology and reveals potential new biomarkers of drug sensitivity in cancer.
引用
收藏
页码:680 / 705
页数:26
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