Evidence map›Paper›PMID 32183709›Full record

ArticleBMC bioinformatics2020

A deep learning-based framework for lung cancer survival analysis with biomarker interpretation.

Lei Cui, Hansheng Li, Wenli Hui, Sitong Chen, Lin Yang, Yuxin Kang, Qirong Bo, Jun Feng

Abstract readEvaluation Study
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Lei CuiDepartment of Information Science and Technology, Northwest University, Xi'an, China.
Hansheng LiDepartment of Information Science and Technology, Northwest University, Xi'an, China.
Wenli HuiThe College of Life Sciences, Northwest University, Xi'an, China.
Sitong ChenThe College of Life Sciences, Northwest University, Xi'an, China.
Lin YangThe College of Life Sciences, Northwest University, Xi'an, China.
Yuxin KangDepartment of Information Science and Technology, Northwest University, Xi'an, China.
Qirong BoDepartment of Information Science and Technology, Northwest University, Xi'an, China.
Jun FengDepartment of Information Science and Technology, Northwest University, Xi'an, China. fengjun@nwu.edu.cn.ORCID http://orcid.org/0000-0002-0706-2103

Funding

Major Program of National Natural Science Foundation of China 81727802National Key Research and Development Program of China under grant 2017YFB1002504National Natural Science Foundation of China 61701404
6 · The paper itself

Abstract

backgroundLung cancer is the leading cause of cancer-related deaths in both men and women in the United States, and it has a much lower five-year survival rate than many other cancers. Accurate survival analysis is urgently needed for better disease diagnosis and treatment management.

resultsIn this work, we propose a survival analysis system that takes advantage of recently emerging deep learning techniques. The proposed system consists of three major components. 1) The first component is an end-to-end cellular feature learning module using a deep neural network with global average pooling. The learned cellular representations encode high-level biologically relevant information without requiring individual cell segmentation, which is aggregated into patient-level feature vectors by using a locality-constrained linear coding (LLC)-based bag of words (BoW) encoding algorithm. 2) The second component is a Cox proportional hazards model with an elastic net penalty for robust feature selection and survival analysis. 3) The third commponent is a biomarker interpretation module that can help localize the image regions that contribute to the survival model's decision. Extensive experiments show that the proposed survival model has excellent predictive power for a public (i.e., The Cancer Genome Atlas) lung cancer dataset in terms of two commonly used metrics: log-rank test (p-value) of the Kaplan-Meier estimate and concordance index (c-index).

conclusionsIn this work, we have proposed a segmentation-free survival analysis system that takes advantage of the recently emerging deep learning framework and well-studied survival analysis methods such as the Cox proportional hazards model. In addition, we provide an approach to visualize the discovered biomarkers, which can serve as concrete evidence supporting the survival model's decision.

Indexed as

Survival AnalysisAlgorithmsBiomarkersDeep LearningFemaleHumansKaplan-Meier EstimateLung NeoplasmsMaleNeural Networks, ComputerProportional Hazards ModelsBiomarkersCell detectionDeep learningFeature learningSurvival analysis

Identifiers

PMID32183709
PMCPMC7079513

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.