Evidence map›Paper›PMID 32881987›Full record

ArticlePloS one2020

Computational approaches to support comparative analysis of multiparametric tests: Modelling versus Training.

John M S Bartlett, Jane Bayani, Elizabeth N Kornaga, Patrick Danaher, Cheryl Crozier, Tammy Piper, Cindy Q Yao, Janet A Dunn, Paul C Boutros, Robert C Stein and 1 more

Abstract readComparative Study
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Trial
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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

11 authors.

John M S BartlettDiagnostic Development, Ontario Institute for Cancer Research, Toronto, Ontario, Canada.ORCID 0000-0002-0347-3888
Jane BayaniDiagnostic Development, Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
Elizabeth N KornagaTom Baker Cancer Centre, Calgary, Alberta, Canada.
Patrick DanaherDiagnostic Development, Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
Cheryl CrozierDiagnostic Development, Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
Tammy PiperEdinburgh Cancer Research Centre, Edinburgh, United Kingdom.
Cindy Q YaoComputational Biology Program, Ontario Institute for Cancer Research, Toronto, Ontario, Canada.
Janet A DunnWarwick Medical School, University of Warwick, Coventry, United Kingdom.
Paul C BoutrosComputational Biology Program, Ontario Institute for Cancer Research, Toronto, Ontario, Canada.ORCID 0000-0003-0553-7520
Robert C SteinUCL (University College London) and National Institute for Health Research University College London Hospitals Biomedical Research Centre, London, United Kingdom.ORCID 0000-0003-2969-0415
OPTIMA Trial Management Group

Funding

UCLA SPORE in Brain CancerP50CA211015 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI David A. Nathanson · 2017 to 2026
$25.2M
CIHRDepartment of Health 10/34/01NCI NIH HHS P50 CA211015
6 · The paper itself

Abstract

Multiparametric assays for risk stratification are widely used in the management of breast cancer, with applications being developed for a number of other cancer settings. Recent data from multiple sources suggests that different tests may provide different risk estimates at the individual patient level. There is an increasing need for robust methods to support cost effective comparisons of test performance in multiple settings. The derivation of similar risk classifications using genes comprising the following multi-parametric tests Oncotype DX® (Genomic Health.), Prosigna™ (NanoString Technologies, Inc.), MammaPrint® (Agendia Inc.) was performed using different computational approaches. Results were compared to the actual test results. Two widely used approaches were applied, firstly computational "modelling" of test results using published algorithms and secondly a "training" approach which used reference results from the commercially supplied tests. We demonstrate the potential for errors to arise when using a "modelling" approach without reference to real world test results. Simultaneously we show that a "training" approach can provide a highly cost-effective solution to the development of real-world comparisons between different multigene signatures. Comparisons between existing multiparametric tests is challenging, and evidence on discordance between tests in risk stratification presents further dilemmas. We present an approach, modelled in breast cancer, which can provide health care providers and researchers with the potential to perform robust and meaningful comparisons between multigene tests in a cost-effective manner. We demonstrate that whilst viable estimates of gene signatures can be derived from modelling approaches, in our study using a training approach allowed a close approximation to true signature results.

Indexed as

Breast NeoplasmsComputer SimulationCost-Benefit AnalysisFemaleGene Expression ProfilingGenomicsHumansPrognosisRandomized Controlled Trials as Topic

Identifiers

PMID32881987
PMCPMC7470374

What OpenQuestion holds

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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.