Abstract

BackgroundOne of the most important objectives of the clinical cancer research is to diagnose cancer more accurately based on the patients’ gene expression profiles. Both Cox proportional hazards model (Cox) and accelerated failure time model (AFT) have been widely adopted to the high risk and low risk classification or survival time prediction for the patients’ clinical treatment. Nevertheless, two main dilemmas limit the accuracy of these prediction methods. One is that the small sample size and censored data remain a bottleneck for training robust and accurate Cox classification model. In addition to that, similar phenotype tumours and prognoses are actually completely different diseases at the genotype and molecular level. Thus, the utility of the AFT model for the survival time prediction is limited when such biological differences of the diseases have not been previously identified.MethodsTo try to overcome these two main dilemmas, we proposed a novel semi-supervised learning method based on the Cox and AFT models to accurately predict the treatment risk and the survival time of the patients. Moreover, we adopted the efficient L1/2 regularization approach in the semi-supervised learning method to select the relevant genes, which are significantly associated with the disease.ResultsThe results of the simulation experiments show that the semi-supervised learning model can significant improve the predictive performance of Cox and AFT models in survival analysis. The proposed procedures have been successfully applied to four real microarray gene expression and artificial evaluation datasets.ConclusionsThe advantages of our proposed semi-supervised learning method include: 1) significantly increase the available training samples from censored data; 2) high capability for identifying the survival risk classes of patient in Cox model; 3) high predictive accuracy for patients’ survival time in AFT model; 4) strong capability of the relevant biomarker selection. Consequently, our proposed semi-supervised learning model is one more appropriate tool for survival analysis in clinical cancer research.

Highlights

  • One of the most important objectives of the clinical cancer research is to diagnose cancer more accurately based on the patients’ gene expression profiles

  • We propose a novel semi-supervised learning method based on the combination of Cox and accelerated failure time model (AFT) models with L1/2 regularization for high-dimensional and low sample size biological data

  • Step 3: Censoring time point yi′(i = 1,...n) is obtained from an random distribution E (θ), where θ is determined by specify censoring rate

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Summary

Introduction

One of the most important objectives of the clinical cancer research is to diagnose cancer more accurately based on the patients’ gene expression profiles Both Cox proportional hazards model (Cox) and accelerated failure time model (AFT) have been widely adopted to the high risk and low risk classification or survival time prediction for the patients’ clinical treatment. An important objective of clinical cancer research is to develop tools to accurately predict the survival time and risk profile of patients based on the DNA microarray data and various clinical parameters. There are several existing techniques in the literature for performing this type of survival analysis Among of them, both Cox proportional hazards model (Cox) [1] and the accelerated failure time model (AFT) [2] have been widely used. We believe any attempt to improve the accuracy of survival analysis method has to compromise between these two dilemmas: The small sample size and censored survival data versus high dimensional covariates dilemma in Cox model

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