Evidence map›Paper›PMID 24766212›Full record

ArticleBiometrics2014

Integrative analysis of prognosis data on multiple cancer subtypes.

Jin Liu, Jian Huang, Yawei Zhang, Qing Lan, Nathaniel Rothman, Tongzhang Zheng, Shuangge Ma

Abstract read
In one paragraph

Article in Biometrics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Integrative sparse partial least squares.Statistics in medicine · 2021
    Article
  6. Article
  7. GRIA: Graphical Regularization for Integrative Analysis.Proceedings of the ... SIAM International Conference on Data Mining. SIAM International Conference on Data Mining · 2020
    Article
  8. Simultaneous Covariance Inference for Multimodal Integrative Analysis.Journal of the American Statistical Association · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Integrative Analysis of "-Omics" Data Using Penalty Functions.Wiley interdisciplinary reviews. Computational statistics
    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

7 authors.

Jin LiuDivision of Epidemiology and Biostatistics, UIC School of Public Health, Chicago, Illinois, U.S.A.
Jian HuangDepartment of Statistics & Actuarial Science, University of Iowa, Iowa City, Iowa, U.S.A.
Yawei ZhangSchool of Public Health, Yale University, New Haven, Connecticut, U.S.A.
Qing LanDivision of Cancer Epidemiology and Genetics, NCI, NIH, Bethesda, Maryland, U.S.A.
Nathaniel RothmanDivision of Cancer Epidemiology and Genetics, NCI, NIH, Bethesda, Maryland, U.S.A.
Tongzhang ZhengSchool of Public Health, Yale University, New Haven, Connecticut, U.S.A.
Shuangge MaSchool of Public Health, Yale University, New Haven, Connecticut, U.S.A.

Funding

Predicting Adjuvant Chemotherapy Response in Lung CancerR01CA152301 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI XIE, YANG · 2010 to 2014
$1.5M
Novel Methods for Integrative Analysis of Cancer Genomic DataR01CA142774 · NCI · YALE UNIVERSITY · PI MA, SHUANGGE · 2010 to 2013
$1.3M
Robust rank-based methods and detection of GXE in cancer etiology and survivalR21CA165923 · NCI · YALE UNIVERSITY · PI MA, SHUANGGE, ZHANG, YAWEI · 2012 to 2014
$421k
NCI NIH HHS CA142774NCI NIH HHS CA152301NCI NIH HHS CA165923NCI NIH HHS R01 CA142774NCI NIH HHS R01 CA152301NCI NIH HHS R21 CA165923
6 · The paper itself

Abstract

In cancer research, profiling studies have been extensively conducted, searching for genes/SNPs associated with prognosis. Cancer is diverse. Examining the similarity and difference in the genetic basis of multiple subtypes of the same cancer can lead to a better understanding of their connections and distinctions. Classic meta-analysis methods analyze each subtype separately and then compare analysis results across subtypes. Integrative analysis methods, in contrast, analyze the raw data on multiple subtypes simultaneously and can outperform meta-analysis methods. In this study, prognosis data on multiple subtypes of the same cancer are analyzed. An AFT (accelerated failure time) model is adopted to describe survival. The genetic basis of multiple subtypes is described using the heterogeneity model, which allows a gene/SNP to be associated with prognosis of some subtypes but not others. A compound penalization method is developed to identify genes that contain important SNPs associated with prognosis. The proposed method has an intuitive formulation and is realized using an iterative algorithm. Asymptotic properties are rigorously established. Simulation shows that the proposed method has satisfactory performance and outperforms a penalization-based meta-analysis method and a regularized thresholding method. An NHL (non-Hodgkin lymphoma) prognosis study with SNP measurements is analyzed. Genes associated with the three major subtypes, namely DLBCL, FL, and CLL/SLL, are identified. The proposed method identifies genes that are different from alternatives and have important implications and satisfactory prediction performance.

Indexed as

Data Interpretation, StatisticalMeta-Analysis as TopicSurvival AnalysisGenetic MarkersGenetic Predisposition to DiseaseHumansNeoplasmsPolymorphism, Single NucleotidePrevalencePrognosisReproducibility of ResultsRisk AssessmentSensitivity and SpecificitySystems IntegrationGenetic MarkersCancer prognosisIntegrative analysisMarker identificationPenalization

Identifiers

PMID24766212
PMCPMC4209207

What OpenQuestion holds

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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.