Evidence map›Paper›PMID 33769304›Full record

ArticleJMIR medical informatics2021

Accuracy of an Artificial Intelligence System for Cancer Clinical Trial Eligibility Screening: Retrospective Pilot Study.

Tufia Haddad, Jane M Helgeson, Katharine E Pomerleau, Anita M Preininger, M Christopher Roebuck, Irene Dankwa-Mullan, Gretchen Purcell Jackson, Matthew P Goetz

Open access · goldAbstract read
In one paragraph

Article in JMIR medical informatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. AI-based augmentation of oncology clinical trials.Nature reviews. Clinical oncology · 2026
    Review
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  19. A Deployed Online Reinforcement Learning Algorithm In An Oral Health Clinical Trial.Proceedings of the ... AAAI Conference on Artificial Intelligence. AAAI Conference on Artificial Intelligence · 2025
    Article
  20. Artificial intelligence for optimizing recruitment and retention in clinical trials: a scoping review.Journal of the American Medical Informatics Association : JAMIA · 2024
    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 at 2 institutions in 1 country.

Tufia HaddadMayo Clinic, Rochester, MN, United States.ORCID https://orcid.org/0000-0001-8226-3581
Jane M HelgesonMayo Clinic, Rochester, MN, United States.ORCID https://orcid.org/0000-0001-7375-3706
Katharine E PomerleauMayo Clinic, Rochester, MN, United States.ORCID https://orcid.org/0000-0002-8803-1850
Anita M PreiningerIBM Watson Health, Cambridge, ME, United States.ORCID https://orcid.org/0000-0001-8011-9391
M Christopher RoebuckRxEconomics LLC, Hunt Valley, MD, United States.ORCID https://orcid.org/0000-0003-4102-4925
Irene Dankwa-MullanIBM Watson Health, Cambridge, ME, United States.ORCID https://orcid.org/0000-0002-6792-3497
Gretchen Purcell JacksonIBM Watson Health, Cambridge, ME, United States.ORCID https://orcid.org/0000-0002-3242-8058
Matthew P GoetzMayo Clinic, Rochester, MN, United States.ORCID https://orcid.org/0000-0002-4383-270X
Mayo Clinic in Arizona · USIBM (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundScreening patients for eligibility for clinical trials is labor intensive. It requires abstraction of data elements from multiple components of the longitudinal health record and matching them to inclusion and exclusion criteria for each trial. Artificial intelligence (AI) systems have been developed to improve the efficiency and accuracy of this process.

objectiveThis study aims to evaluate the ability of an AI clinical decision support system (CDSS) to identify eligible patients for a set of clinical trials.

methodsThis study included the deidentified data from a cohort of patients with breast cancer seen at the medical oncology clinic of an academic medical center between May and July 2017 and assessed patient eligibility for 4 breast cancer clinical trials. CDSS eligibility screening performance was validated against manual screening. Accuracy, sensitivity, specificity, positive predictive value, and negative predictive value for eligibility determinations were calculated. Disagreements between manual screeners and the CDSS were examined to identify sources of discrepancies. Interrater reliability between manual reviewers was analyzed using Cohen (pairwise) and Fleiss (three-way) κ, and the significance of differences was determined by Wilcoxon signed-rank test.

resultsIn total, 318 patients with breast cancer were included. Interrater reliability for manual screening ranged from 0.60-0.77, indicating substantial agreement. The overall accuracy of breast cancer trial eligibility determinations by the CDSS was 87.6%. CDSS sensitivity was 81.1% and specificity was 89%.

conclusionsThe AI CDSS in this study demonstrated accuracy, sensitivity, and specificity of greater than 80% in determining the eligibility of patients for breast cancer clinical trials. CDSSs can accurately exclude ineligible patients for clinical trials and offer the potential to increase screening efficiency and accuracy. Additional research is needed to explore whether increased efficiency in screening and trial matching translates to improvements in trial enrollment, accruals, feasibility assessments, and cost.

Indexed as

artificial intelligencebreast cancerclinical decision support systemclinical trial matchingclinical trialseligibilitymachine learningscreening

Identifiers

PMID33769304
PMCPMC8088869
OpenAlexW3135855542

What OpenQuestion holds

Textmetadata
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.