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Deep learning-based cancer survival prognosis from RNA-seq data: approaches and evaluations
Zhi Huang1,2,3, Travis S Johnson2,4, Zhi Han2
1School of Electrical and Computer Engineering, Purdue University, West Lafayette, IN, 47907, USA.
BMC Medical Genomics
|April 4, 2020
Summary
Deep learning models, including Cox-nnet, DeepSurv, and AECOX, accurately predict cancer patient survival using transcriptomic data. Prognosis accuracy correlates with overall survival and tumor mutation burden across various cancers.
Area of Science:
- Computational Biology
- Bioinformatics
- Machine Learning in Oncology
Background:
- Deep Learning (DL) models, initially for image processing, are now advancing medical research, particularly in cancer patient survival prognosis.
- DL-based Cox proportional hazards models utilize transcriptomic data for predicting cancer survival outcomes.
Purpose of the Study:
- To conduct a comprehensive analysis of DL-based survival prognosis models across various TCGA (The Cancer Genome Atlas) cancers.
- To evaluate and compare the performance of established DL models (Cox-nnet, DeepSurv) and a novel method (AECOX).
Main Methods:
- Utilized transcriptomic data from TCGA cancers.
- Applied and evaluated Deep Learning models: Cox-nnet, DeepSurv, and AECOX (AutoEncoder with Cox regression network).
- Assessed model performance using concordance index and log-rank test p-values.
Main Results:
- All evaluated DL models demonstrated competitive performance across 12 cancer types.
- Lower-dimensional representations from DL models' hidden layers facilitate feature reduction and visualization.
- Prognosis accuracy showed a negative correlation with overall survival and tumor mutation burden (TMB), indicating a link between survival, TMB, and prediction accuracy.
Conclusions:
- DL algorithms outperform traditional machine learning models in cancer prognosis.
- While model performance (concordance index) was comparable across DL methods, it varied significantly among different cancer types.
- Findings illuminate the interplay between patient characteristics, survival data, and predictive model learnability on a pan-cancer scale.
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