Evidence map›Paper›PMID 24000377›Full record

ArticleClinical trials (London, England)2013

Development of omics-based clinical tests for prognosis and therapy selection: the challenge of achieving statistical robustness and clinical utility.

Lisa M McShane, Mei-Yin C Polley

Registry-linked trialAbstract read
In one paragraph

Article in Clinical trials (London, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05697198 (PRospective REgistry of Advanced Stage CancER), which is not on this 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.

NCT05697198 completednot on this mapstarted 2021, after this paper: background citation

PRospective REgistry of Advanced Stage CancER (PREFER) Patients to Assess Prevalence of Actionable Biomarkers and Driver Mutations Using the OmniSeq Test and Creation of a Biobank from Community Cancer Clinics in the United States to Address Disparities in Precision Medicine

Typeobservational_patient_registrySponsorLabcorp Corporation of America Holdings, IncRan2021 to 2024Enrolled1,429ConditionsLung Cancer, Ovarian Cancer, Uterine Cancer, Colorectal CancerArmsOmniSeq Test
3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Precision medicine and metabolic syndrome.ARYA atherosclerosis · 2022
    Review
  7. Statistical Considerations in the Evaluation of Continuous Biomarkers.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2021
    Review
  8. Article
  9. Review
  10. Biomarker development for axial spondyloarthritis.Nature reviews. Rheumatology · 2020
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Prognosis vs Treatment Interaction.JNCI cancer spectrum · 2018
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

2 authors.

Lisa M McShaneBiometric Research Branch, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, MD, USA.
Mei-Yin C Polley

Funding

Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

backgroundMany articles have been published in biomedical journals reporting on the development of prognostic and therapy-guiding biomarkers or predictors developed from high-dimensional data generated by omics technologies. Few of these tests have advanced to routine clinical use. PURPOSE: We discuss statistical issues in the development and evaluation of prognostic and therapy-guiding biomarkers and omics-based tests.

methodsConcepts relevant to the development and evaluation of prognostic and therapy-guiding clinical tests are illustrated through discussion and examples. Some differences between statistical approaches for test evaluation and therapy evaluation are explained. The additional complexities introduced in the evaluation of omics-based tests are highlighted.

resultsDistinctions are made between clinical validity of a test and clinical utility. To establish clinical utility for prognostic tests, it is explained why absolute risk should be evaluated in addition to relative risk measures. The critical role of an appropriate control group is emphasized for evaluation of therapy-guiding tests. Common pitfalls in the development and evaluation of tests generated from high-dimensional omics data such as model overfitting and inappropriate methods for test performance evaluation are explained, and proper approaches are suggested. LIMITATIONS: The cited references do not comprise an exhaustive list of useful references on this topic, and a systematic review of the literature was not performed. Instead, a few key points were highlighted and illustrated with examples drawn from the oncology literature.

conclusionsApproaches for the development and statistical evaluation of clinical tests useful for predicting prognosis and selecting therapy differ from standard approaches for therapy evaluation. Proper evaluation requires an understanding of the clinical setting and what information is likely to influence clinical decisions. Specialized expertise relevant to building mathematical predictor models from high-dimensional data is helpful to avoid common pitfalls in the development and evaluation of omics-based tests.

Indexed as

BiomarkersData Interpretation, StatisticalClinical Trials as TopicComputational BiologyHumansPrognosisReproducibility of ResultsBiomarkers

Identifiers

PMID24000377
PMCPMC4410005

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Registered trials

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.