Evidence map›Paper›PMID 34227170›Full record

ArticlePharmacoepidemiology and drug safety2022

Differential frequency in imaging-based outcome measurement: Bias in real-world oncology comparative-effectiveness studies.

Blythe J S Adamson, Xinran Ma, Sandra D Griffith, Elizabeth M Sweeney, Somnath Sarkar, Ariel B Bourla

Abstract read
In one paragraph

Article in Pharmacoepidemiology and drug safety, 2022. 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
–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

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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.

  1. Article
  2. Article
  3. Real-World Data and Causal Machine Learning to Enhance Drug Development.Therapeutic innovation & regulatory science · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Review
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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

6 authors.

Blythe J S AdamsonFlatiron Health, Inc., New York, New York, USA.ORCID 0000-0003-4251-2912
Xinran MaFlatiron Health, Inc., New York, New York, USA.ORCID 0000-0002-7138-2638
Sandra D GriffithFlatiron Health, Inc., New York, New York, USA.
Elizabeth M SweeneyFlatiron Health, Inc., New York, New York, USA.
Somnath SarkarFlatiron Health, Inc., New York, New York, USA.ORCID 0000-0002-8158-3847
Ariel B BourlaFlatiron Health, Inc., New York, New York, USA.ORCID 0000-0002-9838-0544

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundComparative-effectiveness studies using real-world data (RWD) can be susceptible to surveillance bias. In solid tumor oncology studies, analyses of endpoints such as progression-free survival (PFS) are based on progression events detected by imaging assessments. This study aimed to evaluate the potential bias introduced by differential imaging assessment frequency when using electronic health record (EHR)-derived data to investigate the comparative effectiveness of cancer therapies.

methodsUsing a nationwide de-identified EHR-derived database, we first analyzed imaging assessment frequency patterns in patients diagnosed with advanced non-small cell lung cancer (aNSCLC). We used those RWD inputs to develop a discrete event simulation model of two treatments where disease progression was the outcome and PFS was the endpoint. Using this model, we induced bias with differential imaging assessment timing and quantified its effect on observed versus true treatment effectiveness. We assessed percent bias in the estimated hazard ratio (HR).

resultsThe frequency of assessments differed by cancer treatment types. In simulated comparative-effectiveness studies, PFS HRs estimated using real-world imaging assessment frequencies differed from the true HR by less than 10% in all scenarios (range: 0.4% to -9.6%). The greatest risk of biased effect estimates was found comparing treatments with widely different imaging frequencies, most exaggerated in disease settings where time to progression is very short.

conclusionsThis study provided evidence that the frequency of imaging assessments to detect disease progression can differ by treatment type in real-world patients with cancer and may induce some bias in comparative-effectiveness studies in some situations.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsBiasHumansProgression-Free Survivalcancercomparative-effectiveness analysisimaging assessment timingmeasurement biasprogression-free survival (PFS)real-word data (RWD)scan timingsimulation modeling

Identifiers

PMID34227170
PMCPMC9290806

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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.