Evidence map›Paper›PMID 34514927›Full record

ArticleCancer investigation2021

Impervious to Randomness: Confounding and Selection Biases in Randomized Clinical Trials.

Pavlos Msaouel

Open access · greenAbstract read
In one paragraph

Article in Cancer investigation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.1field-weighted citation impact, top 7% of its field
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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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  5. Article
  6. Review
  7. The Big Data Paradox in Clinical Practice.Cancer investigation · 2022
    Article
  8. Article
  9. Article
  10. 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

1 author at 1 institution in 1 country.

Pavlos MsaouelDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0001-6505-8308
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

The random allocation of therapies in randomized clinical trials is a powerful tool that removes all confounding biases that can affect treatment assignment. However, confounders influencing mediators of the treatment effect are unaffected by randomization and should be considered during trial design and statistical modeling.Examples of such mediators include biomarkers predictive of response to targeted therapies in oncology. Patient selection for such biomarkers is prudent in clinical trials. Conversely, prognostic information on outcome heterogeneity can be derived from observational datasets that include more representative populations. The fusion of experimental and observational data can then allow patient-specific inferences.

Indexed as

Selection BiasHumansRandom AllocationRandomized Controlled Trials as TopicConfoundingdirected acyclic graphsmediation analysisrepresentativenessselection bias

Identifiers

PMID34514927
PMCPMC12268927
OpenAlexW3200278087

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.