Evidence map›Paper›PMID 31797615›Full record

ArticlePacific Symposium on Biocomputing. Pacific Symposium on Biocomputing2020

Improving survival prediction using a novel feature selection and feature reduction framework based on the integration of clinical and molecular data.

Lisa Neums, Richard Meier, Devin C Koestler, Jeffrey A Thompson

Abstract read
In one paragraph

Article in Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Observational
  3. Article
  4. Article
  5. 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

4 authors.

Lisa NeumsDepartment of Biostatistics and Data Science, University of Kansas Medical Center, 3901 Rainbow Blvd., Kansas City, KS 66160, USA.
Richard Meier
Devin C Koestler
Jeffrey A Thompson

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Douglas E Wright · 2012 to 2026
$63.0M
Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ROY A. JENSEN · 2012 to 2026
$40.1M
Using Integrated Omics to Identify Dysfunctional Genetic Mechanisms Influencing Schizophrenia and Sleep DisturbancesP20GM130423 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Kalyani Pyaram, Steven Allan Soper · 2019 to 2026
$21.5M
NCI NIH HHS P30 CA168524NIGMS NIH HHS P20 GM103418NIGMS NIH HHS P20 GM130423
6 · The paper itself

Abstract

The accurate prediction of a cancer patient's risk of progression or death can guide clinicians in the selection of treatment and help patients in planning personal affairs. Predictive models based on patient-level data represent a tool for determining risk. Ideally, predictive models will use multiple sources of data (e.g., clinical, demographic, molecular, etc.). However, there are many challenges associated with data integration, such as overfitting and redundant features. In this paper we aim to address those challenges through the development of a novel feature selection and feature reduction framework that can handle correlated data. Our method begins by computing a survival distance score for gene expression, which in combination with a score for clinical independence, results in the selection of highly predictive genes that are non-redundant with clinical features. The survival distance score is a measure of variation of gene expression over time, weighted by the variance of the gene expression over all patients. Selected genes, in combination with clinical data, are used to build a predictive model for survival. We benchmark our approach against commonly used methods, namely lasso- as well as ridge-penalized Cox proportional hazards models, using three publicly available cancer data sets: kidney cancer (521 samples), lung cancer (454 samples) and bladder cancer (335 samples). Across all data sets, our approach built on the training set outperformed the clinical data alone in the test set in terms of predictive power with a c.Index of 0.773 vs 0.755 for kidney cancer, 0.695 vs 0.664 for lung cancer and 0.648 vs 0.636 for bladder cancer. Further, we were able to show increased predictive performance of our method compared to lasso-penalized models fit to both gene expression and clinical data, which had a c.Index of 0.767, 0.677, and 0.645, as well as increased or comparable predictive power compared to ridge models, which had a c.Index of 0.773, 0.668 and 0.650 for the kidney, lung, and bladder cancer data sets, respectively. Therefore, our score for clinical independence improves prognostic performance as compared to modeling approaches that do not consider combining non-redundant data. Future work will concentrate on optimizing the survival distance score in order to achieve improved results for all types of cancer.

Indexed as

Kidney NeoplasmsLung NeoplasmsComputational BiologyHumansProportional Hazards Models

Identifiers

PMID31797615
PMCPMC6941850

What OpenQuestion holds

Textmetadata
LicenceTDM
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.