Evidence map›Paper›PMID 29880025›Full record

ArticleBiology direct2018

Predicting clinical outcome of neuroblastoma patients using an integrative network-based approach.

Léon-Charles Tranchevent, Petr V Nazarov, Tony Kaoma, Georges P Schmartz, Arnaud Muller, Sang-Yoon Kim, Jagath C Rajapakse, Francisco Azuaje

Abstract read
In one paragraph

Article in Biology direct, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
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  4. Article
  5. Article
  6. Liquid biopsies and cancer omics.Cell death discovery · 2020
    Review
  7. Cancer predictive studies.Biology direct · 2020
    Review
  8. Article
  9. 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.

Léon-Charles TrancheventProteome and Genome Research Unit, Department of Oncology, Luxembourg Institute of Health, 1A-B, rue Thomas Edison, Strassen, L-1445, Luxembourg.ORCID 0000-0002-1257-4824
Petr V NazarovProteome and Genome Research Unit, Department of Oncology, Luxembourg Institute of Health, 1A-B, rue Thomas Edison, Strassen, L-1445, Luxembourg.
Tony KaomaProteome and Genome Research Unit, Department of Oncology, Luxembourg Institute of Health, 1A-B, rue Thomas Edison, Strassen, L-1445, Luxembourg.
Georges P SchmartzProteome and Genome Research Unit, Department of Oncology, Luxembourg Institute of Health, 1A-B, rue Thomas Edison, Strassen, L-1445, Luxembourg.
Arnaud MullerProteome and Genome Research Unit, Department of Oncology, Luxembourg Institute of Health, 1A-B, rue Thomas Edison, Strassen, L-1445, Luxembourg.
Sang-Yoon KimProteome and Genome Research Unit, Department of Oncology, Luxembourg Institute of Health, 1A-B, rue Thomas Edison, Strassen, L-1445, Luxembourg.
Jagath C RajapakseBioinformatics Research Center, School of Computer Science and Engineering, Nanyang Technological University, Singapore, Singapore.
Francisco AzuajeProteome and Genome Research Unit, Department of Oncology, Luxembourg Institute of Health, 1A-B, rue Thomas Edison, Strassen, L-1445, Luxembourg. Francisco.Azuaje@lih.lu.

Funding

Fonds National de la Recherche (FNR), Luxembourg SINGALUN projectTier-2 grant, Ministry of Education, Singapore MOE2016-T2-1-029
6 · The paper itself

Abstract

backgroundOne of the main current challenges in computational biology is to make sense of the huge amounts of multidimensional experimental data that are being produced. For instance, large cohorts of patients are often screened using different high-throughput technologies, effectively producing multiple patient-specific molecular profiles for hundreds or thousands of patients.

resultsWe propose and implement a network-based method that integrates such patient omics data into Patient Similarity Networks. Topological features derived from these networks were then used to predict relevant clinical features. As part of the 2017 CAMDA challenge, we have successfully applied this strategy to a neuroblastoma dataset, consisting of genomic and transcriptomic data. In particular, we observe that models built on our network-based approach perform at least as well as state of the art models. We furthermore explore the effectiveness of various topological features and observe, for instance, that redundant centrality metrics can be combined to build more powerful models.

conclusionWe demonstrate that the networks inferred from omics data contain clinically relevant information and that patient clinical outcomes can be predicted using only network topological data. REVIEWERS: This article was reviewed by Yang-Yu Liu, Tomislav Smuc and Isabel Nepomuceno.

Indexed as

AlgorithmsComputational BiologyGene Regulatory NetworksGenomicsHumansNeuroblastomaBiological networksNetwork-based methodsNetwork topology

Identifiers

PMID29880025
PMCPMC5992838

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Registered trials

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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.