A Pan-Cancer and Polygenic Bayesian Hierarchical Model for the Effect of Somatic Mutations on Survival

We built a novel Bayesian hierarchical survival model based on the somatic mutation profile of patients across 50 genes and 27 cancer types. The pan-cancer quality allows for the model to “borrow” information across cancer types, motivated by the assumption that similar mutation profiles may have si...

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Main Authors: Sarah Samorodnitsky, Katherine A Hoadley, Eric F Lock
Format: Article
Language:English
Published: SAGE Publishing 2020-02-01
Series:Cancer Informatics
Online Access:https://doi.org/10.1177/1176935120907399
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spelling doaj-33f9892188bd431f9c20693a8c0f08782020-11-25T03:39:13ZengSAGE PublishingCancer Informatics1176-93512020-02-011910.1177/1176935120907399A Pan-Cancer and Polygenic Bayesian Hierarchical Model for the Effect of Somatic Mutations on SurvivalSarah Samorodnitsky0Katherine A Hoadley1Eric F Lock2Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN, USADepartment of Genetics, Computational Medicine Program, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USADivision of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN, USAWe built a novel Bayesian hierarchical survival model based on the somatic mutation profile of patients across 50 genes and 27 cancer types. The pan-cancer quality allows for the model to “borrow” information across cancer types, motivated by the assumption that similar mutation profiles may have similar (but not necessarily identical) effects on survival across different tissues of origin or tumor types. The effect of a mutation at each gene was allowed to vary by cancer type, whereas the mean effect of each gene was shared across cancers. Within this framework, we considered 4 parametric survival models (normal, log-normal, exponential, and Weibull), and we compared their performance via a cross-validation approach in which we fit each model on training data and estimate the log-posterior predictive likelihood on test data. The log-normal model gave the best fit, and we investigated the partial effect of each gene on survival via a forward selection procedure. Through this we determined that mutations at TP53 and FAT4 were together the most useful for predicting patient survival. We validated the model via simulation to ensure that our algorithm for posterior computation gave nominal coverage rates. The code used for this analysis can be found at https://github.com/sarahsamorodnitsky/Pan-Cancer-Survival-Modeling.git , and the results are summarized at http://ericfrazerlock.com/surv_figs/SurvivalDisplay.html .https://doi.org/10.1177/1176935120907399
collection DOAJ
language English
format Article
sources DOAJ
author Sarah Samorodnitsky
Katherine A Hoadley
Eric F Lock
spellingShingle Sarah Samorodnitsky
Katherine A Hoadley
Eric F Lock
A Pan-Cancer and Polygenic Bayesian Hierarchical Model for the Effect of Somatic Mutations on Survival
Cancer Informatics
author_facet Sarah Samorodnitsky
Katherine A Hoadley
Eric F Lock
author_sort Sarah Samorodnitsky
title A Pan-Cancer and Polygenic Bayesian Hierarchical Model for the Effect of Somatic Mutations on Survival
title_short A Pan-Cancer and Polygenic Bayesian Hierarchical Model for the Effect of Somatic Mutations on Survival
title_full A Pan-Cancer and Polygenic Bayesian Hierarchical Model for the Effect of Somatic Mutations on Survival
title_fullStr A Pan-Cancer and Polygenic Bayesian Hierarchical Model for the Effect of Somatic Mutations on Survival
title_full_unstemmed A Pan-Cancer and Polygenic Bayesian Hierarchical Model for the Effect of Somatic Mutations on Survival
title_sort pan-cancer and polygenic bayesian hierarchical model for the effect of somatic mutations on survival
publisher SAGE Publishing
series Cancer Informatics
issn 1176-9351
publishDate 2020-02-01
description We built a novel Bayesian hierarchical survival model based on the somatic mutation profile of patients across 50 genes and 27 cancer types. The pan-cancer quality allows for the model to “borrow” information across cancer types, motivated by the assumption that similar mutation profiles may have similar (but not necessarily identical) effects on survival across different tissues of origin or tumor types. The effect of a mutation at each gene was allowed to vary by cancer type, whereas the mean effect of each gene was shared across cancers. Within this framework, we considered 4 parametric survival models (normal, log-normal, exponential, and Weibull), and we compared their performance via a cross-validation approach in which we fit each model on training data and estimate the log-posterior predictive likelihood on test data. The log-normal model gave the best fit, and we investigated the partial effect of each gene on survival via a forward selection procedure. Through this we determined that mutations at TP53 and FAT4 were together the most useful for predicting patient survival. We validated the model via simulation to ensure that our algorithm for posterior computation gave nominal coverage rates. The code used for this analysis can be found at https://github.com/sarahsamorodnitsky/Pan-Cancer-Survival-Modeling.git , and the results are summarized at http://ericfrazerlock.com/surv_figs/SurvivalDisplay.html .
url https://doi.org/10.1177/1176935120907399
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