Evidence map›Paper›PMID 26932592›Full record

ArticleBMC medical genomics2016

Cancer survival analysis using semi-supervised learning method based on Cox and AFT models with L1/2 regularization.

Yong Liang, Hua Chai, Xiao-Ying Liu, Zong-Ben Xu, Hai Zhang, Kwong-Sak Leung

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Article in BMC medical genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

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11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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  4. Integrating molecular interactions and gene expression to identify biomarkers and network modules of chronic obstructive pulmonary disease.Technology and health care : official journal of the European Society for Engineering and Medicine · 2022
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yong LiangState Key Laboratory of Quality Research in Chinese Medicines & Faculty of Information Technology, Macau University of Science and Technology, Macau, China. yliang@must.edu.mo.
Hua ChaiState Key Laboratory of Quality Research in Chinese Medicines & Faculty of Information Technology, Macau University of Science and Technology, Macau, China.
Xiao-Ying LiuState Key Laboratory of Quality Research in Chinese Medicines & Faculty of Information Technology, Macau University of Science and Technology, Macau, China.
Zong-Ben XuFaculty of Science, Xi'an Jiaotong University, Xi'an, China.
Hai ZhangFaculty of Science, Xi'an Jiaotong University, Xi'an, China.
Kwong-Sak LeungDepartment of Computer Science and Engineering, The Chinese University of HongKong, HongKong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Computer SimulationDatabases as TopicGene Expression Regulation, NeoplasticHumansModels, TheoreticalNeoplasmsOligonucleotide Array Sequence AnalysisProportional Hazards ModelsSurvival Analysis

Identifiers

PMID26932592
PMCPMC4774162

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.